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US20120071496A1 - Aminopyrimidinamides As Pest Control Agents - Google Patents

Aminopyrimidinamides As Pest Control Agents Download PDF

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Publication number
US20120071496A1
US20120071496A1 US13/201,940 US201013201940A US2012071496A1 US 20120071496 A1 US20120071496 A1 US 20120071496A1 US 201013201940 A US201013201940 A US 201013201940A US 2012071496 A1 US2012071496 A1 US 2012071496A1
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United States
Prior art keywords
spp
cyclopropyl
alkyl
group
haloalkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
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US13/201,940
Inventor
Simon MAECHLING
Arnd Voerste
Eva-Maria Franken
Angela Becker
Ulrich Görgens
Mazen Es-Sayed
Markus Heil
Graham Holmwood
Johannes-Rudolf Jansen
Otto Schallner
Ulrich Ebbinghaus-Kintscher
Peter Lümmen
Silvia Cerezo-Galvez
Sachio Kudo
Takashi Hashihayata
Eiichi Shimojo
Teruyuki Ichihara
Masashi Ataka
Katsuhiko Shibuya
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Bayer CropScience AG
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Bayer CropScience AG
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Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of US20120071496A1 publication Critical patent/US20120071496A1/en
Abandoned legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48—Two nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/14—Ectoparasiticides, e.g. scabicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the present application relates to novel aminopyrimidinamides, to processes for their preparation and to their use as pesticides and in particular as insecticides and/or parasiticides.
  • WO 2002/067684 discloses certain pyridylpyrimidines as pesticides. However, they do not meet all demands in a satisfactory manner.
  • novel compounds of the formula (I) have pronounced biological properties and are suitable especially for controlling animal pests, in particular insects, arachnids and nematodes, encountered in agriculture, in forests, in the protection of stored products and materials and in the hygiene sector.
  • the compounds of the formula (I) may, depending on the nature of the substituents, be present as geometrical and/or as optically active isomers or corresponding isomer mixtures or in various tautomeric forms of varying compositions.
  • the invention relates both to the pure isomers and to the isomer mixtures.
  • the compounds of the formula (I) may be present in various polymorphic forms or as mixtures of different polymorphic forms.
  • the invention provides both the pure polymorphs and the polymorph mixtures, and both can be used according to the invention.
  • the formula (I) provides a general definition of the compounds according to the invention.
  • halogen also in radicals such as, for example, haloalkyl
  • halogen is selected from the group consisting of fluorine, chlorine, bromine and iodine, preferably from the group consisting of fluorine, chlorine and bromine
  • heteroaryl or hetaryl is selected from the group consisting of furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,2,5-thiadiazolyl, 1,2,3-thiadia
  • halogen is selected from the group consisting of fluorine, chlorine, bromine and iodine, preferably from the group consisting of fluorine, chlorine and bromine, heteroaryl or hetaryl (also as part of a larger moiety such as, for example, hetarylalkyl) is selected from the group consisting of pyrimidyl, oxadiazolyl, oxazolyl, pyrazinyl, imidazolyl, thiazolyl and furanyl, pyrrolyl, pyrazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4
  • Halogen-substituted radicals for example haloalkyl, are mono- or polysubstituted up to the maximum possible number of substituents.
  • the halogen atoms can be identical or different.
  • halogen represents fluorine, chlorine, bromine and iodine, in particular fluorine, chlorine and bromine,
  • radical definitions or illustrations given above apply both to the end products and, correspondingly, to starting materials and intermediates. These radical definitions can be combined with one another as desired, i.e. including combinations between the given preferred ranges.
  • R′ represents cyclopropyl
  • R 7 represents ethyl
  • R 7 represents CH 2 CF 3 .
  • R 5 represents optionally substituted phenyl.
  • R 5 represents optionally substituted 3-pyridyl.
  • Process 1 for preparing the novel compounds of the formula (I), the compound of the formula (II) used is, for example, 6-(4-chlorophenyl)-N-cyclopropyl-pyrimidine-4,5-diamine and the compound of the formula (III) used is 2-ethylnicotinoyl chloride, Process 1 can be represented by Reaction Scheme I below:
  • This reaction is generally carried out by reacting compounds of the formula (II) with compounds of the formula (III) in the presence of a basic auxiliary in a diluent at a temperature of from ⁇ 40° C. to 120° C.
  • Suitable basic auxiliaries are amines, for example trialkylamines or pyridines. Pyridine may be mentioned by way of example.
  • diluents are advantageously employed in such an amount that the reaction mixture remains readily stirrable during the entire process.
  • Suitable diluents for carrying out the Process 1 according to the invention are organic solvents which are inert under the reaction conditions.
  • halogenated hydrocarbons in particular chlorinated hydrocarbons, such as tetrachloroethylene, tetrachloroethane, dichloropropane, methylene chloride (DCM), dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichloroethylene, pentachloroethane, difluorobenzene, 1,2-dichloroethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene; ethers, such as ethyl propyl ether, methyl tert-butyl ether, n-butyl ether, anisole, phenetole, cyclohexyl methyl ether, dimethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, di-n-buty
  • the products obtained after work-up can be purified in a customary manner by recrystallization, distillation under reduced pressure or column chromatography (cf. also the Preparation Examples).
  • the formula (III) describes the compounds furthermore to be used as starting materials for carrying out Process 1 according to the invention.
  • R 4 has the meanings already mentioned in connection with the description of the compounds of the formula (I) according to the invention.
  • the compound of the formula (IV) used is, for example, N-(4-chloro-6-cyclopropylaminopyrimidin-5-yl)-2-ethylnicotinamide and the compound of the formula (V) is 2,4-dichlorophenylboronic acid, the process can be represented by Reaction Scheme II below;
  • the compound of the formula (IV) is reacted in a suitable diluent, such as, for example, alcohols (for example methanol or ethanol), ethers (for example diethyl ether or dioxane) or water or a mixture of these diluents (for example dioxane/water), if appropriate in the presence of a base and in the presence of suitable palladium catalysts and bases in a temperature range of from ⁇ 20° C. to 120° C. in suitable solvents (Suzuki reaction).
  • a suitable diluent such as, for example, alcohols (for example methanol or ethanol), ethers (for example diethyl ether or dioxane) or water or a mixture of these diluents (for example dioxane/water)
  • Suitable bases are inorganic or organic bases, in particular carbonates, such as, for example, sodium carbonate.
  • Pd(PPh 3 ) 4 PdCl 2 (PPh 3 ) 2
  • boronic acids or boronic esters of the formula (V) are commercially available, or they can be prepared by known methods. This is described, for example, in WO 1999/64428.
  • the products obtained after work-up can be purified in a customary manner by recrystallization, distillation under reduced pressure or column chromatography (cf also the Preparation Examples).
  • the active compounds according to the invention in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing the harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in the protection of stored products and of materials, and in the hygiene sector. They may be preferably employed as plant protection agents. They are active against normally sensitive and resistant species and against all or some stages of development.
  • the abovementioned pests include:
  • Anoplura for example, Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Triehodeetes spp.
  • Acarus siro Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus lat
  • Gastropoda From the class of the Gastropoda, for example, Anion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Succinea spp.
  • helminths from the class of the helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp, Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Lo
  • Hymenoptera From the order of the Hymenoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
  • Isopoda for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber.
  • Orthoptera for example, Acheta domesticus, Blatta orientalis, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca gregaria.
  • Siphonaptera for example, Ceratophyllus spp., Xenopsylla cheopis.
  • Symphyla for example, Scutigerella immaculata.
  • Thysanoptera From the order of the Thysanoptera, for example, Basothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp.
  • Thysanura for example, Lepisma saccharina.
  • the phytoparasitic nematodes include, for example, Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp., Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipenetrans, Xiphinema spp.
  • the compounds according to the invention can, at certain concentrations or application rates, also be used as herbicides, safeners, growth regulators or agents to improve plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including agents against viroids) or as agents against MLO (Mycoplasma-like organisms) and RLO (Rickettsia-like organisms). If appropriate, they can also be employed as intermediates or precursors for the synthesis of other active compounds.
  • the active compounds can be converted to the customary formulations, such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, granules for broadcasting, suspension-emulsion concentrates, natural materials impregnated with active compound, synthetic materials impregnated with active compound, fertilizers and microencapsulations in polymeric substances.
  • customary formulations such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, granules for broadcasting, suspension-emulsion concentrates, natural materials impregnated with active compound, synthetic materials impregnated with active compound, fertilizers and microencapsulations in polymeric substances.
  • formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surfactants, that is emulsifiers and/or dispersants and/or foam-formers.
  • extenders that is liquid solvents and/or solid carriers
  • surfactants that is emulsifiers and/or dispersants and/or foam-formers.
  • the formulations are prepared either in suitable plants or else before or during the application.
  • auxiliaries are substances which are suitable for imparting to the composition itself and/or to preparations derived therefrom (for example spray liquors, seed dressings) particular properties such as certain technical properties and/or also particular biological properties.
  • suitable auxiliaries are: extenders, solvents and carriers.
  • Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide).
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • the alcohols and polyols
  • suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethyl sulphoxide, and also water.
  • aromatics such as xylene, toluene or alkylnaphthalenes
  • chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride
  • aliphatic hydrocarbons such as cyclo
  • Suitable solid carriers are:
  • suitable solid carriers for granules are: for example, crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, and also synthetic granules of inorganic and organic meals, and granules of organic material such as paper, sawdust, coconut shells, maize cobs and tobacco stalks;
  • suitable emulsifiers and/or foam-formers are: for example, nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates and also protein hydroly
  • oligo- or polymers for example those derived from vinylic monomers, from acrylic acid, from EO and/or PO alone or in combination with, for example, (poly)alcohols or (poly)amines. It is also possible to employ lignin and its sulphonic acid derivatives, unmodified and modified celluloses, aromatic and/or aliphatic sulphonic acids and their adducts with formaldehyde.
  • Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations.
  • colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • organic dyestuffs such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs
  • trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • perfumes mineral or vegetable, optionally modified oils, waxes and nutrients (including trace nutrients), such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Stabilizers such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability may also be present.
  • the formulations generally comprise between 0.01 and 98% by weight of active compound, preferably between 0.5 and 90%.
  • the active compound according to the invention can be present in its commercially available formulations and in the use forms, prepared from these formulations, as a mixture with other active compounds, such as insecticides, attractants, sterilizing agents, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • active compounds such as insecticides, attractants, sterilizing agents, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • a mixture with other known active compounds, such as herbicides, fertilizers, growth regulators, safeners, semiochemicals, or else with agents for improving the plant properties, is also possible.
  • the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with synergistic agents.
  • Synergistic agents are compounds which increase the action of the active compounds, without it being necessary for the synergistic agent added to be active itself.
  • the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with inhibitors which reduce degradation of the active compound after use in the environment of the plant, on the surface of parts of plants or in plant tissues.
  • the active compound content of the use forms prepared from the commercially available formulations can vary within wide limits.
  • the active compound concentration of the use forms can be from 0.00000001 to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
  • Plants are to be understood as meaning in the present context all plants and plant populations such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
  • Crop plants can be plants which can be obtained by conventional plant breeding and optimization methods or by biotechnological and genetic engineering methods or by combinations of these methods, including the transgenic plants and including the plant cultivars protectable or not protectable by plant breeders' rights.
  • Plant parts are to be understood as meaning all parts and organs of plants above and below the ground, such as shoot, leaf, flower and root, examples which may be mentioned being leaves, needles, stalks, stems, flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes.
  • the plant parts also include harvested material, and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
  • Treatment according to the invention of the plants and plant parts with the active compounds is carried out directly or by allowing the compounds to act on the surroundings, habitat or storage space by the customary treatment methods, for example by immersion, spraying, evaporation, fogging, scattering, painting on, injection and, in the case of propagation material, in particular in the case of seeds, also by applying one or more coats.
  • the compounds according to the invention are particularly suitable for the treatment of seed.
  • most of the damage to crop plants which is caused by pests occurs as early as when the seed is infested during storage and after the seed is introduced into the soil, and during and immediately after germination of the plants.
  • This phase is particularly critical since the roots and shoots of the growing plants are particularly sensitive and even minor damage can lead to the death of the whole plant.
  • Protecting the seed and the germinating plant by the use of suitable compositions is therefore of particularly great interest.
  • the present invention therefore in particular also relates to a method for the protection of seed and germinating plants from attack by pests, by treating the seed with a composition according to the invention.
  • the invention likewise relates to the use of the compositions according to the invention for the treatment of seed for protecting the seed and the germinating plant from pests.
  • the invention relates to seed which has been treated with a composition according to the invention so as to afford protection from pests.
  • compositions according to the invention mean that treatment of the seed with these compositions not only protects the seed itself, but also the resulting plants after emergence, from pests. In this manner, the immediate treatment of the crop at the time of sowing or shortly thereafter can be dispensed with.
  • the compounds according to the invention can also be employed in particular in transgenic seed, the plants arising from this seed being capable of expressing a protein directed against pests.
  • certain pests can be controlled merely by the expression of the, for example, insecticidal protein, and, in addition, the seed can be protected from damage by the composition according to the invention.
  • compositions according to the invention are suitable for protecting seed of any plant variety as already mentioned above which is employed in agriculture, in the greenhouse, in forests or in horticulture.
  • this takes the form of seed of maize, peanut, canola, oilseed rape, poppy, soya beans, cotton, beet (for example sugar beet and fodder beet), rice, sorghum and millet, wheat, barley, oats, rye, sunflower, tobacco, potato or vegetables (e.g. tomatoes or brassicas).
  • the compositions according to the invention are likewise suitable for treating the seed of fruit plants and vegetables as already mentioned above.
  • the treatment of the seed of maize, soya beans, cotton, wheat and canola or oilseed rape is of particular importance.
  • transgenic seed is also of particular importance.
  • the heterologous genes in transgenic seed may be derived from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium .
  • the present invention is particularly suitable for the treatment of transgenic seed which comprises at least one heterologous gene originating from Bacillus sp. and whose gene product shows activity against the European corn borer and/or the corn root worm. It is particularly preferably a heterologous gene derived from Bacillus thuringiensis.
  • the active compounds according to the invention is applied to the seed either alone or in a suitable formulation.
  • the seed is treated in a state in which it is stable enough to avoid damage during treatment.
  • the seed may be treated at any point in time between harvest and sowing.
  • the seed usually used has been separated from the plant and freed from cobs, shells, stalks, coats, hairs or the flesh of the fruits.
  • the amount of the composition according to the invention applied to the seed and/or the amount of further additives is chosen in such a way that the germination of the seed is not adversely affected, or that the resulting plant is not damaged. This must be borne in mind in particular in the case of active compounds which can have phytotoxic effects at certain application rates.
  • plants and their parts it is possible to treat all plants and their parts according to the invention.
  • wild plant species and plant cultivars, or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and parts thereof, are treated.
  • transgenic plants and plant cultivars obtained by genetic engineering methods, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the terms “parts”, “parts of plants” and “plant parts” have been explained above.
  • plants of the plant cultivars which are in each case commercially available or in use are treated according to the invention.
  • Plant cultivars are to be understood as meaning plants having novel properties (“traits”) which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be cultivars, bio- or genotypes.
  • the treatment according to the invention may also result in superadditive (“synergistic”) effects.
  • superadditive for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the substances and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, higher quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
  • transgenic plants or plant cultivars which are preferably to be treated according to the invention include all plants which, by virtue of the genetic modification, received genetic material which imparted particularly advantageous, useful traits to these plants.
  • traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, higher quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products.
  • traits are a better defence of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and/or viruses, and also increased tolerance of the plants to certain herbicidally active compounds.
  • animal and microbial pests such as against insects, mites, phytopathogenic fungi, bacteria and/or viruses
  • traits are a better defence of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and/or viruses, and also increased tolerance of the plants to certain herbicidally active compounds.
  • (transgenic) plants which may be mentioned are the important crop plants, such as cereals (wheat, rice), maize, soya beans, potatoes, sugar beet, tomatoes, peas and other vegetable varieties, cotton, tobacco, oilseed rape and also fruit plants (with the fruits apples, pears, citrus fruits and grapes), and particular emphasis is given to maize, soya beans, potatoes, cotton, tobacco and oilseed rape.
  • Traits that are emphasized are in particular increased defence of the plants against insects, arachnids, nematodes and slugs and snails by virtue of toxins formed in the plants, in particular those formed in the plants by the genetic material from Bacillus thuringiensis (for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c, Cry2Ab, Cry3Bb and CryIF and also combinations thereof) (referred to hereinbelow as “Bt plants”).
  • Bacillus thuringiensis for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c, Cry2Ab, Cry3Bb and CryIF and also combinations thereof
  • Traits that are also particularly emphasized are the increased defence of the plants against fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins. Traits that are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulphonylureas, glyphosate or phosphinotricin (for example the “PAT” gene).
  • the genes which impart the desired traits in question can also be present in combination with one another in the transgenic plants.
  • Bt plants are maize varieties, cotton varieties, soya bean varieties and potato varieties which are sold under the trade names YIELD GARD® (for example maize, cotton, soya beans), KnockOut® (for example maize), StarLink® (for example maize), Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato).
  • YIELD GARD® for example maize, cotton, soya beans
  • KnockOut® for example maize
  • StarLink® for example maize
  • Bollgard® cotton
  • Nucotn® cotton
  • NewLeaf® potato
  • herbicide-tolerant plants examples include maize varieties, cotton varieties and soya bean varieties which are sold under the trade names Roundup Ready® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link® (tolerance to phosphinotricin, for example oilseed rape), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulphonylureas, for example maize).
  • Herbicide-resistant plants plants bred in a conventional manner for herbicide tolerance
  • Clearfield® for example maize.
  • the plants listed can be treated according to the invention in a particularly advantageous manner with the compounds of the formula (I).
  • the preferred ranges stated above for the active compounds also apply to the treatment of these plants. Particular emphasis is given to the treatment of plants with the compounds or mixtures specifically mentioned in the present text.
  • the active compounds according to the invention act not only against plant, hygiene and stored product pests, but also in the veterinary medicine sector against animal parasites (ecto- and endoparasites), such as hard ticks, soft ticks, mange mites, leaf mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, feather lice and fleas.
  • animal parasites ecto- and endoparasites
  • ecto- and endoparasites such as hard ticks, soft ticks, mange mites, leaf mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, feather lice and fleas.
  • parasites include:
  • Anoplurida for example, Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
  • Nematocerina and Brachycerina for example, Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Chrysomyia s
  • Siphonaptrida From the order of the Siphonaptrida, for example, Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
  • Actinedida Prostigmata
  • Acaridida Acaridida
  • Acarapis spp. Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
  • the active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which infest agricultural productive livestock, such as, for example, cattle, sheep, goats, horses, pigs, donkeys, camels, buffalo, rabbits, chickens, turkeys, ducks, geese and bees, other pets, such as, for example, dogs, cats, caged birds and aquarium fish, and also so-called test animals, such as, for example, hamsters, guinea pigs, rats and mice.
  • arthropods By controlling these arthropods, cases of death and reduction in productivity (for meat, milk, wool, hides, eggs, honey etc.) should be diminished, so that more economic and easier animal husbandry is possible by use of the active compounds according to the invention.
  • the active compounds according to the invention are used in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, potions, drenches, granules, pastes, boluses, the feed-through process and suppositories, by parenteral administration, such as, for example, by injection (intramuscular, subcutaneous, intravenous, intraperitoneal and the like), implants by nasal administration, by dermal use in the form, for example, of dipping or bathing, spraying, pouring on and spotting on, washing and powdering, and also with the aid of moulded articles containing the active compound, such as collars, ear marks, tail marks, limb bands, halters, marking devices and the like.
  • enteral administration in the form of, for example, tablets, capsules, potions, drenches, granules, pastes, boluses, the feed-through process and suppositories
  • parenteral administration such as,
  • the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, free-flowing compositions), which comprise the active compounds in an amount of 1 to 80% by weight, directly or after 100 to 10 000-fold dilution, or they can be used as a chemical bath.
  • the compounds according to the invention also have a strong insecticidal action against insects which destroy industrial materials.
  • insects may be mentioned as examples and as preferred—but without any limitation:
  • Hymenopterons such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur;
  • Termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus;
  • Bristletails such as Lepisma saccharina.
  • Industrial materials in the present connection are to be understood as meaning non-living materials, such as, preferably, plastics, adhesives, sizes, papers and cardboards, leather, wood and processed wood products and coating compositions.
  • the ready-to-use compositions may, if appropriate, comprise further insecticides and, if appropriate, one or more fungicides.
  • the compounds according to the invention can likewise be employed for protecting objects which come into contact with saltwater or brackish water, such as hulls, screens, nets, buildings, moorings and signalling systems, against fouling.
  • the compounds according to the invention may be employed as antifouling agents.
  • the active compounds are also suitable for controlling animal pests, in particular insects, arachnids and mites, which are found in enclosed spaces such as, for example, dwellings, factory halls, offices, vehicle cabins and the like. They can be employed alone or in combination with other active compounds and auxiliaries in domestic insecticide products for controlling these pests. They are active against sensitive and resistant species and against all developmental stages. These pests include:
  • Acarina for example, Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.
  • Opiliones From the order of the Opiliones, for example, Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
  • Saltatoria for example, Acheta domesticus.
  • Anthrenus spp. From the order of the Coleoptera, for example, Anthrenus spp., Attagenus spp., Dermestes spp., Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum.
  • Aedes aegypti Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria, Simulium spp., Stomoxys calcitrans, Tipula paludosa.
  • Lepidoptera From the order of the Lepidoptera, for example, Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.
  • Ctenocephalides canis Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.
  • Hymenoptera From the order of the Hymenoptera, for example, Camponotus herculeanus, Lasius faliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitam.
  • Pediculus humanus capitis for example, Pediculus humanus capitis, Pediculus humanus corporis, Pemphigus spp., Phylloera vastatrix, Phthirus pubis.
  • 6-Chloro-N-cyclopropylpyrimidine-4,5-diamine (cf. Journal of Combinatorial Chemistry (2003), 5(5), 653-659) (3.0 g, 16.2 mmol) was initially charged in a mixture of methylene chloride (12.20 ml) and pyridine (3.94 ml). The suspension was cooled to 0° C., and solid 2-ethylnicotinoyl chloride (1.2 eq) was added. The reaction mixture was allowed to warm to room temperature and stirred until the reaction had gone to completion. 10 ml of methylene chloride were then added, the suspension turning into a solution.
  • 6-(4-Chlorophenyl)-N-cyclopropylpyrimidine-4,5-diamine (1.00 g, 3.83 mmol) was initially charged in a mixture of DCM (3.20 ml) and pyridine (0.93 ml) and cooled to 0° C.
  • Solid 2-ethylnicotinoyl chloride (780 mg, 4.60 mmol) was added, and the reaction mixture was warmed to room temperature and stirred for another hour. After addition of semisaturated NaHCO 3 solution, the organic phase was separated off and concentrated under reduced pressure.
  • the compound from Example 6 (349 mg) was initially charged in a mixture of methylene chloride (3 ml) and pyridine (0.35 ml). The suspension was cooled to 0° C., and solid 2-ethylnicotinoyl chloride (1.2 eq) was added. The reaction mixture was allowed to warm to room temperature and stirred until the reaction had gone to completion. 10 ml of methylene chloride were then added, the suspension turning into a solution. After addition of semisaturated NaHCO 3 solution, the mixture was stirred and the organic phase was separated off and concentrated under reduced pressure.
  • R in column R 1 (cf., for example, Ex. Nos. 1-222, 1-229, 1-230, 1-250, 3-7 etc.) denotes the point of attachment to the remainder of the molecule.
  • Vessels containing horse meat treated with the active compound preparation of the desired concentration are populated with Lucilia cuprina larvae.
  • the activity in % is determined. 100% means that all larvae have been killed; 0% means that none of the larvae has been killed.
  • Vessels containing a sponge treated with the active compound preparation of the desired concentration are populated with adult Musca domestica.
  • the activity in % is determined. 100% means that all flies have been killed; 0% means that none of the flies has been killed.
  • active compound 10 mg of active compound are mixed with 0.5 ml of solvent, and the concentrate is diluted with water to the desired concentration.
  • the solution of active compound is injected into the abdomen ( Boophilus microplus ), the animals are trans-ferred into dishes and stored in a climatized room. Activity is assessed via oviposition of fertile eggs.
  • the activity in % is determined. 100% means that none of the ticks has laid any fertile eggs.
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • the activity in % is determined. 100% means that all aphids have been killed; 0% means that none of the aphids has been killed.
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of Chinese cabbage ( Brassica pekinensis ) are sprayed with an active compound preparation of the desired concentration and, after drying, populated with larvae of the mustard beetle (Phaedon cochleariae).
  • the activity in % is determined. 100% means that all beetle larvae have been killed; 0% means that none of the beetle larvae has been killed.
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of maize leaves ( Zea mays ) are sprayed with an active compound preparation of the desired concentration and, after drying, populated with caterpillars of the armyworm (Spodoptera frugiperda).
  • the activity in % is determined. 100% means that all caterpillars have been killed; 0% means that none of the caterpillars has been killed.
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of bean leaves Phaseolus vulgaris ) infested by all stages of the greenhouse red spider mite ( Tetranychus urticae ) are sprayed with an active compound preparation of the desired concentration.
  • the activity in % is determined. 100% means that all spider mites have been killed; 0% means that none of the spider mites has been killed.
  • active compound 10 mg are dissolved in 0.5 ml solvent, and the concentrate is diluted with solvent to the desired concentration.
  • Five adult engorged female ticks Boophilus microplus ) are injected with 1 n1 compound solution into the abdomen. Ticks are transferred into replica plates and incubated in a climate chamber for a period of time. Egg deposition of fertile eggs is monitored.
  • active compound 10 mg are dissolved in 0.5 ml solvent, and the concentrate is diluted with water to the desired concentration. Prior to the assay, a piece or kitchen sponge is soaked with a mixture of sugar and compound solution and placed into a container. 10 adults ( Musca domestica ) are placed into the container and closed with a perforated lid. After 2 days mortality in % is determined. 100% means that all the flies have been killed; 0% means that none of the flies have been killed.
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Chinese cabbage Brassica pekinesis
  • leaf-disks infected with all instars of the green peach aphid Myzus persicae
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Chinese cabbage ( Brassica pekinesis ) leaf-disks are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf disks are infested with mustard beetle larvae ( Phaedon cochleariae ).
  • a suitable preparation of the active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is dilutes with emulsifier-containing water to the desired concentration.
  • Maize (Zeaaria) leaf sections are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf sections are infested with fall armyworm larvae ( Spodoptera frugiperda ).
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • French beans Phaseolus vulgaris
  • the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • French beans Phaseolus vulgaris
  • Tetranychus urticae which are heavily infested with all stages of the two spotted spidermite ( Tetranychus urticae ) are sprayed with a preparation of the active ingredient at the desired concentration.
  • test solutions were prepared as follows:
  • test solution 1 part by weight of an active compound is mixed with the above-mentioned amount of solvent containing the above-mentioned amount of emulsifier, and the mixture is diluted with water to the desired concentration.
  • Leaves of sweet potato were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then placed in a petri dish having a diameter of 9 cm, and ten Spodoptera litura at third instar larvae were released therein. The petri dishes were placed in a temperature-controlled chamber at 25° C. After 2 days and 4 days more sweet potato leaves were added. After 7 days, the number of dead larvae was counted to calculate the insecticidal activity. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed. In the current test, the results of two petri dishes for each treatment were averaged.
  • Leaves of cucumber were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then put in a plastic cup containing sterilized black soil and five Aulacophora femoralis at second instar larvae were released in the cup. The cups were placed in a temperature-controlled chamber at 25° C. After 7 days, the number of dead larvae was counted, and thus the insecticidal activity was calculated. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed.

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Abstract

The present application relates to novel aminopyrimidinamides, to processes for their preparation and to their use for controlling animal pests, especially arthropods, in particular insects.

Description

  • The present application relates to novel aminopyrimidinamides, to processes for their preparation and to their use as pesticides and in particular as insecticides and/or parasiticides.
  • Modern crop protection agents have to satisfy many demands, for example with respect to efficacy, persistence and spectrum of their action and possible use. Questions of toxicity, the combinability with other active compounds or formulation auxiliaries play a role, as well as the question of the expense that the synthesis of an active compound requires. Furthermore, resistances may occur. For all these reasons, the search for novel crop protection agents cannot be considered as having been concluded, and there is a constant need for novel compounds having properties which, compared to the known compounds, are improved at least in respect of individual aspects.
  • WO 2002/067684 discloses certain pyridylpyrimidines as pesticides. However, they do not meet all demands in a satisfactory manner.
  • It was an object of the present invention to provide compounds which widen the spectrum of the pesticides under various aspects.
  • This object and further objects not explicitly mentioned which can be derived or deduced from the context discussed here are achieved by novel compounds of the formula (I)
  • Figure US20120071496A1-20120322-C00001
  • in which
    • R1 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, halocycloalkylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, hetheterocyclyl and heterocyclylalkyl,
    • R2 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
    • R3 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
    • R4 represents a radical from the group consisting of in each case optionally substituted phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl
    • R5 represents a radical from the group consisting of hydrogen, halogen, cyano and in each case optionally substituted alkyl, cycloalkyl, phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
    • R6 represents a radical from the group consisting of hydrogen, halogen, alkyl, haloalkyl, cyanoalkyl, alkoxyalkyl, alkylcarbonyl, haloalkylcarbonyl, cycloalkyl, halocycloalkyl, cycloalkylalkyl, alkylsulphonyl, alkenyl, alkynyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, alkoxycarbonylalkyl; optionally substituted phenyl, optionally substituted naphthyl, optionally substituted phenylalkyl, optionally substituted heterocyclylalkyl, optionally substituted heteroarylalkyl and optionally substituted phenylcarbonyl and
    • X represents oxygen or sulphur.
  • Furthermore, it has been found that compounds of the formula (I) can be prepared (Process 1) by reacting compounds of the formula (II)
  • Figure US20120071496A1-20120322-C00002
  • in which
    • R1, R2, R3, R5 and R6 have the meanings given above,
      with a compound of the formula (III)
    • R4CXHal (III)
      in which
    • X has the meaning given above and
    • Hal represents halogen, in particular chlorine,
      in the presence of a diluent and in the presence of a base.
  • Compounds of the formula (I) can also be prepared (Process 2) by reacting compounds of the formula (IV)
  • Figure US20120071496A1-20120322-C00003
  • in which
    • R1, R2, R3, R4 and R6 have the meanings given above and
    • LG represents chlorine, bromine, iodine or alkylsulphonyl,
      with boronic acids or boronic esters of the formula (V)

  • R5—B(ORa)2
  • in which
    • R5 has the meanings given above and
    • Ra represents hydrogen or alkyl (in particular C1-C4-alkyl),
      in the presence of a diluent, a palladium catalyst and a base (Suzuki reaction).
  • Finally, it has been found that the novel compounds of the formula (I) have pronounced biological properties and are suitable especially for controlling animal pests, in particular insects, arachnids and nematodes, encountered in agriculture, in forests, in the protection of stored products and materials and in the hygiene sector.
  • If appropriate, the compounds of the formula (I) may, depending on the nature of the substituents, be present as geometrical and/or as optically active isomers or corresponding isomer mixtures or in various tautomeric forms of varying compositions. The invention relates both to the pure isomers and to the isomer mixtures.
  • If appropriate, the compounds of the formula (I) may be present in various polymorphic forms or as mixtures of different polymorphic forms. The invention provides both the pure polymorphs and the polymorph mixtures, and both can be used according to the invention.
  • The formula (I) provides a general definition of the compounds according to the invention.
  • Preferred substituents or ranges of the radicals listed under the formulae mentioned above and below are illustrated below.
    • R1 preferably represents a radical from the group consisting of C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-haloalkyl, cyano-C1-C6-alkyl, C3-C8-cycloalkyl (in particular C3-C6-cycloalkyl), C3-C8-halocycloalkyl, C3-C8-cycloalkenyl, C3-C8-halocycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-haloalkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, alkyl, C1-C6-alkylsulphinyl-C1-C6-alkyl, C1-C6-alkylsulphonyl-C1-C6-alkyl, C1-C6-haloalkylsulphanyl-C1-C6-alkyl, C1-C6-haloalkylsulphinyl-C1-C6-alkyl, C1-C6-haloalkylsulphonyl-C1-C6-alkyl, C3-C8-cycloalkyl-C1-C6-alkyl, halogenated C3-C8-cycloalkyl-C1-C6-alkyl, phenyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-allylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH/=O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano and heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano.
    • R2 preferably represents a radical from the group consisting of hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-haloalkyl, cyano-C1-C6-alkyl, C3-C8-cycloalkyl (in particular C3-C6-cycloalkyl), C3-C8-halocycloalkyl, C3-C8-cycloalkenyl, C3-C8-halocycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-haloalkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, C1-C6-alkylsulphanyl-C1-C6-alkyl, C1-C6-alkylsulphinyl-C1-C6-alkyl, C1-C6-alkylsulphonyl-C1-C6-alkyl, C1-C6-haloalkylsulphanyl-C1-C6-alkyl, C1-C6-haloalkylsulphinyl-C1-C6-alkyl, C1-C6-haloalkylsulphonyl-C1-C6-alkyl, C3-C8-cycloalkyl-C1-C6-alkyl, phenyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH/=O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano and heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/—NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano.
    • R3 preferably represents a radical from the group consisting of hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, halo-C1-C6-alkyl, cyano-C1-C6-alkyl, C3-C8-cycloalkyl, halo-C3-C8-cycloalkyl, C3-C8-cycloalkenyl, halo-C3-C8-cycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, C1-C6-alkylsulphanyl-C1-C6-alkyl, C1-C6-alkylsulphinyl-C1-C6-alkyl, C1-C6-alkylsulphonyl-C1-C6-alkyl, C3-C8-cycloalkyl-C1-C6-alkyl, phenyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano and heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkyl sulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano.
    • R4 preferably represents a radical from the group consisting of phenyl, 2-pyridyl, 3-pyridyl and pyrazolyl which are in each case optionally mono- or polysubstituted by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-cycloalkyl-C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy, COOH, nitro, amino, cyano, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, C1-C6-alkylaminocarbonyl, C3-C6-cycloalkylaminocarbonyl, phenyl (which for its part may be substituted by halogen), and hetaryl-C1-C6-alkyl (in particular pyrazolyl-C1-C6-alkyl (which for its part may be substituted by halogen, C1-C6-alkyl and C1-C6-haloalkyl)).
    • R5 preferably represents a radical from the group consisting of hydrogen, halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl and also phenyl, 2-pyridyl or 3-pyridyl which are in each case optionally mono- or polysubstituted by identical or different radicals from the group consisting of halogen, amino, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy, nitro, cyano, C1-C6-alkylcarbonyl, C1-C6-alkylcarbonylamino, C3-C6-cycloalkylcarbonylamino, C1-C6-alkylaminocarbonyl, C3-C6-cycloalkylaminocarbonyl C1-C6-alkoxycarbonyl, aminocarbonyl, C1-C6-alkoxyimino-C1-C6-alkyl, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-allylsulphonyl, C1-C6-alkylsulphonyloxy, C1-C6-alkylsulphonylamino, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, tri-C1-C6-alkylsilyl, S(O)(═N—CN), S(O)(═N)R (in which R represents C1-C6-alkyl or C1-C6-haloalkyl), phenyl, phenyl-C1-C6-alkyl, phenyl-C1-C6-alkyloxy, phenyloxy, pyrazolyl (where the phenyl groups or the pyrazolyl ring for their part may be substituted by halogen, C1-C6-alkyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, nitro, cyano, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-alkylsulphonyloxy, C1-C6-alkyl sulphonylam ino, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-hal oalkylsulphonyl, S(O)(═N—CN), S(O)(═N)R (in which R represents C1-C6-alkyl or C1-C6-haloalkyl)), hetaryloxy-C1-C6-alkyl, hetaryloxy and hetaryl-C1-C6-alkyl, (where the hetaryl radical is in each case selected from the group consisting of pyrrolyl, imidazolyl, pyrazolyl, triazolyl, pyridyl, pyrimidinyl and tetrazolyl and may for its part be substituted by halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl) and where two adjacent substituents together may also represent —OCH2O—, —OCF2O— or —OCH2CH2O— (cf. Ex. No. 1-12).
    • R6 preferably represents a radical from the group consisting of hydrogen, halogen, C1-C6-alkyl, C1-C6-haloalkyl, cyano-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl, C1-C6-haloalkylcarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C3-C8-cycloalkyl-C1-C6-alkyl, C1-C6-alkylsulphanyl, C1-C6-alkylsulphonyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxycarbonyl, C2-C6-alkenyloxycarbonyl, C2-C6-alkynyloxycarbonyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl; phenyl, phenyl-C1-C6-alkyl which are in each case optionally mono- or polysubstituted at the phenyl ring by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; or phenylcarbonyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano.
    • X preferably represents oxygen or sulphur.
    • R1 particularly preferably represents a radical from the group consisting of C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-haloalkyl, C3-C8-cycloalkyl (in particular C3-C6-cycloalkyl), C3-C8-halocycloalkyl, C3-C8-cycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylsulphanyl-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl. C1-C6-alkoxycarbonyl-C1-C6-alkyl, C3-C6-cycloalkyl-C1-C6-alkyl, halogenated C3-C6-cycloalkyl-C1-C6-alkyl, phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano.
    • R2 particularly preferably represents a radical from the group consisting of hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-haloalkyl, C3-C8-cycloalkyl (in particular C3-C6-cycloalkyl), C3-C8-halocycloalkyl, C3-C8-cycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro
    • R3 particularly preferably represents a radical from the group consisting of hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-haloalkyl, C3-C8-cycloalkyl (in particular C3-C6-cycloalkyl), C3-C8-halocycloalkyl, C3-C8-cycloalkenyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, phenyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heteroaryl which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heteroaryl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heteroaromatic moiety by identical or different substituents from the group consisting of —OH, —SH, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano; heterocyclyl-C1-C6-alkyl which is optionally mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of —OH/═O, —SH/═S, —NH2, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, nitro or cyano.
    • R4 particularly preferably represents 3-pyridyl or pyrazolyl which are in each case optionally mono- or polysubstituted by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-cycloalkyl-C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy, COOH, nitro, amino, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, C1-C6-alkylaminocarbonyl and C3-C6-cycloalkylaminocarbonyl.
    • R4 furthermore also particularly preferably represents phenyl which is optionally substituted by halogen, cyano, C1-C6-alkyl and C1-C6-haloalkyl.
    • R4 furthermore also particularly preferably represents pyrazolyl which is optionally substituted by halogen or C1-C6-alkyl, phenyl (which for its part may be substituted by halogen) or by pyrazolylmethyl (which for its part may be substituted by C1-C6-haloalkyl).
    • R5 particularly preferably represents phenyl, 2-pyridyl or 3-pyridyl (in particular phenyl) which are in each case optionally mono- or polysubstituted by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy, nitro, amino, cyano, mono-C1-C6-alkylamino, di-C1-C6-alkylamino, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, hetaryloxy-C1-C6-alkyl, hetaryloxy and hetaryl-C1-C6-alkyl, where the hetaryl radical is selected from the group consisting of pyrrolyl, imidazolyl, pyrazolyl, triazolyl, pyridyl, pyrimidinyl and tetrazolyl and for its part may be substituted by substituents from the group consisting of halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl and C3-C8-halocycloalkyl.
    • R5 also particularly preferably represents hydrogen, halogen, C1-C4-alkyl and C3-C6-cycloalkyl.
    • R6 particularly preferably represents a radical from the group consisting of hydrogen, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylcarbonyl, C1-C6-haloalkylcarbonyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-C1-C6-alkyl, C1-C6-alkylsulphanyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxycarbonyl, C2-C6-alkenyloxycarbonyl, C2-C6-alkynyloxycarbonyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, phenyl, phenyl-C1-C6-alkyl which are in each case optionally mono- or polysubstituted at the phenyl ring by identical or different radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; heterocyclyl-C1-C6-alkyl which may optionally be mono- or polysubstituted at the heterocycle by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano; and phenylcarbonyl which is optionally mono- or polysubstituted at the phenyl ring by identical or different substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, nitro or cyano.
    • X particularly preferably represents oxygen or sulphur, in particular oxygen.
    • R1 very particularly preferably represents a radical from the group consisting of C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkylsulphanyl-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl and C3-C6-cycloalkyl-C1-C6-alkyl and halogenated C3-C6-cycloalkyl-C1-C6-alkyl, in particular cyclopropyl.
    • R2 very particularly preferably represents hydrogen,
    • R3 very particularly preferably represents hydrogen,
    • R4 very particularly preferably represents 3-pyridyl which is mono- or polysubstituted by radicals from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-cycloalkyl-C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylaminocarbonyl and C3-C6-cycloalkylaminocarbonyl.
    • R4 furthermore very particularly preferably represents phenyl which is optionally substituted by halogen, cyano, C1-C6-alkyl and C1-C6-haloalkyl.
    • R4 furthermore very particularly preferably represents pyrazolyl (preferably 3-pyrazolyl) which may be substituted by halogen (preferably F, Cl, Br) and C1-C6-alkyl (preferably methyl, ethyl and propyl), phenyl (which for its part may be substituted by halogen) or by pyrazolylmethyl (which for its part may be substituted by C1-C6-haloalkyl, in particular fluorinated C1-C6-alkyl).
    • R5 very particularly preferably represents a radical from the group consisting of phenyl, 2-pyridyl and 3-pyridyl (in particular phenyl), each of which is mono- or polysubstituted by at least one radical from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, nitro, cyano, C1-C6-alkylsulphanyl, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-haloalkylsulphanyl, C1-C6-haloalkylsulphinyl, C1-C6-haloalkylsulphonyl, hetaryloxy-C1-C6-alkyl, hetaryloxy and hetaryl-C1-C6-alkyl, where the hetaryl radical is selected from the group consisting of pyrrolyl, imidazolyl, pyrazolyl, triazolyl, pyridyl, pyrimidinyl and tetrazolyl and may for its turn be substituted by substituents from the group consisting of halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl and C3-C8-halocycloalkyl.
    • R5 also very particularly preferably represents a radical from the group consisting of hydrogen, halogen, C1-C4-alkyl and C3-C6-cycloalkyl.
    • R6 very particularly preferably represents a radical from the group consisting of hydrogen, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C1-C6alkylsulphanyl and phenyl which may be substituted by halogen.
    • X very particularly preferably represents oxygen.
    • R1 most preferably represents a radical from the group consisting of CH3, CH2CH3, CH(CH3)2, cyclopropyl, halocyclopropyl, C(CH3)3, CH(CH3)CH2SCH3, CH2CH2CH3, CH(CH3)CH2CH3, CH2CF3, CHCH3CF3, CH(CH3)cyclopropyl and with particular emphasis cyclopropyl,
    • R2 most preferably represents hydrogen.
    • R3 most preferably represents hydrogen.
    • R4 most preferably represents 3-pyridyl which is substituted in the 2-position by a substituent from the group consisting of F, Cl, Br, methyl, ethyl, CF3, CH2CF3, CHFCH3, CHFCF3, cyclopropyl and cyclopropylmethyl.
    • R4 furthermore most preferably represents phenyl which may be substituted by F, Cl, CN, CH3, C2H5, CF3 and C2F5.
    • R4 furthermore most preferably represents pyrazolyl (preferably 3-pyrazolyl) which may be substituted by F, Cl, methyl, ethyl or by pyrazolylmethyl which for its part may be substituted by C1-C6-haloalkyl, in particular by CF3.
    • R5 most preferably represents phenyl which is mono- or polysubstituted by a radical from the group consisting of CH3, F, Cl, CF3, CF(CF3)2, OCH3, OCF3, NO2, CN, SCF3, S(O)CF3 and S(O)2CF3 and CH2-Q.
    • Q represents a radical from the group consisting of
  • Figure US20120071496A1-20120322-C00004
  • where the arrow indicates the point of attachment to the CH2 group.
    • R6 most preferably represents hydrogen.
  • In the preferred definitions, unless indicated otherwise,
  • halogen (also in radicals such as, for example, haloalkyl) is selected from the group consisting of fluorine, chlorine, bromine and iodine, preferably from the group consisting of fluorine, chlorine and bromine,
    heteroaryl or hetaryl (also as part of a larger moiety such as, for example, heteroarylalkyl) is selected from the group consisting of furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, tetrazolyl, benzofuryl, benzisofuryl, benzothienyl, benzisothienyl, indolyl, isoindolyl, indazolyl, benzothiazolyl, benzisothiazolyl, benzoxazolyl, benzisoxazolyl, benzimidazolyl, 2,1,3-benzoxadiazole, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, benzotriazinyl, purinyl, pteridinyl and indolizinyl,
    heterocyclyl (also as part of a larger moiety such as, for example, heterocyclylalkyl) is selected from the group consisting of 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-pyrazolidinyl, pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,4-dihydrofur-2-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,4-dihydrothien-2-yl, 2-pyrrolin-2-yl, 2-pyrrolin-3-yl, 3-pyrrolin-2-yl, 2-isoxazolin-3-yl, 3-isoxazolin-3-yl, 4-isoxazolin-3-yl, 2-isoxazolin-4-yl, 3-isoxazolin-4-yl, 4-isoxazolin-4-yl, 2-isoxazolin-5-yl, 3-isoxazolin-5-yl, 4-isoxazolin-5-yl, 2-isothiazolin-3-yl, 3-isothiazolin-3-yl, 4-isothiazolin-3-yl, 2-isothiazolin-4-yl, 3-isothiazolin-4-yl, 4-isothiazolin-4-yl, 2-isothiazolin-5-yl, 3-isothiazolin-5-yl, 4-isothiazolin-5-yl, 2,3-dihydropyrazol-1-yl, 2,3-dihydropyrazol-2-yl, 2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl, 2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl, 3,4-dihydropyrazol-3-yl, 3,4-dihydropyrazol-4-yl, 3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1-yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl, 4,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 1,3-dioxan-5-yl, 2-tetrahydropyranyl, 4-tetrahydropyranyl, 2-tetrahydrothienyl, 3-hexahydropyridazinyl, 4-hexahydropyridazinyl, 2-hexahydropyrimidinyl, 4-hexahydropyrimidinyl, 5-hexahydropyrimidinyl, 2-piperazinyl, 1,3,5-hexahydrotriazin-2-yl and 1,2,4-hexahydrotriazin-3-yl.
  • In the particularly preferred definitions, unless indicated otherwise,
  • halogen is selected from the group consisting of fluorine, chlorine, bromine and iodine, preferably from the group consisting of fluorine, chlorine and bromine,
    heteroaryl or hetaryl (also as part of a larger moiety such as, for example, hetarylalkyl) is selected from the group consisting of pyrimidyl, oxadiazolyl, oxazolyl, pyrazinyl, imidazolyl, thiazolyl and furanyl, pyrrolyl, pyrazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, tetrazolyl,
    heterocyclyl (also as part of a larger moiety such as, for example, heterocyclylalkyl) is selected from the group consisting of 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,4-dihydrofur-2-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,4-dihydrothien-2-yl, 2-pyrrolin-2-yl, 2-pyrrolin-3-yl, 3-pyrrolin-2-yl, 3-pyrrolin-3-yl, 2-isoxazolin-3-yl, 3-isoxazolin-3-yl, 4-isoxazolin-3-yl, 2-isoxazolin-4-yl, 3-isoxazolin-4-yl, 4-isoxazolin-4-yl, 2-isoxazolin-5-yl, 3-isoxazolin-5-yl, 4-isoxazolin-5-yl, 2-isothiazolin-3-yl, 3-isothiazolin-3-yl, 4-isothiazolin-3-yl, 2-isothiazolin-4-yl, 3-isothiazolin-4-yl, 4-isothiazolin-4-yl, 2-isothiazolin-5-yl, 3-isothiazolin-5-yl, 4-isothiazolin-5-yl, 2,3-dihydropyrazol-1-yl, 2,3-dihydropyrazol-2-yl, 2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl, 2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl, 3,4-dihydropyrazol-3-yl, 3,4-dihydropyrazol-4-yl, 3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1-yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl, 4,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 1,3-dioxan-5-yl, 2-tetrahydropyranyl, 4-tetrahydropyranyl, 2-tetrahydrothienyl, 3-hexahydropyridazinyl, 4-hexahydropyridazinyl, 2-hexahydropyrimidinyl, 4-hexahydropyrimidinyl, 5-hexahydropyrimidinyl, 2-piperazinyl, 1,3,5-hexahydrotriazin-2-yl and 1,2,4-hexahydrotriazin-3-yl.
  • Halogen-substituted radicals, for example haloalkyl, are mono- or polysubstituted up to the maximum possible number of substituents. In the case of polyhalogenation, the halogen atoms can be identical or different. Here, halogen represents fluorine, chlorine, bromine and iodine, in particular fluorine, chlorine and bromine,
  • The general or preferred radical definitions or illustrations given above apply both to the end products and, correspondingly, to starting materials and intermediates. These radical definitions can be combined with one another as desired, i.e. including combinations between the given preferred ranges.
  • Preference according to the invention is given to the compounds of the formula (I) which contain a combination of the meanings listed above as being preferred.
  • Particular preference according to the invention is given to the compounds of the formula (I) which contain a combination of the meanings listed above as being particularly preferred.
  • Very particular preference according to the invention is given to the compounds of the formula (I) which contain a combination of the meanings listed above as being very particularly preferred.
  • Most preference according to the invention is given to the compounds of the formula (I) which contain a combination of the meanings listed above as being most preferred.
  • In a preferred group of compounds of the formula (I), R′ represents cyclopropyl.
  • In a further preferred group of compounds of the formula (I), R7 represents ethyl.
  • In a further preferred group of compounds of the formula (I), R7 represents CH2CF3.
  • In a further preferred group of compounds of the formula (I), R5 represents optionally substituted phenyl.
  • In a further preferred group of compounds of the formula (I), R5 represents optionally substituted 3-pyridyl.
  • If, in the Process 1 according to the invention for preparing the novel compounds of the formula (I), the compound of the formula (II) used is, for example, 6-(4-chlorophenyl)-N-cyclopropyl-pyrimidine-4,5-diamine and the compound of the formula (III) used is 2-ethylnicotinoyl chloride, Process 1 can be represented by Reaction Scheme I below:
  • Figure US20120071496A1-20120322-C00005
  • This reaction is generally carried out by reacting compounds of the formula (II) with compounds of the formula (III) in the presence of a basic auxiliary in a diluent at a temperature of from −40° C. to 120° C.
  • Suitable basic auxiliaries are amines, for example trialkylamines or pyridines. Pyridine may be mentioned by way of example.
  • In general, it is advantageous to react the compounds of the formula (II) with compounds of the formula (III) in a diluent. If appropriate, it may also be possible to employ mixtures of diluents for this purpose. Diluents are advantageously employed in such an amount that the reaction mixture remains readily stirrable during the entire process. Suitable diluents for carrying out the Process 1 according to the invention are organic solvents which are inert under the reaction conditions.
  • Examples which may be mentioned are: halogenated hydrocarbons, in particular chlorinated hydrocarbons, such as tetrachloroethylene, tetrachloroethane, dichloropropane, methylene chloride (DCM), dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichloroethylene, pentachloroethane, difluorobenzene, 1,2-dichloroethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene; ethers, such as ethyl propyl ether, methyl tert-butyl ether, n-butyl ether, anisole, phenetole, cyclohexyl methyl ether, dimethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, di-n-butyl ether, diisobutyl ether, diisoamyl ether, ethylene glycol dimethyl ether, tetrahydrofuran, dioxane, dichlorodiethyl ether and polyethers of ethylene oxide and/or propylene oxide.
  • After the reaction has ended, the entire reaction mixture is concentrated. The products obtained after work-up can be purified in a customary manner by recrystallization, distillation under reduced pressure or column chromatography (cf. also the Preparation Examples).
  • Some of the compounds of the formula (II) can be obtained commercially or by methods known from the literature (cf. Journal of Combinatorial Chemistry (2003), 5(5), 653-659, and also the Preparation Examples).
  • The formula (III) describes the compounds furthermore to be used as starting materials for carrying out Process 1 according to the invention.
  • In formula (III), R4 has the meanings already mentioned in connection with the description of the compounds of the formula (I) according to the invention.
  • Some of the compounds of the formula (III) are known and can be obtained commercially or by methods known from the literature (cf. Chemical Communications (2008), 4207-4209, and Methods of Organic Synthesis (2002) Volume E22a, Ed. Murray Goodman, JP401316361A and also Mendeleev Communications (2006) (3), 161-163).
  • If, in Process 2 according to the invention for preparing the compounds of the formula (I), the compound of the formula (IV) used is, for example, N-(4-chloro-6-cyclopropylaminopyrimidin-5-yl)-2-ethylnicotinamide and the compound of the formula (V) is 2,4-dichlorophenylboronic acid, the process can be represented by Reaction Scheme II below;
  • Figure US20120071496A1-20120322-C00006
  • The compound of the formula (IV) is reacted in a suitable diluent, such as, for example, alcohols (for example methanol or ethanol), ethers (for example diethyl ether or dioxane) or water or a mixture of these diluents (for example dioxane/water), if appropriate in the presence of a base and in the presence of suitable palladium catalysts and bases in a temperature range of from −20° C. to 120° C. in suitable solvents (Suzuki reaction).
  • Suitable bases are inorganic or organic bases, in particular carbonates, such as, for example, sodium carbonate.
  • A large number of palladium catalysts can be employed. Preference is given to using a catalyst from the group consisting of PdCl2(dppf) [dppf=1,1′-bis(diphenylphosphino)ferrocene], Pd(PPh3)4, PdCl2(PPh3)2, PdCl2(CH3CN)2, Pd2(dba)3 [dba=dibenzylideneacetone] or Pd(OAc)2, particularly preferably Pd(PPh3)4.
  • Some of the compounds of the formula (IV) are known and can be prepared by known methods described, for example, in Tetrahedron Letters, 49(13), 2143-2145; 2008.
  • Some of the boronic acids or boronic esters of the formula (V) are commercially available, or they can be prepared by known methods. This is described, for example, in WO 1999/64428.
  • After the reaction has ended, the entire reaction mixture is concentrated. The products obtained after work-up can be purified in a customary manner by recrystallization, distillation under reduced pressure or column chromatography (cf also the Preparation Examples).
  • The active compounds according to the invention, in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing the harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in the protection of stored products and of materials, and in the hygiene sector. They may be preferably employed as plant protection agents. They are active against normally sensitive and resistant species and against all or some stages of development. The abovementioned pests include:
  • From the order of the Anoplura (Phthiraptera), for example, Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Triehodeetes spp.
  • From the class of the Arachnida, for example, Acarus siro, Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vasates lycopersici.
  • From the class of the Bivalva, for example, Dreissena spp.
  • From the order of the Chilopoda, for example, Geophilus spp., Scutigera spp.
  • From the order of the Coleoptera, for example, Acanthoscelides obtectus, Adoretus spp., Agelastica alni, Agriotes spp., Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Anthonomus spp., Anthrenus spp., Apogonia spp., Atomaria spp., Attagenus spp., Bruchidius obtectus, Bruchus spp., Ceuthor Lynchus spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meligethes aeneus, Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Otiorrhynchus sulcatus, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Popillia japonica, Premnotrypes spp., Psylliodes chrysocephala, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Sitophilus spp., Sphenophorus spp., Sternechus spp., Symphyletes spp., Tenebrio molitor, Tribolium spp., Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp.
  • From the order of the Collembola, for example, Onychiurus armatus.
  • From the order of the Dermaptera, for example, Forficula auricularia,
  • From the order of the Diplopoda, for example, Blaniulus guttulatus.
  • From the order of the Diptera, for example, Aedes spp., Anopheles spp., Bibio hortulanus, Calliphora erythrocephala, Ceratitis capitata, Chrysomyia spp., Cochliomyia spp., Cordylobia anthropophaga, Culex spp., Cuterebra spp., Dacus oleae, Dermatobia hominis, Drosophila spp., Fannia spp., Gastrophilus spp., Hylemyia spp., Hyppobosca spp., Hypoderma spp., Liriomyza spp., Lucilia spp., Musca spp., Nezara spp., Oestrus spp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Stomoxys spp., Tabanus spp., Tannia spp., Tipula paludosa, Wohlfahrtia spp.
  • From the class of the Gastropoda, for example, Anion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Succinea spp.
  • From the class of the helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp, Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp, Strongyloides fuelleborni, Strongyloides stercoralis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti.
  • It is furthermore possible to control Protozoa, such as Eimeria.
  • From the order of the Heteroptera, for example, Anasa tristis, Antestiopsis spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., Creontiades dilutus, Dasynus piperic, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., Eurygaster spp., Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatus, Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.
  • From the order of the Homoptera, for example, Acyrthosipon spp., Aeneolamia spp., Agonoscena spp., Aleurodes spp., Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anuraphis cardui, Aonidiella spp., Aphanostigma pini, Aphis spp., Arboridia apicalis, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacorthum solani, Bemisia spp., Brachycaudus helichrysii, Brachycolus spp., Brevicoryne brassicae, Calligypona marginata, Carneocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halli, Coccus spp., Cryptomyzus ribis, Dalbulus spp., Dialeurodes spp., Diaphorina spp., Diaspis spp., Doralis spp., Diosicha spp., Dysaphis spp., Dysmicoccus spp., Empoasca spp., Eriosoma spp., Erythroneura spp., Euscelis bilobatus, Geococcus coffeae, Homalodisca coagulata, Hyalopterus arundinis, Icerya spp., Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Lipaphis erysimi, Macrosiphum spp., Mahanarva fimbriolata, Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., Nasonovia ribisnigri, Nephotettix spp., Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Parabemisia myricae, Paratrioza spp., Parlatoria spp., Pemphigus spp., Peregrinus maidis, Phenacoccus spp., Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Pinnaspis aspidistrae, Planococcus spp., Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Psylla spp., Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., Saissetia spp., Scaphoides titanus, Schizaphis graminum, Selenaspidus articulatus, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Tenalaphara malayensis, Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes vaporariorum, Trioza spp., Typhlocyba spp., Unaspis spp., Viteus vitifolii.
  • From the order of the Hymenoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
  • From the order of the Isopoda, for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber.
  • From the order of the Isoptera, for example, Reticulitermes spp., Odontotermes spp.
  • From the order of the Lepidoptera, for example, Acronicta major, Aedia leucomelas, Agrotis spp., Alabama argillacea, Anticarsia spp., Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius, Cacoecia podana, Capua reticulana, Carpocapsa pomonella, Chematobia brumata, Chilo spp., Choristoneura fumiferana, Clysia ambiguella, Cnaphalocerus spp., Earias insulana, Ephestia kuehniella, Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Helicoverpa spp., Heliothis spp., Hofmannophila pseudospretella, Homona magnanima, Hyponomeuta padella, Laphygma spp., Lithocolletis blancardella, Lithophane antennata, Loxagrotis albicosta, Lymantria spp., Malacosoma neustria, Mamestra brassicae, Mocis repanda, Mythimna separata, Oria spp., Oulema oryzae, Panolis flammea, Pectinophora gossypiella, Phyllocnistis citrella, Pieris spp., Plutella xylostella, Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Spodoptera spp., Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortrix viridana, Trichoplusia spp.
  • From the order of the Orthoptera, for example, Acheta domesticus, Blatta orientalis, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca gregaria.
  • From the order of the Siphonaptera, for example, Ceratophyllus spp., Xenopsylla cheopis.
  • From the order of the Symphyla, for example, Scutigerella immaculata.
  • From the order of the Thysanoptera, for example, Baliothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp.
  • From the order of the Thysanura, for example, Lepisma saccharina.
  • The phytoparasitic nematodes include, for example, Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp., Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipenetrans, Xiphinema spp.
  • If appropriate, the compounds according to the invention can, at certain concentrations or application rates, also be used as herbicides, safeners, growth regulators or agents to improve plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including agents against viroids) or as agents against MLO (Mycoplasma-like organisms) and RLO (Rickettsia-like organisms). If appropriate, they can also be employed as intermediates or precursors for the synthesis of other active compounds.
  • The active compounds can be converted to the customary formulations, such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, granules for broadcasting, suspension-emulsion concentrates, natural materials impregnated with active compound, synthetic materials impregnated with active compound, fertilizers and microencapsulations in polymeric substances.
  • These formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surfactants, that is emulsifiers and/or dispersants and/or foam-formers. The formulations are prepared either in suitable plants or else before or during the application.
  • Suitable for use as auxiliaries are substances which are suitable for imparting to the composition itself and/or to preparations derived therefrom (for example spray liquors, seed dressings) particular properties such as certain technical properties and/or also particular biological properties. Typical suitable auxiliaries are: extenders, solvents and carriers.
  • Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide).
  • If the extender used is water, it is also possible to employ, for example, organic solvents as auxiliary solvents. Essentially, suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethyl sulphoxide, and also water.
  • Suitable solid carriers are:
  • for example, ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and silicates; suitable solid carriers for granules are: for example, crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, and also synthetic granules of inorganic and organic meals, and granules of organic material such as paper, sawdust, coconut shells, maize cobs and tobacco stalks; suitable emulsifiers and/or foam-formers are: for example, nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates and also protein hydrolysates; suitable dispersants are nonionic and/or ionic substances, for example from the classes of the alcohol-POE- and/or -POP-ethers, acid and/or POP-POE esters, alkyl aryl and/or POP-POE ethers, fat- and/or POP-POE adducts, POE- and/or POP-polyol derivatives, POE- and/or POP-sorbitan- or -sugar adducts, alkyl or aryl sulphates, alkyl- or aryl sulphonates and alkyl or aryl phosphates or the corresponding PO-ether adducts. Furthermore, suitable oligo- or polymers, for example those derived from vinylic monomers, from acrylic acid, from EO and/or PO alone or in combination with, for example, (poly)alcohols or (poly)amines. It is also possible to employ lignin and its sulphonic acid derivatives, unmodified and modified celluloses, aromatic and/or aliphatic sulphonic acids and their adducts with formaldehyde.
  • Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations.
  • It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Other possible additives are perfumes, mineral or vegetable, optionally modified oils, waxes and nutrients (including trace nutrients), such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Stabilizers, such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability may also be present.
  • The formulations generally comprise between 0.01 and 98% by weight of active compound, preferably between 0.5 and 90%.
  • The active compound according to the invention can be present in its commercially available formulations and in the use forms, prepared from these formulations, as a mixture with other active compounds, such as insecticides, attractants, sterilizing agents, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • A mixture with other known active compounds, such as herbicides, fertilizers, growth regulators, safeners, semiochemicals, or else with agents for improving the plant properties, is also possible.
  • When used as insecticides, the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with synergistic agents. Synergistic agents are compounds which increase the action of the active compounds, without it being necessary for the synergistic agent added to be active itself.
  • When used as insecticides, the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with inhibitors which reduce degradation of the active compound after use in the environment of the plant, on the surface of parts of plants or in plant tissues.
  • The active compound content of the use forms prepared from the commercially available formulations can vary within wide limits. The active compound concentration of the use forms can be from 0.00000001 to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
  • The compounds are employed in a customary manner appropriate for the use forms.
  • All plants and plant parts can be treated in accordance with the invention. Plants are to be understood as meaning in the present context all plants and plant populations such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional plant breeding and optimization methods or by biotechnological and genetic engineering methods or by combinations of these methods, including the transgenic plants and including the plant cultivars protectable or not protectable by plant breeders' rights. Plant parts are to be understood as meaning all parts and organs of plants above and below the ground, such as shoot, leaf, flower and root, examples which may be mentioned being leaves, needles, stalks, stems, flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes. The plant parts also include harvested material, and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
  • Treatment according to the invention of the plants and plant parts with the active compounds is carried out directly or by allowing the compounds to act on the surroundings, habitat or storage space by the customary treatment methods, for example by immersion, spraying, evaporation, fogging, scattering, painting on, injection and, in the case of propagation material, in particular in the case of seeds, also by applying one or more coats.
  • The compounds according to the invention are particularly suitable for the treatment of seed. Thus, most of the damage to crop plants which is caused by pests occurs as early as when the seed is infested during storage and after the seed is introduced into the soil, and during and immediately after germination of the plants. This phase is particularly critical since the roots and shoots of the growing plants are particularly sensitive and even minor damage can lead to the death of the whole plant. Protecting the seed and the germinating plant by the use of suitable compositions is therefore of particularly great interest.
  • The control of pests by treating the seed of plants has been known for a long time and is the subject of continuous improvements. However, the treatment of seed entails a series of problems which cannot always be solved in a satisfactory manner. Thus, it is desirable to develop methods for protecting the seed and the germinating plant which dispense with the additional application of crop protection products after planting or after emergence of the plants. It is furthermore desirable to optimize the amount of active compound employed in such a way as to provide optimum protection for the seed and the germinating plant from attack by pests, but without damaging the plant itself by the active compound employed. In particular, methods for the treatment of seed should also take into consideration the intrinsic insecticidal properties of transgenic plants in order to achieve optimum protection of the seed and the germinating plant with a minimum of crop protection products being employed.
  • The present invention therefore in particular also relates to a method for the protection of seed and germinating plants from attack by pests, by treating the seed with a composition according to the invention. The invention likewise relates to the use of the compositions according to the invention for the treatment of seed for protecting the seed and the germinating plant from pests. Furthermore, the invention relates to seed which has been treated with a composition according to the invention so as to afford protection from pests.
  • One of the advantages of the present invention is that the particular systemic properties of the compositions according to the invention mean that treatment of the seed with these compositions not only protects the seed itself, but also the resulting plants after emergence, from pests. In this manner, the immediate treatment of the crop at the time of sowing or shortly thereafter can be dispensed with.
  • Furthermore, it must be considered as advantageous that the compounds according to the invention can also be employed in particular in transgenic seed, the plants arising from this seed being capable of expressing a protein directed against pests. By treating such seed with the compositions according to the invention, certain pests can be controlled merely by the expression of the, for example, insecticidal protein, and, in addition, the seed can be protected from damage by the composition according to the invention.
  • The compositions according to the invention are suitable for protecting seed of any plant variety as already mentioned above which is employed in agriculture, in the greenhouse, in forests or in horticulture. In particular, this takes the form of seed of maize, peanut, canola, oilseed rape, poppy, soya beans, cotton, beet (for example sugar beet and fodder beet), rice, sorghum and millet, wheat, barley, oats, rye, sunflower, tobacco, potato or vegetables (e.g. tomatoes or brassicas). The compositions according to the invention are likewise suitable for treating the seed of fruit plants and vegetables as already mentioned above. The treatment of the seed of maize, soya beans, cotton, wheat and canola or oilseed rape is of particular importance.
  • As already mentioned above, the treatment of transgenic seed with a composition according to the invention is also of particular importance. This takes the form of seed of plants which, as a rule, comprise at least one heterologous gene which governs the expression of a polypeptide with in particular insecticidal properties. In this context, the heterologous genes in transgenic seed may be derived from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. The present invention is particularly suitable for the treatment of transgenic seed which comprises at least one heterologous gene originating from Bacillus sp. and whose gene product shows activity against the European corn borer and/or the corn root worm. It is particularly preferably a heterologous gene derived from Bacillus thuringiensis.
  • Within the scope of the present invention, the active compounds according to the invention is applied to the seed either alone or in a suitable formulation. Preferably, the seed is treated in a state in which it is stable enough to avoid damage during treatment. In general, the seed may be treated at any point in time between harvest and sowing. The seed usually used has been separated from the plant and freed from cobs, shells, stalks, coats, hairs or the flesh of the fruits.
  • When treating the seed, care must generally be taken that the amount of the composition according to the invention applied to the seed and/or the amount of further additives is chosen in such a way that the germination of the seed is not adversely affected, or that the resulting plant is not damaged. This must be borne in mind in particular in the case of active compounds which can have phytotoxic effects at certain application rates.
  • As already mentioned above, it is possible to treat all plants and their parts according to the invention. In a preferred embodiment, wild plant species and plant cultivars, or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and parts thereof, are treated. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering methods, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated. The terms “parts”, “parts of plants” and “plant parts” have been explained above.
  • Particularly preferably, plants of the plant cultivars which are in each case commercially available or in use are treated according to the invention. Plant cultivars are to be understood as meaning plants having novel properties (“traits”) which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be cultivars, bio- or genotypes.
  • Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, diet), the treatment according to the invention may also result in superadditive (“synergistic”) effects. Thus, for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the substances and compositions which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, higher quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
  • The transgenic plants or plant cultivars (obtained by genetic engineering) which are preferably to be treated according to the invention include all plants which, by virtue of the genetic modification, received genetic material which imparted particularly advantageous, useful traits to these plants. Examples of such traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, higher quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products. Further and particularly emphasized examples of such traits are a better defence of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and/or viruses, and also increased tolerance of the plants to certain herbicidally active compounds. Examples of (transgenic) plants which may be mentioned are the important crop plants, such as cereals (wheat, rice), maize, soya beans, potatoes, sugar beet, tomatoes, peas and other vegetable varieties, cotton, tobacco, oilseed rape and also fruit plants (with the fruits apples, pears, citrus fruits and grapes), and particular emphasis is given to maize, soya beans, potatoes, cotton, tobacco and oilseed rape. Traits that are emphasized are in particular increased defence of the plants against insects, arachnids, nematodes and slugs and snails by virtue of toxins formed in the plants, in particular those formed in the plants by the genetic material from Bacillus thuringiensis (for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c, Cry2Ab, Cry3Bb and CryIF and also combinations thereof) (referred to hereinbelow as “Bt plants”). Traits that are also particularly emphasized are the increased defence of the plants against fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins. Traits that are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulphonylureas, glyphosate or phosphinotricin (for example the “PAT” gene). The genes which impart the desired traits in question can also be present in combination with one another in the transgenic plants. Examples of “Bt plants” which may be mentioned are maize varieties, cotton varieties, soya bean varieties and potato varieties which are sold under the trade names YIELD GARD® (for example maize, cotton, soya beans), KnockOut® (for example maize), StarLink® (for example maize), Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato). Examples of herbicide-tolerant plants which may be mentioned are maize varieties, cotton varieties and soya bean varieties which are sold under the trade names Roundup Ready® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link® (tolerance to phosphinotricin, for example oilseed rape), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulphonylureas, for example maize). Herbicide-resistant plants (plants bred in a conventional manner for herbicide tolerance) which may be mentioned include the varieties sold under the name Clearfield® (for example maize). Of course, these statements also apply to plant cultivars having these genetic traits or genetic traits still to be developed, which plant cultivars will be developed and/or marketed in the future.
  • The plants listed can be treated according to the invention in a particularly advantageous manner with the compounds of the formula (I). The preferred ranges stated above for the active compounds also apply to the treatment of these plants. Particular emphasis is given to the treatment of plants with the compounds or mixtures specifically mentioned in the present text.
  • The active compounds according to the invention act not only against plant, hygiene and stored product pests, but also in the veterinary medicine sector against animal parasites (ecto- and endoparasites), such as hard ticks, soft ticks, mange mites, leaf mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, feather lice and fleas. These parasites include:
  • From the order of the Anoplurida, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
  • From the order of the Mallophagida and the suborders Amblycerina and Ischnocerina, for example, Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp.
  • From the order of the Diptera and the suborders Nematocerina and Brachycerina, for example, Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus spp.
  • From the order of the Siphonapterida, for example, Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
  • From the order of the Heteropterida, for example, Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
  • From the order of the Blattarida, for example, Blatta orientalis, Periplaneta americana, Blattela germanica, Supella spp.
  • From the subclass of the Acari (Acarina) and the orders of the Meta- and Mesostigmata, for example, Argas spp., Ornithodorus spp., Otobius spp., Ixodes spp., Amblyomma spp., Boophilus spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp., Dermanyssus spp., Raillietia spp., Pneumonyssus spp., Sternostoma spp., Varroa spp.
  • From the order of the Actinedida (Prostigmata) and Acaridida (Astigmata), for example, Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
  • The active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which infest agricultural productive livestock, such as, for example, cattle, sheep, goats, horses, pigs, donkeys, camels, buffalo, rabbits, chickens, turkeys, ducks, geese and bees, other pets, such as, for example, dogs, cats, caged birds and aquarium fish, and also so-called test animals, such as, for example, hamsters, guinea pigs, rats and mice. By controlling these arthropods, cases of death and reduction in productivity (for meat, milk, wool, hides, eggs, honey etc.) should be diminished, so that more economic and easier animal husbandry is possible by use of the active compounds according to the invention.
  • The active compounds according to the invention are used in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, potions, drenches, granules, pastes, boluses, the feed-through process and suppositories, by parenteral administration, such as, for example, by injection (intramuscular, subcutaneous, intravenous, intraperitoneal and the like), implants by nasal administration, by dermal use in the form, for example, of dipping or bathing, spraying, pouring on and spotting on, washing and powdering, and also with the aid of moulded articles containing the active compound, such as collars, ear marks, tail marks, limb bands, halters, marking devices and the like.
  • When used for cattle, poultry, pets and the like, the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, free-flowing compositions), which comprise the active compounds in an amount of 1 to 80% by weight, directly or after 100 to 10 000-fold dilution, or they can be used as a chemical bath.
  • It has furthermore been found that the compounds according to the invention also have a strong insecticidal action against insects which destroy industrial materials.
  • The following insects may be mentioned as examples and as preferred—but without any limitation:
  • Beetles, such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthes rugicollis, Xyleborus spec., Tryptodendron spec., Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec., Dinoderus minutus;
  • Hymenopterons, such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur;
  • Termites, such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus;
  • Bristletails, such as Lepisma saccharina.
  • Industrial materials in the present connection are to be understood as meaning non-living materials, such as, preferably, plastics, adhesives, sizes, papers and cardboards, leather, wood and processed wood products and coating compositions.
  • The ready-to-use compositions may, if appropriate, comprise further insecticides and, if appropriate, one or more fungicides.
  • With respect to possible additional additives, reference may be made to the insecticides and fungicides mentioned above.
  • The compounds according to the invention can likewise be employed for protecting objects which come into contact with saltwater or brackish water, such as hulls, screens, nets, buildings, moorings and signalling systems, against fouling.
  • Furthermore, the compounds according to the invention, alone or in combination with other active compounds, may be employed as antifouling agents.
  • In domestic, hygiene and stored-product protection, the active compounds are also suitable for controlling animal pests, in particular insects, arachnids and mites, which are found in enclosed spaces such as, for example, dwellings, factory halls, offices, vehicle cabins and the like. They can be employed alone or in combination with other active compounds and auxiliaries in domestic insecticide products for controlling these pests. They are active against sensitive and resistant species and against all developmental stages. These pests include:
  • From the order of the Scorpionidea, for example, Buthus occitanus.
  • From the order of the Acarina, for example, Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.
  • From the order of the Araneae, for example, Aviculariidae, Araneidae.
  • From the order of the Opiliones, for example, Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
  • From the order of the Isopoda, for example, Oniscus asellus, Porcellio scaber.
  • From the order of the Diplopoda, for example, Blaniulus guttulatus, Polydesmus spp.
  • From the order of the Chilopoda, for example, Geophilus spp.
  • From the order of the Zygentoma, for example, Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus.
  • From the order of the Blattaria, for example, Blatta orientalies, Blattella germanica, Blattella asahinai, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta australasiae, Periplaneta americana, Periplaneta brunnea, Periplaneta fuliginosa, Supella longipalpa.
  • From the order of the Saltatoria, for example, Acheta domesticus.
  • From the order of the Dermaptera, for example, Forficula auricularia.
  • From the order of the Isoptera, for example, Kalotermes spp., Reticulitermes spp.
  • From the order of the Psocoptera, for example, Lepinatus spp., Liposcelis spp.
  • From the order of the Coleoptera, for example, Anthrenus spp., Attagenus spp., Dermestes spp., Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum.
  • From the order of the Diptera, for example, Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria, Simulium spp., Stomoxys calcitrans, Tipula paludosa.
  • From the order of the Lepidoptera, for example, Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.
  • From the order of the Siphonaptera, for example, Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.
  • From the order of the Hymenoptera, for example, Camponotus herculeanus, Lasius faliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitam.
  • From the order of the Anoplura, for example, Pediculus humanus capitis, Pediculus humanus corporis, Pemphigus spp., Phylloera vastatrix, Phthirus pubis.
  • From the order of the Heteroptera, for example, Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans.
  • In the field of household insecticides, they are used alone or in combination with other suitable active compounds, such as phosphoric esters, carbamates, pyrethroids, neonicotinoids, growth regulators or active compounds from other known classes of insecticides.
  • They are used in aerosols, pressure-free spray products, for example pump and atomizer sprays, automatic fogging systems, foggers, foams, gels, evaporator products with evaporator tablets made of cellulose or polymer, liquid evaporators, gel and membrane evaporators, propeller-driven evaporators, energy-free, or passive, evaporation systems, moth papers, moth bags and moth gels, as granules or dusts, in baits for spreading or in bait stations.
    • PREPARATION EXAMPLES Example 1 Precursor 6-Chloro-N-methylpyrimidine-4,5-diamine
  • Figure US20120071496A1-20120322-C00007
  • 5-Amino-4,6-dichloropyrimidine (15.0 g, 91.4 mmol) and methylamine (2M solution in THF, 5 eq) were initially charged, and triethylamine (27.76 g, 274 mmol) was added. The mixture was stirred under reflux until the conversion was complete (about 3 hours). The reaction mixture was then concentrated, and water was added to the residue. The pH was adjusted to 7-8 using saturated NaHCO3 solution. The mixture was extracted 3× with methylene chloride, the combined organic phases were dried over sodium sulphate and filtered and the solvent was removed under reduced pressure.
  • Yield: 12.0 g (82%)
  • LC-MS: M+(ES+) 159 (100%)
  • NMR DMSO 2.89 (3H, m), 4.77 (2H, s), 6.71 (1H, s), 7.75 (1H, s).
    • Example 2 Precursor N-(4-Chloro-6-cyclopropylaminopyrimidin-5-yl)-2-ethylnicotinamide
  • Figure US20120071496A1-20120322-C00008
  • 6-Chloro-N-cyclopropylpyrimidine-4,5-diamine (cf. Journal of Combinatorial Chemistry (2003), 5(5), 653-659) (3.0 g, 16.2 mmol) was initially charged in a mixture of methylene chloride (12.20 ml) and pyridine (3.94 ml). The suspension was cooled to 0° C., and solid 2-ethylnicotinoyl chloride (1.2 eq) was added. The reaction mixture was allowed to warm to room temperature and stirred until the reaction had gone to completion. 10 ml of methylene chloride were then added, the suspension turning into a solution. About 10 ml of semisaturated NaHCO3 solution were added to the organic phase whilst the mixture was stirred vigorously in a flask using a magnetic stirrer; poorly soluble crystals (product) precipitated and were filtered off with suction, washed 3× with a little water and 3× with n-heptane and dried.
  • Fraction 1: 3.41 g, 66%
  • LC/MS: M+(ES+)=318 (100%)
  • NMR 0.56 (2H, m), 0.76 (2H, m), 1.25 (3H, t), 2.87 (1H, m), 2.96 (2H, q), 7.22 (1H, s), 7.32 (1H, m), 8.10 (1H, m), 8.30 (1H, m), 8.59 (1H, m), 9.5.5 (1H, m).
    • Example 3 End Product N-[4-Cyclopropylamino-6-(2,4-dichlorophenyl)pyrimidin-5-yl]-2-ethylnicotinamide
  • Figure US20120071496A1-20120322-C00009
  • In a test tube which had been dried by heating and preheated to 100° C., the degassed diluent mixture dioxane (2 ml)/water (0.7 ml) was added to N-(4-chloro-6-cyclopropylaminopyrimidin-5-yl)-2-ethylnicotinamide (0.41 mmol), sodium carbonate (3 eq) and 2,4-dichlorophenylboronic acid (2 eq). 5 mol % of tetrakis(triphenylphosphine)palladium(0) were added, and the reaction mixture was stirred at 90° C. for 3 hours. The mixture was then diluted with water and extracted 3× with methylene chloride, and the combined organic phases were washed with aqueous NaHCO3 solution, dried over Na2SO4, filtered and concentrated under reduced pressure.
  • LC/MS: M+(ES+)=430 (50%) NMR DMSO 0.57 (2H, m), 0.79 (2H, m), 1.03 (3H, t), 2.91 (1H, m), 6.86 (1H, m), 7.263 (1H, m), 7.44 (2H, m), 7.61 (1H, m), 7.72 (1H, m), 8.50 (2H, m), 9.33 (1H, s).
  • The residue was separated on a Companion using a Chromabond Flash RS 70 SiOH cartrige and methylene chloride/MeOH.
  • LC/MS: M+(ES+)=428 (100%)
    • Example 4 Precursor 6-(4-Chlorophenyl)-N-cyclopropylpyrimidine-4,5-diamine
  • Figure US20120071496A1-20120322-C00010
  • In a reactor carousel test tube which had been dried by heating and preheated to 100° C., the degassed diluent mixture dioxane (20 ml)/water (7 ml) was added to 6-chloro-N-cyclopropylpyrimidine-4,5-diamine (10 g, 54.1 mmol) and sodium carbonate (17.22 g, 162 mmol). 5 mol % of tetrakis(triphenylphosphine)palladium(0) and 4-chlorophenylboronic acid (108.2 mmol) were added, and the reaction mixture was stirred at 90° C. overnight. The solution was cooled, filtered and concentrated and the residue was recrystallised from acetonitrile.
  • Yield: 8193 mg; 58%
  • LC-MS: M+(ES)=261 (100%)
  • NMR DMSO 0.52 (2H, m), 0.53 (2H, m), 2.89 (1H m), 4.52 (1H, s), 6.76 (1H, s), 7.47 (2H, m), 7.65 (2H, m), 8.04 1H, s).
    • Example 5 End Product N-[4-(4-Chlorophenyl)-6-cyclopropylaminopyemidin-5-yl]-2-ethylnicotinamide
  • Figure US20120071496A1-20120322-C00011
  • 6-(4-Chlorophenyl)-N-cyclopropylpyrimidine-4,5-diamine (1.00 g, 3.83 mmol) was initially charged in a mixture of DCM (3.20 ml) and pyridine (0.93 ml) and cooled to 0° C. Solid 2-ethylnicotinoyl chloride (780 mg, 4.60 mmol) was added, and the reaction mixture was warmed to room temperature and stirred for another hour. After addition of semisaturated NaHCO3 solution, the organic phase was separated off and concentrated under reduced pressure.
  • The residue was separated on a Companion using a Chromabond Flash RS 120 SiOH cartrige and DCM/MeOH.
  • Fraction 1: 394 mg; 25%
  • LC/MS: M+(ES+)=394 (98%) NMR DMSO 0.55 (2H, m), 0.78 (2H, m), 1.063 (31-1, t), 2.89 (1H, m), 6.94 (1H, s), 7.28 (1H, m), 7.45 (2H, d), 7.67 (211, d), 7.88 (1H, d), 8.52 (2H, m), 9.37 (1H, s).
    • Example 6 6-Chloro-N4-[4-(trifluoromethyl)phenyl]pyrimidine-4,5-diamine
  • (cf. also Tetrahedron Letters, 48, 1489 (2007))
  • Figure US20120071496A1-20120322-C00012
  • A mixture of 4,6-dichloroaminopyrimidine (1.5 g), isopropanol (20 ml), 4-trifluoromethylaniline (1.47 g) and a drop of conc. aqueous hydrochloric acid was heated in a microwave vessel at 150° C. for 10 min. After cooling, the precipitate obtained was filtered off.
  • Yield 580 mg.
    • Example 7 N-(4-Chloro-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-5-yl)-2-ethylnicotinamide
  • Figure US20120071496A1-20120322-C00013
  • The compound from Example 6 (349 mg) was initially charged in a mixture of methylene chloride (3 ml) and pyridine (0.35 ml). The suspension was cooled to 0° C., and solid 2-ethylnicotinoyl chloride (1.2 eq) was added. The reaction mixture was allowed to warm to room temperature and stirred until the reaction had gone to completion. 10 ml of methylene chloride were then added, the suspension turning into a solution. After addition of semisaturated NaHCO3 solution, the mixture was stirred and the organic phase was separated off and concentrated under reduced pressure.
  • The residue was separated on a Companion using a Chromabond Flash RS 120 SiOH cartrige and hexane/ethyl acetate.
  • Fraction 1: 240 mg; 38%
  • Other compounds according to the invention are listed in the table below.
  • The following abbreviations are used:
  • Ph=Phenyl=Ar
  • R in column R1 (cf., for example, Ex. Nos. 1-222, 1-229, 1-230, 1-250, 3-7 etc.) denotes the point of attachment to the remainder of the molecule.
    • 08-3106 Foreign Countries
  • TABLE 1
    Compounds of the formula
    Figure US20120071496A1-20120322-C00014
    Ex.
    No. R1 R7 G1 G2 G3 R6 A G4 G5 G6
    1-1  cyclopropyl CH3 4-F H H H N H H H
    1-2  cyclopropyl CH3
    Figure US20120071496A1-20120322-C00015
         		H H H N H H H
    1-3  cyclopropyl CH3
    Figure US20120071496A1-20120322-C00016
         		H H H N H H H
    1-4  cyclopropyl CH2CH3 3-F 4-F H H N H H H
    1-5  cyclopropyl CH2CH3 2-F 4-F H H N H H H
    1-6  cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00017
         		H H H N H H H
    1-7  cyclopropyl CH2CH3 4-OCH3 H H H N H H H
    1-8  cyclopropyl CH2CH3 4-CH3 H H H N H H H
    1-9  cyclopropyl CH2CH3 2-F 3-F H H N H H H
    1-10  cyclopropyl CH2CH3 4-SCH3 H H H N H H H
    1-11  cyclopropyl CH2CH3 2-F H H H N H H H
    1-12  cyclopropyl CH2CH3 3,4-OCH2CH2—O— H H N H H H
    1-13  cyclopropyl CH2CH3 3-Cl H H H N H H H
    1-14  cyclopropyl CH2CH3 3-NH2 H H H N H H H
    1-15  cyclopropyl CH2CH3 3-F 4-F 5-F H N H H H
    1-16  cyclopropyl CH2CH3 2-F 3-F 4-F H N H H H
    1-17  cyclopropyl CH2CH3 4-COCH3 H H H N H H H
    1-18  cyclopropyl CH2CH3 4-C(CH3)3 H H H N H H H
    1-19  cyclopropyl CH2CH3 4-N(CH3)2 H H H N H H H
    1-20  cyclopropyl CH2CH3 3-Cl 4-F H H N H H H
    1-21  CH(CH3)2 CH2CH3 4-F H H H N H H H
    1-22  CH(CH3)2 CH2CH3 4-OCF3 H H H N H H H
    1-23  CH(CH3)CH2SCH3 CH2CH3 4-OCF3 H H H N H H H
    1-24  CH(CH3)CH2SCH3 CH2CH3 4-F H H H N H H H
    1-25  cyclopropyl CH2CH3 2-F 3-Cl H H N H H H
    1-26  cyclopropyl CH2CH3 3,4-OCF2O H H N H H H
    1-27  cyclopropyl CH2CH3 3-CH3 4-F H H N H H H
    1-28  cyclopropyl CH2CH3 3-C(CH3)NOCH3 H H H N H H H
    1-29  cyclopropyl CH2CH3 3-CHNOCH3 H H H N H H H
    1-30  cyclopropyl CH2CH3 2-F 5-CF3 H H N H H H
    1-31  cyclopropyl CH2CH3 CONH2 H H H N H H H
    1-32  cyclopropyl CH2CH3 3,4-OCH2CH2O— H H N H H H
    1-33  cyclopropyl CH2CH3 3-NH2 OCF3 5-NH2 H N H H H
    1-34  cyclopropyl CH2CH3 4-CO2CH3 H H H N H H H
    1-35  cyclopropyl CH2CH3 3-SCH3 H H H N H H H
    1-36  cyclopropyl CH2CH3 4-CH2OCH3 H H H N H H H
    1-37  cyclopropyl CH2CH3 2-F 4-F 5-Cl H N H H H
    1-38  cyclopropyl CH2CH3 3-CH2OCH3 H H H N H H H
    1-39  cyclopropyl CH2CH3 4-NHCOCH3 H H H N H H H
    1-40  cyclopropyl CH2CH3 3-F 4-NH2 H H N H H H
    1-41  cyclopropyl CH2CH3 3-F 4-OCH3 H H N H H H
    1-42  cyclopropyl CH2CH3 3-F 4-CH3 H H N H H H
    1-43  cyclopropyl CH2CH3 2-F 4-CF3 H H N H H H
    1-44  cyclopropyl CH2CH3 3-F 4-Cl H H N H H H
    1-45  cyclopropyl CH2CH3 2-F 5-COCH3 H H N H H H
    1-46  cyclopropyl CH2CH3 3-F 5-OCH3 H H N H H H
    1-47  cyclopropyl CH2CH3 2-F 5-CH3 H H N H H H
    1-48  cyclopropyl CH2CH3 2-F 4-OCH3 H H N H H H
    1-49  cyclopropyl CH2CH3 3-F 5-Cl H H N H H H
    1-50  cyclopropyl CH2CH3 3-S(O)2CH3 H H H N H H H
    1-51  cyclopropyl CH2CH3 3-CN 4-F H H N H H H
    1-52  cyclopropyl CH2CH3 2-F 3-OCH3 H H N H H H
    1-53  cyclopropyl CH2CH3 3-Si(CH3)3 H H H N H H H
    1-54  cyclopropyl CH2CH3 2-OCH3 4-F H H N H H H
    1-55  cyclopropyl CH2CH3 3-NO2 H H H N H H H
    1-56  cyclopropyl CH2CH3 2-Cl 5-Cl H H N H H H
    1-57  cyclopropyl CH2CH3 3-CH3 5-CH3 H H N H H H
    1-58  cyclopropyl CH2CH3 3-Ar H H H N H H H
    1-59  cyclopropyl CH2CH3 2-Cl 5-Cl H H N H H H
    1-60  cyclopropyl CH2CH3 4-CH2CH2 H H H N H H H
    1-61  cyclopropyl CH2CH3 2-Cl 3-Cl H H N H H H
    1-62  cyclopropyl CH2CH3 4-Ar H H H N H H H
    1-63  cyclopropyl CH2CH3 3-CH3 4-CH3 H H N H H H
    1-64  cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00018
         		H H H N H H H
    1-65  cyclopropyl CH2CH3 2-F 4-OCH3 5-F H N H H H
    1-66  cyclopropyl CH2CH3 3-NH(SO2)CH3 H H H N H H H
    1-67  cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00019
         		H H H N H H H
    1-68  cyclopropyl CH2CH3 4-OCH(CH3) H H H N H H H
    1-69  cyclopropyl CH2CH3 3-Cl 4-Cl 5-Cl H N H H H
    1-70  cyclopropyl CH2CH3 4-NO2 H H H N H H H
    1-71  cyclopropyl CH2CH3 3-F 5-NH2 H H N H H H
    1-72  cyclopropyl CH3 4-OCF3 H H H CH H H H
    1-73  cyclopropyl CH2CH3 4-OCF3 H H H N H H H
    1-74  CH(CH3)2 CH3 4-OCF3 H H H N H H H
    1-75  cyclopropyl Cl 4-OCF3 H H H N H H H
    1-76  CH(CH3)2 Cl 4-OCF3 H H H N H H H
    1-77  CH(CH3)2 CH3 4-OCF3 H H H CH H H H
    1-78  CH(CH3)2 H OCF3 H H H CH H H H
    1-79  CH(CH3)2 Cl 4-OCF3 H H H CH H H H
    1-80  cyclopropyl Cl 4-CF3 H H H CH H H H
    1-81  cyclopropyl CH3 4-CF3 H H H CH H H H
    1-82  cyclopropyl Cl 4-CF3 H H H N H H H
    1-83  cyclopropyl CH3 4-CF3 H H H N H H H
    1-84  cyclopropyl CF3 4-CF3 H H H N H H H
    1-85  cyclopropyl CH(CH3)2 4-CF3 H H H N H H H
    1-86  cyclopropyl CH2CH3 4-CF3 H H H CH H H H
    1-87  cyclopropyl CH3 4-CF3 H H CH3 N H H H
    1-88  cyclopropyl Cl 4-CF3 H H CH3 CH H H H
    1-89  cyclopropyl CH3 4-CF3 H H cyclopropyl N H H H
    1-90  CH(CH3)2 CH3 4-OCF3 H H H N H H H
    1-91 
    Figure US20120071496A1-20120322-C00020
         		CH3 4-OCF3 H H H N H H H
    1-92  CH(CH3)CH2CH3 CH3 4-OCF3 H H H N H H H
    1-93  cyclopropyl CH3 4-OCF3 H H H N H H H
    1-94  CH(CH3)2 CH3 4-OCF3 H H H N H H H
    1-95 
    Figure US20120071496A1-20120322-C00021
         		CH3 4-OCF3 H H H N H H H
    1-96  cyclopropyl CH3 4-OCF3 H H H N H H H
    1-97  cyclopropyl CH3 4-OCF3 H H C(CH3) N H H H
    1-98  cyclopropyl CH3 4-OCF3 H H 4-Cl—Ph N H H H
    1-99 
    Figure US20120071496A1-20120322-C00022
         		Cl 4-OCF3 H H H N H H H
    1-100
    Figure US20120071496A1-20120322-C00023
         		CH3 4-OCF3 H H H N H H H
    1-101 CH(CH3)CH2CH3 CH3 4-OCF3 H H H N H H H
    1-102 CH(CH3)CH2CH3 Cl 4-OCF3 H H H N H H H
    1-103
    Figure US20120071496A1-20120322-C00024
         		CH3 4-OCF3 H H H N H H H
    1-104
    Figure US20120071496A1-20120322-C00025
         		Cl 4-OCF3 H H H N H H H
    1-105 C(CH3)3 Cl 4-OCF3 H H H N H H H
    1-106 CH(CH2CH3)2 CH3 4-OCF3 H H H N H H H
    1-107 CH(CH2CH3)3 Cl 4-OCF3 H H H N H H H
    1-108 CH(CH3)CH(CH3)2 CH3 4-OCF3 H H H N H H H
    1-109 CH(CH3)CH(CH3)3 Cl 4-OCF3 H H H N H H H
    1-110
    Figure US20120071496A1-20120322-C00026
         		CH3 4-OCF3 H H H N H H H
    1-111
    Figure US20120071496A1-20120322-C00027
         		Cl 4-OCF3 H H H N H H H
    1-112 cyclopropyl H 4-OCF3 H H H CH H H H
    1-113 cyclopropyl Cl 4-OCF3 H H H CH H H H
    1-114 cyclopropyl CH2CH3 4-SCF3 H H H N H H H
    1-115 cyclopropyl CH2CH3 3-NH2 4- OCH(CH3)2 H H N H H H
    1-116 cyclopropyl CH3 4-SCF3 H H H N H H H
    1-117 cyclopropyl CH3 S(O)CF3 H H H N H H H
    1-118 cyclopropyl CH3 S(O)CHF2 H H H N H H H
    1-119 cyclopropyl CH3
    Figure US20120071496A1-20120322-C00028
         		H H H N H H H
    1-120 cyclopropyl CH3 OCF3 CH3 H H N H H H
    1-121 cyclopropyl CH3 4-OSO2CH(CH3)2 H H H N H H H
    1-122 cyclopropyl CH3 3-F 4-CF3 5-F H N H H H
    1-123 cyclopropyl CH3 4-OCF2CHFCF3 4-CF3 H H N H H H
    1-124 cyclopropyl CH2CH3 4-F H H H N H H H
    1-125 CH3 CH2CH3 4-F H H H N H H H
    1-126 cyclopropyl CH2CH3 2-Cl 4-Cl H H N H H H
    1-127 cyclopropyl CH2CH3 H H H H N H H H
    1-128 cyclopropyl H H H H H N H H H
    1-129 cyclopropyl Cl 4-F H H H N H H H
    1-130 cyclopropyl Cl 4-Cl H H H N H H H
    1-131 cyclopropyl Br 4-Cl H H H N H H H
    1-132 cyclopropyl Br 4-F H H H N H H H
    1-133 cyclopropyl CH2CH3 4-CN H H H N H H H
    1-134 C(CH3)3 CH2CH3 4-F H H H N H H H
    1-135 C(CH3)3 CH2CH3 4-Cl H H H N H H H
    1-136 C(CH3)3 CH2CH3 4-CN H H H N H H H
    1-137 C(CH3)3 CH2CH3 4-CF3 H H H N H H H
    1-138 C(CH3)3 CH2CH3 OCF3 H H H N H H H
    1-139 cyclopropyl CH2CH3 2-Cl 4-F H H N H H H
    1-140 cyclopropyl CH2CH3 2-Cl H H H N H H H
    1-141 C(CH3)3 CH2CH3 3-NH2 4-F H H N H H H
    1-142 C(CH3)3 CH2CH3 2-Cl 4-Cl H H N H H H
    1-143
    Figure US20120071496A1-20120322-C00029
         		CH2CH3 4-F H H H N H H H
    1-144
    Figure US20120071496A1-20120322-C00030
         		CH2CH3 4-Cl H H H N H H H
    1-145
    Figure US20120071496A1-20120322-C00031
         		CH2CH3 4-CN H H H N H H H
    1-146
    Figure US20120071496A1-20120322-C00032
         		CH2CH3 4-OCF3 H H H N H H H
    1-147
    Figure US20120071496A1-20120322-C00033
         		CH2CH3 4-F H H H N H H H
    1-148
    Figure US20120071496A1-20120322-C00034
         		CH2CH3 2-Cl 4-Cl H H N H H H
    1-149
    Figure US20120071496A1-20120322-C00035
         		CH2CH3 4-Cl H H H N H H H
    1-150
    Figure US20120071496A1-20120322-C00036
         		CH2CH3 4-CN H H H N H H H
    1-151
    Figure US20120071496A1-20120322-C00037
         		CH2CH3 4-Cl H H H N H H H
    1-152
    Figure US20120071496A1-20120322-C00038
         		CH2CH3 H H H H N H H H
    1-153 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00039
         		H H H N H H H
    1-154 cyclopropyl OCH3 4-Cl H H H N H H H
    1-155 cyclopropyl OCH3 4-F H H H N H H H
    1-156 cyclopropyl OCH3 4-CN H H H N H H H
    1-157 cyclopropyl OCH3 4-OCF3 H H H N H H H
    1-158 cyclopropyl OCH2CH3 4-Cl H H H N H H H
    1-159 cyclopropyl OCH2CH3 4-F H H H N H H H
    1-160 cyclopropyl OCH2CH3 4-CN H H H N H H H
    1-161 cyclopropyl OCH2CH3 4-OCF3 H H H N H H H
    1-162 cyclopropyl O(CH3)2 4-Cl H H H N H H H
    1-163 cyclopropyl OCH(CH3)2 4-F H H H N H H H
    1-164 cyclopropyl OCH(CH3)2 4-CN H H H N H H H
    1-165 cyclopropyl OCH(CH3)2 4-OCF3 H H H N H H H
    1-166 cyclopropyl OCH2CF3 4-Cl H H H N H H H
    1-167 cyclopropyl OCH2CF3 4-F H H H N H H H
    1-168 cyclopropyl OCH2CF3 4-CN H H H N H H H
    1-169 cyclopropyl OCH2CF3 4-OCF3 H H H N H H H
    1-170 cyclopropyl CF3 4-F H H H N H H H
    1-171 cyclopropyl CN 4-F H H H N H H H
    1-172 cyclopropyl
    Figure US20120071496A1-20120322-C00040
         		4-H H H H N H H H
    1-173 cyclopropyl
    Figure US20120071496A1-20120322-C00041
         		4-Cl H H H N H H H
    1-174 cyclopropyl CHFCH3 4-Cl H H H N H H H
    1-175 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00042
         		H H H N H H H
    1-176 cyclopropyl CH2CF3 4-Cl H H H N H H H
    1-177 cyclopropyl CH2CH3 4-Cl H H H N H H H
    1-178 cyclopropyl CF3 4-Cl H H H N H H H
    1-179 cyclopropyl CF2H 4-Cl H H H N H H H
    1-180 cyclopropyl CH2CH3 2-CH3 4-F H H N H H H
    1-181 cyclopropyl CH2CH3 2-CH3 4-CN H H N H H H
    1-182 cyclopropyl CH2CH3 2-CH3 H H H N H H H
    1-183 cyclopropyl CH2CH3 2-CH3 3-NH2 4-F H N H H H
    1-184 cyclopropyl CH2CH3 2-CH3 5-F H H N H H H
    1-185 cyclopropyl CH2CH3 4-OCF3 H H H N H H H
    1-186 cyclopropyl CH2CH3 4-CF3 H H H N H H H
    1-187 cyclopropyl CH2CH3 2-F 4-Cl H H N H H H
    1-188 cyclopropyl CH2CH3 2-CH3 4-Cl H H N H H H
    1-189 cyclopropyl CH2CH3 2-CH3 4-CF3 H H N H H H
    1-190 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00043
         		H H H N H H H
    1-191 cyclopropyl CH2CH3 2-CH3 4-OCF3 H H N H H H
    1-192 cyclopropyl CH2CH3 4-Cl H H H N H H H
    1-193 cyclopropyl CH3 4-OCF3 H H H N CF3 H H
    1-194 cyclopropyl CHFCH3 4-Cl H H H N H Cl H
    1-195 cyclopropyl CH3 4-Cl H H H N CH3 H CH3
    1-196 cyclopropyl CH2CH3 4-F H H H N CF3 H H
    1-197 cyclopropyl cyclopropyl 4-Cl H H H N H Cl H
    1-198 cyclopropyl cyclopropyl 4-F H H H N H Cl H
    1-199 cyclopropyl CH3 4-Cl H H H N CF3 H H
    1-200 cyclopropyl CH2CH3 4-Cl H H H N H H CF3
    1-201 cyclopropyl CH2CH3 4-F H H H N H H CF3
    1-202 cyclopropyl CH2CH3 4-CN H H H N H H CF3
    1-203 cyclopropyl CH2CH3 4-CF3 H H H N H H CF3
    1-204 cyclopropyl CH2CH3 4-OCF3 H H H N H H CF3
    1-205 cyclopropyl CH2CH3 2-F 4-F H H N H H CF3
    1-206 cyclopropyl CH2CH3 2-Cl 4-Cl H H N H H CF3
    1-207 cyclopropyl CH3 4-Cl H H H N H H CF3
    1-208 cyclopropyl CH3 4-F H H H N H H CF3
    1-209 cyclopropyl CH3 4-CN H H H N H H CF3
    1-210 cyclopropyl CH3 4-CF3 H H H N H H CF3
    1-211 cyclopropyl CH3 4-OCF3 H H H N H H CF3
    1-212 cyclopropyl CH3 2-F 4-F H H N H H CF3
    1-213 cyclopropyl CH3 2-Cl 4-Cl H H N H H CF3
    1-214 cyclopropyl cyclopropyl 4-Cl H H H N H H CF3
    1-215 cyclopropyl cyclopropyl 4-F H H H N H H CF3
    1-216 cyclopropyl cyclopropyl 4-CN H H H N H H CF3
    1-217 cyclopropyl cyclopropyl 4-CF3 H H H N H H CF3
    1-218 cyclopropyl cyclopropyl 4-OCF3 H H H N H H CF3
    1-219 cyclopropyl cyclopropyl 2-F 4-F H H N H H CF3
    1-220 cyclopropyl cyclopropyl 2-Cl 4-Cl H H N H H CF3
    1-221 CH(CH3)2 CH2CH3 4-Cl H H H N H H H
    1-222
    Figure US20120071496A1-20120322-C00044
         		CH2CH3 2-F 4-F H H N H H H
    1-223 CH(CH3)CH2SCH3 CH2CH3 4-Cl H H H N H H H
    1-224 cyclobutyl CH2CH3 4-F H H H N H H H
    1-225 cyclobutyl CH2CH3 2-F 4-F H H N H H H
    1-226 cyclobutyl CH2CH3 4-Cl H H H N H H H
    1-227 cyclopentyl CH2CH3 4-F H H H N H H H
    1-228 cyclopentyl CH2CH3 2-F 4-F H H N H H H
    1-229
    Figure US20120071496A1-20120322-C00045
         		CH2CH3 4-F H H H N H H H
    1-230
    Figure US20120071496A1-20120322-C00046
         		CH2CH3 2-F 4-Cl H H N H H H
    1-231 cyclobutyl CH2CH3 2-F 4-Cl H H N H H H
    1-232 cyclopropyl CH2CH3 4-iC3F7 H H H N H H H
    1-233 cyclopropyl cyclopropyl 4-iC3F7 H H H N H H H
    1-234 cyclopropyl cyclopropyl H H H H N H H H
    1-235 cyclopropyl cyclopropyl 4-F H H H N H H H
    1-236 cyclopropyl cyclopropyl 4-Cl H H H N H H H
    1-237 cyclopropyl propyl H H H H N H H H
    1-238 cyclopropyl propyl 4-F H H H N H H H
    1-239 cyclopropyl propyl 4-Cl H H H N H H H
    1-240 cyclopropyl cyclopropyl 2-F 4-F H H N H H H
    1-241 cyclopropyl C2F5 4-Cl H H H N H H H
    1-242 cyclopropyl cyclopropyl 4-CN H H H N H H H
    1-243 cyclopropyl cyclopropyl 4-OCF3 H H H N H H H
    1-244 cyclopropyl propyl 2-Cl 4-Cl H H N H H H
    1-245 cyclopropyl propyl 2-F 4-F H H N H H H
    1-246 cyclopropyl propyl 4-CN H H H N H H H
    1-247 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00047
         		H H H N H H H
    1-248 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00048
         		H H H N H H H
    1-249 cyclopropyl C3F7 4-Cl H H H N H H H
    1-250
    Figure US20120071496A1-20120322-C00049
         		CH2CH3 4-Cl H H H N H H H
    1-251 cyclopropyl C3F7 4-F H H H N H H H
    1-252 cyclopropyl cyclopropyl
    Figure US20120071496A1-20120322-C00050
         		H H H N H H H
    1-253 cyclopropyl cyclopropyl
    Figure US20120071496A1-20120322-C00051
         		H H H N H H H
    1-254 cyclopropyl CH2CF3 2-F 4-F H H N H H H
    1-255 cyclopropyl CH2CH3 4-F H H H CH H H H
    1-256 cyclopropyl CH2CH3 4-Cl H H H CH H H H
    1-257 cyclopropyl CH2CH3 4-OCF3 H H H CH H H H
    1-258 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00052
         		H H H N H H H
    1-259 cyclopropyl cyclopropyl
    Figure US20120071496A1-20120322-C00053
         		H H H N H H H
    1-260 cyclopropyl C2F5 2-F 4-F H H N H H H
    1-261 cyclopropyl C2F5 4-F H H H N H H H
    1-262 cyclopropyl C(═O)NHCH(CH2)2 4-F H H H N H H H
    1-263 cyclopropyl Cl 4-Cl H H H CH H H F
    1-264 cyclopropyl CH2CH2CH3
    Figure US20120071496A1-20120322-C00054
         		H H H N H H H
    1-265 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00055
         		H H H CH H H H
    1-266 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00056
         		H H H N H H H
    1-267 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00057
         		H H H N H H H
    1-268 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00058
         		H H H N H H H
    1-269 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00059
         		H H H N H H H
    1-270 cyclopropyl CH2CH3 2-F 4-F H SCH3 N H H H
    1-271 cyclopropyl OCF3 2-F 4-F H H N H H H
    1-272 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00060
         		H H H N H H H
    1-273 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00061
         		H H H N H H H
    1-274 CH(CF3)CH3 CH2CH3 2-F 4-F H H N H H H
    1-275 cyclopropyl CH2CH3 H H H CH3 N H H H
    1-276 cyclopropyl CH2CH3 4-F H H CH3 N H H H
    1-277 cyclopropyl CH2CH3 2-Cl 4-Cl H CH3 N H H H
    1-278 cyclopropyl CH2CH3 2-F 4-F H CH3 N H H H
    1-279 cyclopropyl CH2CH3 4-OCF3 H H CH3 N H H H
    1-280 cyclopropyl CH2CH3 H H H CH3 CH H H H
    1-281 cyclopropyl CH2CH3 4-F H H CH3 N H H H
    1-282 cyclopropyl CH2CH3 4-Cl H H CH3 N H H H
    1-283 cyclopropyl CH2CH3 2-Cl 4-Cl H CH3 N H H H
    1-284 cyclopropyl CH2CH3 2-Cl 4-Cl H CH3 N H H H
    1-285 cyclopropyl CH2CH3 2-Cl 4-Cl H CH3 N H H H
    1-286 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00062
         		H H H CH H H H
    1-287 cyclopropyl cyclopropyl
    Figure US20120071496A1-20120322-C00063
         		H H H N H H H
    1-288 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00064
         		H H H N H H H
    1-289 cyclopropyl CH2CH3 4-CN H H CH3 N H H H
    1-290 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00065
         		H H SCH3 N H H H
    1-291 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00066
         		H H H CH H H H
    1-292 cyclopropyl cyclopropyl
    Figure US20120071496A1-20120322-C00067
         		H H H N H H H
    1-293 cyclopropyl CH2CH3 4-CN H H H CH H H H
    1-294 CH(CH3)2 CH2CH3 2-F 4-F H H CH H H H
    1-295 cyclopropyl CH2CH3 2-F 4-F H H CH H H H
    1-296 cyclopropyl CH2CH3 H H H H CH H H H
    1-297 CH(CH3)2 CH2CH3 4-OCF3 H H H CH H H H
    1-298 cyclopropyl CH2CH3 2-Cl 4-Cl H H CH H H H
    1-299 CH(CF3)CH3 CH2CH3 4-F H H H N H H H
    1-300 cyclopropyl CH2CH3 2-Cl 4-Cl H CH3 CH H H H
    1-301 cyclopropyl CH2CH3 4-Cl H H CH3 N H H H
    1-302 cyclopropyl CF3 4-Cl H H CH3 CH Cl H H
    1-303 cyclopropyl CH3 4-F H H CH3 CH Cl H H
    1-304 cyclopropyl CH3 4-Cl H H CH3 CH Cl H H
    1-305 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00068
         		H H H N H H H
    1-306 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00069
         		H H H N H H H
    1-307 cyclopropyl CH2CF3 4-F H H H N H H H
    1-308 cyclopropyl CHFCF3 4-F H H H N H H H
    1-309 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00070
         		H H H N H H H
    1-310 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00071
         		H H H N H H H
    1-311 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00072
         		H H H N H H H
    1-312 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00073
         		H H H N H H H
    1-313 cyclopropyl CH2CH3 4-F H H CF3 N H H H
    1-314 cyclopropyl CH2CH3 2-F 4-F H CF3 N H H H
    1-315 cyclopropyl CH2CH3 4-F H H H N H H Cl
    1-316 cyclopropyl CH2CH3 4-Cl H H H N H H Cl
    1-317 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00074
         		H H H N H H H
    1-318 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00075
         		H H H N H H H
    1-319 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00076
         		H H H N H H H
    1-320 cyclopropyl CH2CH3 4-F H H H CH H H CH3
    1-321 cyclopropyl CH2CH3 4-CN H H H CH H H Cl
    1-322 cyclopropyl CH2CH3 4-F H H H N H F H
    1-323 cyclopropyl CH2CH3 4-F H H H N H Cl H
    1-324 cyclopropyl CH2CF3 4-F H H CF3 N H H H
    1-325 cyclopropyl CH2CF3 4-F H H Cl N H H H
    1-326 cyclopropyl CH2CH3 4-F H H Cl N H H H
    1-327 cyclopropyl CH3 4-Cl H H H C—Cl H H CH3
    1-328 cyclopropyl CH3 4-F H H H C—Cl H H CH3
    1-329 cyclopropyl CH3 4-F H H H CH Br H CH3
    1-330 cyclopropyl CH3 4-Cl H H H CH H Cl CH3
    1-331 cyclopropyl CH2CH3 4-Cl H H H C—CN H H H
    1-332 cyclopropyl CH2CH3 2-F 4-F H H C—CN H H H
  • TABLE 2
    Physiochemical characterization
    Ex. No. MH+ logP (HCOOH) NMR (400 MHz, DMSO-d6, unless indicated otherwise)
    1-1 364.2 0.71 (MeOH d4); 0.68 (2H, m), 0.90 (2H, m), 2.38 (3H, s), 2.94 (1H, m), 7.22 (2H, t), 7.35 (1H, m), 7.61 (2H, m),
    7.95 (1H, m), 8.49 (1H, m), 8.59 (1H, s).
    1-2 538.1 2.31
    1-3 538.1 2.27
    1-4 396.2 1.34
    1-5 396.0 0.56 (2H, m), 0.78 (2H, m), 1.06 (3H, t), 2.90 (1H, m), 6.88 (1H, s), 7.11 (1H, m), 7.22 (2H, m), 7.50 (1H, m),
    7.74 (1H, m), 8.52 (2H, m), 9.36 (1H, s).
    1-8 374.2
    1-9 396.1
    1-10 406.1
    1-11 378.1
    1-12 404.1
    1-13 394.1
    1-14 361.1 (MeCN d3); 0.56 (2H, m), 0.80 (2H, m), 1.13 (3H, t), 2.67 (2H, q), 2.89 (1H, m), 6.12 (1H, m), 7.22 (1H, m),
    7.41 (1H, m), 7.69 (1H, m), 7.97 (1H, m), 8.08 (1H, s), 8.58 (3H, m), 8.81 (1H, m).
    1-72 429.2 2.35
    1-73 430.0 1.45 0.60 (m, 2H), 0.78 (m, 2H), 2.24 (s, 3H), 2.91 (m, 1H), 7.29 (m, 1H), 7.39 (d, 2H), 7.76 (d, 2H), 7.95 (d, 1H),
    8.49 (m, 1H), 8.56 (m, 1H), 9.56 (s, 1H).
    1-74 432.1 1.55 1.26 (d, 6H), 2.36 (s, 3H), 4.41 (m, 1H), 5.75 (m, 1H), 7.31 (m, 1H), 7.40 (m, 2H), 7.78 (m, 2H), 7.99 (m, 1H),
    8.01 (m, 1H), 8.49 (m, 1H).
    1-75 450.1 1.99 0.78 (m, 2H), 0.89 (m, 2H), 3.15 (m, 1H), 7.34 (m, 3H), 7.76 (m, 2H), 7.95 (m, 1H), 8.40 (m, 1H), 8.60 (m, 1H),
    9.42 (m, 1H)
    1-76 452.1 2.05 1.27 (d, 6H), 4.40 (m, 1H), 7.13 (m, 1H), 7.48 (m, 3H), 7.77 (m, 2H), 7.90 (m, 1H), 8.48 (m, 1H), 8.64 (m, 1H),
    10.02 (m, 1H)
    1-78 451.1 2.55 1.20 (d, 6H), 4.38 (m, 1H), 6.85 (m, 1H), 7.28 (d, 2H), 7.53 (d, 2H), 7.73 (d, 2H), 7.84 (d, 2H), 8.48 (s, 1H),
    9.56 (s, 1H).
    1-80 433.1 2.33 0.61 (m, 2H), 0.77 (m, 2H), 2.93 (m, 1H), 6.66 (m, 1H), 7.40 (m, 2H), 7.46 (m, 2H), 7.78 (m, 2H), 7.84 (m, 2H),
    8.54 (s, 1H), 9.60 (s, 1H).
    1-81 413.1 2.33 0.58 (m, 2H), 0.77 (m, 2H), 2.07 (s, 3H), 2.91 (m, 1H), 6.97 (m, 1H), 7.22 (m, 2H), 7.48 (m, 2H), 7.73 (m, 2H),
    7.83 (m, 2H), 8.55 (s, 1H), 9.24 (s, 1H).
    1-82 434.0 1.94 0.54 (m, 2H), 0.80 (m, 2H), 2.91 (m, 1H), 6.81 (m, 1H), 7.50 (m, 1H), 7.78 (d, 2H), 7.99 (d, 1H), 8.06 (m, 1H),
    8.46 (m, 1H), 8.56 (m, 1H), 8.57 (m, 1H), 9.72 (s, 1H).
    1-83 414.1 1.43 0.58 (m, 2H), 0.77 (m, 2H), 2.21 (s, 3H), 2.90 (m, 1H), 7.14 (m, 1H), 7.28 (m, 1H), 7.76 (d, 2H), 7.84 (d, 2H),
    8.11 (m, 1H), 8.47 (m, 1H), 8.54 (m, 1H), 9.45 (s, 1H).
    1-84 468.1 2.19
    1-85 442.1 2.02 0.57 (m, 2H), 0.78 (m, 2H), 1.01 (d, 6H), 2.89 (m, 1H), 7.05 (m, 1H), 7.23 (m, 1H), 7.76 (d, 2H), 7.83 (d, 2H),
    7.85 (d, 2H), 8.54 (s, 1H), 9.70 (s, 1H).
    1-86 427.1 2.68 0.55 (m, 2H), 0.78 (m, 2H), 0.91 (t, 3H), 2.38 (q, 2H), 2.91 (m, 1H), 6.85 (m, 1H), 7.24 (m, 1H), 7.36 (m, 1H),
    7.45 (m, 1H) 7.76 (m, 3H), 7.84 (m, 2H), 8.55 (s, 1H), 9.28 (s, 1H).
    1-87 428.2 1.27
    1-88 447.0 1.93 0.53 (m, 2H), 0.73 (m, 2H), 2.34 (s, 3H), 2.94 (m, 1H), 6.43 (m, 1H), 7.44 (m, 4H), 7.72 (m, 4H), 9.51 (s, 1H)
    1-89 455.1 1.72 0.62 (m, 2H), 0.78 (m, 2H), 1.07 (m, 2H), 1.15 (m, 2H), 1.25 (m, 1H), 2.21 (s, 3H), 2.95 (m, 1H), 7.33 (m, 1H),
    7.80 (m, 5H), 7.86 (m, 1H), 8.49 (m, 1H), 9.70 (s, 1H).
    1-99 478.0 2.44 0.31 (m, 1H), 0.36 (m, 1H), 0.45 (, 1H), 0.50 (m, 1H), 1.00 (m, 1H), 1.20 (d, 3H), 3.76 (m, 1H), 5.81 (m, 1H),
    7.39 (m, 3H), 7.70 (m, 3H), 8.24 (s, 1H), 8.45 (s, 2H).
    1-100 458.1 1.80 0.31 (m, 1H), 0.36 (m, 1H), 0.45 (m, 1H), 0.50 (m, 1H), 1.10 (m, 1H), 1.28 (d, 3H), 3.80 (m, 1H), 6.59 (m, 1H),
    7.30 (m, 2H), 7.41 (m, 2H), 7.79 (m, 2H), 8.44 (s, 1H), 8.50 (s, 1H), 9.49 (s, 1H).
    1-111 504.1 2.65 0.36 (m, 4H), 0.50 (m, 4H), 1.11 (m, 2H), 3.56 (m, 1H), 6.21 (m, 1H), 7.44 (m, 2H), 7.53 (m, 2H), 7.79 (m, 2H),
    8.42 (s, 1H), 8.50 (s, 1H), 9.91 (s, 1H).
    1-112 415.2 2.12
    1-113 449.0 2.41 0.55 (m, 2H), 0.88 (m, 2H), 2.96 (m, 1H), 5.87 (m, 1H), 7.33 (m, 3H), 7.45 (m, 3H), 7.70 (m, 1H), 7.98 (m, 1H),
    8.40 (m, 1H), 8.56 (m, 1H)
    1-114 460 1.4 0.56 (2H, m), 0.78 (2H, m), 1.04 (3H, t), 2.91 (1H, m), 7.00 (1H, m), 7.26 (1H, m), 7.74 (4H, m), 7.85 (1H, 9),
    8.54 (2H, m), 9.42 (1H, s).
    1-115 419 1.40 0.55 (2H, m), 0.77 (2H, m), 1.04 (3H, t), 2.55 (2H, q), 2.89 (1H, m), 6.74 (1H, d), 6.96 (1H, m), 7.28 (1H, m),
    7.92 (2H, m), 8.44 (1H, m), 8.55 (2H, m), 9.41 (1H, s).
    1-116 446 1.81 0.58 (2H, m), 0.79 (2H, m), 2.23 (3H, s), 2.90 (1H, m), 7.10 (1H, s), 7.25 (1H, m), 7.75 (4H, m), 7.85 (1H, m),
    8.48 (1H, m), 8.54 (1H, s), 9.41 (1H, s).
    1-117 477 1.65
    1-119 485 1.80 0.55 (2H, m), 0.76 (2H, m), 2.32 (3H, s), 2.88 (1H, m), 5.13 (2H, s), 6.87 (1H, m), 7.01 (2H, d), 7.25 (1H, m),
    7.42 (4H, m), 7.64 (2H, d), 7.88 (1H, m), 8.49 (1H, m), 9.34 (1H, s).
    1-120 444 1.52
    1-121 467 1.15
    1-122 450 1.95 0.58 (2H, m), 0.78 (2H, m), 2.91 (1H, m), 7.33 (2H, m), 7.61 (2H, m), 7.95 (1H, m), 8.52 (1H, m), 8.57 (1H, s),
    9.41 (1H, s).
    1-123 512 1.79 0.58 (2H, m), 0.77 (2H, m), 2.25 (3H, s), 6.33 (1H, m), 7.04 (1H, m), 7.29 (3H, m), 7.74 (2H, m), 7.90 (1H, m),
    8.48 (1H, m), 8.83 (1H, s), 9.39 (1H, s).
    1-124 378 1.03
    1-126 329 1.60 0.57 (2H, m), 0.79 (2H, m), 1.03 (3H, t), 2.91 (1H, m), 6.86 (1H, m), 7.263 (1H, m), 7.44 (2H, m), 7.61 (1H, m),
    7.72 (1H, m), 8.50 (2H, m), 9.33 (1H, s).
    1-127 360 1.01 0.55 (2H, m), 0.76 (2H, m), 1.06 (3H, t), 2.55 (2H, q), 2.89 (1H, m), 6.86 (1H, m), 7.25 (1H, m), 7.37 (3H, m),
    7.62 (2H, m), 7.84 (1H, m), 8.52 (2H, m), 9.38 (1H, s).
    1-128 332 0.63 0.56 (2H, m), 0.73 (2H, m), 2.86 (1H, m), 7.17 (1H, s), 7.30 (3H, m), 7.46 (1H, m), 7.62 (2H, m), 8.10 (1H, m),
    8.52 (1H, s), 8.67 (1H, m), 8.96 (1H, m), 9.65 (1H, s).
    1-129 384 1.27 0.54 (2H, m), 0.79 (2H, m), 2.90 (1H, m), 6.64 (1H, m), 7.23 (2H, m), 7.51 (1H, m), 7.70 (2H, m), 7.94 (1H, m),
    8.47 (1H, m), 8.53 (1H, s), 9.69 (1H, s).
    1-130 401 1.55 0.61 (2H, m), 0.85 (2H, m), 3.00 (1H, m), 7.47 (1H, m), 7.53 (2H, m), 7.69 (2H, m), 8.02 (1H, m), 8.48 (1H, m),
    8.65 (1H, s)
    1-133 385.2 1.10 0.56 (2H, m), 0.78 (2H, m), 1.04 (3H, t), 2.89 (1H, m), 7.07 (1H, m), 7.27 (1H, m), 7.84 (6H, m), 8.55 (2H, m),
    9.40 (1H, s).
    1-134 394.2 1.53 1.34 (3H, t), 1.48 (9H, s), 2.67 (2H, q), 5.78 (1H, s), 7.29 (3H, m), 7.60 (1H, m), 7.68 (2H, m), 8.48 (1H, s),
    8.56 (1H, m), 9.61 (1H, s).
    1-135 410.1 1.86 1.31 (3H, t), 1.48 (9H, s), 2.65 (1H, s), 5.81 (1H, s), 7.30 (1H, m), 7.50 (2H, m), 7.64 (3H, m), 8.48 (1H, s),
    8.55 (1H, s), 9.61 (1H, s).
    1-136 401.2 1.81 1.11 (3H, t), 1.48 (9H, s), 2.61 (2H, q), 5.93 (1H, s), 7.30 (1H, m), 7.61 (1H, m), 7.81 (2H, d), 7.88 (2H, d),
    8.51 (1H, s), 8.55 (1H, m), 9.64 (1H, s).
    1-137 444.2 2.34 1.08 (3H, t), 1.49 (9H, s), 2.57 (2H, q), 5.88 (1H, s), 7.30 (1H, m), 7.61 (1H, m), 7.82 (4H, m), 8.51 (1H, s),
    8.54 (1H, s), 9.65 (1H, s).
    1-138 460.2 2.32 1.11 (2H, q), 1.48 (9H, s), 2.63 (2H, q), 5.82 (1H, s), 7.29 (1H, m), 7.39 (2H, m), 7.58 (1H, m), 7.75 (2H, m),
    8.49 (1H, s), 8.55 (1H, m), 9.63 (1H, s).
    1-139 412.1 0.79 0.56 (2H, m), 0.78 (2H, m), 1.04 (3H, t), 2.90 (1H, m), 6.82 (1H, m), 7.23 (2H, m), 7.44 (2H, m), 7.67 (1H, m),
    8.50 (2H, m), 9.30 (1H, m).
    1-140 394.1 1.07 1.19 (2H, m) 0.78 (2H, m), 1.03 (3H, t), 2.91 (1H, m), 6.80 (1H, m), 7.37 (1H, m), 7.37 (3H, m), 7.49 (1H, m),
    7.62 (1H, m), 8.48 (1H, m), 8.53 (1H, m), 9.28 (1H, m).
    1-141 395.2 1.65 1.12 (3H, t), 1.48 (9H, s), 2.66 (2H, q), 5.97 (1H, s), 7.24 (1H, m), 7.30 (1H, m), 7.62 (1H, m), 8.20 (1H, m),
    8.50 (2H, m), 8.55 (1H, m), 9.64 (1H, s).
    1-142 444.1 1.89 1.08 (3H, t), 1.48 (9H, m), 5.84 (1H, s), 7.26 (1H, m), 7.42 (3H, m), 7.64 (1H, m), 8.48 (1H, s), 8.52 (1H, m),
    9.56 (1H, s).
    1-143 406.2 1.47 0.41 (4H, m), 1.03 (1H, m), 1.12 (3H, t), 1.25 (3H, d), 2.67 (2H, q), 3.79 (1H, m), 6.40 (1H, d), 7.23 (2H, t),
    7.29 (2H, m), 7.72 (3H, m), 8.42 (1H, s), 8.55 (1H, m), 9.48 (1H, s).
    1-144 422.1 1.62 0.45 (4H, m), 1.05 (1H, m), 1.13 (3H, t), 1.24 (3H, d), 2.65 (2H, q), 3.77 (1H, m), 6.43 (1H, d), 7.30 (1H, m),
    7.48 (2H, d), 7.67 (2H, d), 7.76 (1H, d), 8.42 (1H, s), 8.56 (1H, d), 9.49 (1H, s).
    1-145 413.2 1.67 0.40 (4H, m), 1.10 (4H, m), 1.24 (3H, d), 2.61 (2H, q), 3.79 (1H, m), 6.59 (1H, d), 7.31 (1H, m), 7.76 (1H, m),
    7.84 (4H, m), 8.45 (1H, s), 8.56 (1H, m), 9.51 (1H, s).
    1-146 472.2 2.18 0.47 (4H, m) 1.09 (3H, t), 1.26 (3H, d), 2.62 (2H, q), 3.79 (1H, m), 6.45 (1H, d), 7.29 (1H, m), 7.40 (2H, d),
    7.76 (3H, m), 8.43 (1H, s), 8.55 (1H, m), 9.51 (1H, s).
    1-147 441.1 1.95 1.13 (4H, m), 1.35 (3H, d), 2.71 (2H, q), 4.25 (1H, m), 6.26 (1H, d), 7.26 (3H, m), 7.63 (1H, m), 7.72 (2H, m),
    8.48 (1H, s), 8.55 (1H, m), 9.68 (1H, s).
    1-148 490.1 2.67 1.09 (4H, m), 1.37 (2H, d), 2.59 (1H, m), 4.22 (1H, m), 6.25 (1H, d), 7.27 (1H, m), 7.44 (1H, m), 7.50 (2H, m),
    7.66 (1H, m), 8.50 (1H, s), 8.54 (1H, m), 9.67 (1H, s).
    1-149 458.1 2.26 1.16 (4H, m); 1.35 (3H, d), 2.70 (2H, q), 4.25 (1H, m) 6.30 (1H, m), 7.32 (1H, m), 7.51 (2H, d), 7.68 (3H, m),
    8.49 (1H, s), 8.56 (1H, m), 9.69 (1H, s).
    1-150 449.1 2.08 1.19 (4H, m), 1.35 (3H, d), 2.66 (1H, m), 4.3 (1H, m), 6.43 (1H, d), 7.32 (1H, m), 7.69 (4H, m), 8.52 (1H, s),
    8.57 (1H, m), 9.71 (1H, s).
    1-151 436.2 2.22 0.41 (6H, m), 1.13 (3H, t), 1.37 (4H, m), 1.50 (1H, m), 2.69 (2H, q), 5.73 (1H, s), 7.30 (1H, m), 7.50 (2H, s),
    7.57 (1H, d), 7.63 (2H, d), 8.47 (1H, s), 8.55 (1H, m), 9.73 (1H, s).
    1-152 386.2 1.32
    1-154 396.1 1.83 0.54 (2H, m), 0.75 (2H, m), 2.87 (1H, m), 3.99 (3H, s), 6.86 (1H, s), 7.10 (1H, m), 7.42 (2H, d), 7.70 (2H, d),
    8.01 (1H, m), 8.30 (1H, m), 8.52 (1H, s), 9.37 (1H, s).
    1-155 360.2 1.49 0.54 (2H, m); 0.75 (2H, m), 2.88 (1H, m), 3.99 (3H, s), 6.81 (1H, s), 7.14 (1H, m), 7.16 (2H, t), 7.74 (2H, m),
    8.00 (1H, m), 8.29 (1H, m), 8.51 (1H, s), 9.37 (1H, s).
    1-156 387.3 1.59 0.55 (2H, m), 0.75 (2H, m), 2.87 (1H, m), 3.99 (3H, s), 6.96 (1H, m), 7.09 (1H, m), 7.81 (4H, m), 7.99 (1H, m),
    8.29 (1H, m), 8.55 (1H, m), 9.38 (1H, s).
    1-157 446.1 2.21 0.54 (2H, m), 0.75 (2H, m), 2.88 (1H, m), 3.97 (3H, s), 6.86 (1H, s), 7.08 (1H, m), 7.33 (2H, m), 7.79 (2H, m),
    7.99 (1H, m), 8.28 (1H, m), 8.53 (1H, s), 9.38 (1H, s).
    1-158 410.0 2.54 0.53 (2H, m), 0.75 (2H, m), 1.31 (3H, t), 2.87 (1H, m), 4.47 (2H, q), 6.83 (1H, s), 7.09 (1H, m), 7.40 (2H, d),
    7.69 (2H, d), 8.03 (1H, m), 8.28 (1H, m), 8.52 (1H, s), 9.28 (1H, s).
    1-159 394.2 1.84 0.53 (2H, m), 0.74 (2H, m), 1.30 (3H, t), 2.86 (1H, m), 4.49 (2H, q), 6.79 (1H, s), 7.07 (1H, m), 7.16 (2H, t),
    7.72 (2H, m), 8.01 (1H, m), 8.28 (1H, m), 8.51 (1H, s), 9.29 (1H, s).
    1-160 401.2 1.80 0.54 (2H, m), 0.77 (2H, m), 1.31 (3H, t), 2.89 (1H, m), 4.49 (2H, q), 6.95 (1H, s), 7.07 (1H, m), 7.81 (4H, m),
    8.01 (1H, m), 8.23 (1H, m), 8.55 (1H, s), 9.30 (1H, s).
    1-161 460.1 2.64 0.53 (2H, m), 0.75 (2H, m), 1.27 (3H, t), 2.88 (1H, m), 4.45 (2H, q), 6.83 (1H, s), 7.07 (1H, m), 7.33 (2H, m),
    7.77 (2H, m), 8.03 (1H, m), 8.27 (1H, m), 8.53 (1H, s), 9.30 (1H, s).
    1-162 424.1 2.31 0.53 (2H, m), 0.75 (2H, m), 1.28 (6H, d), 2.86 (1H, m), 5.40 (1H, m), 6.82 (1H, m), 7.08 (1H, m), 7.42 (2H, d),
    7.63 (2H, d), 8.06 (1H, m), 8.28 (1H, m), 8.52 (1H, s), 9.15 (1H, s).
    1-163 408.2 2.19 0.54 (2H, m), 0.76 (2H, m), 1.28 (6H, d), 2.86 (1H, m), 5.40 (1H, m), 6.78 (1H, s), 7.06 (1H, m), 7.17 (2H, t),
    7.67 (2H, m), 8.06 (1H, m), 8.28 (1H, m), 8.52 9.16 (1H, s).
    1-164 415.1 2.27 0.55 (2H, m), 0.75 (2H, m), 1.27 (6H, d), 2.87 (1H, m), 5.40 (1H, m), 6.93 (1H, m), 7.06 (1H, m), 7.80 (4H, m),
    8.02 (1H, m), 8.27 (1H, m), 8.55 (1H, s), 9.16 (1H, s).
    1-165 474.1 2.32 0.54 (2H, m), 0.75 (2H, m), 1.24 (6H, d), 2.86 (1H, m), 5.39 (1H, m), 6.82 (1H, m), 7.07 (1H, m), 7.34 (2H, m),
    7.73 (2H, m), 8.05 (1H, m), 8.28 (1H, m), 8.53 (1H, s), 9.18 (1H, s).
    1-166 464.1 2.48 0.52 (2H, m), 0.76 (2H, m), 2.86 (1H, m), 5.10 (2H, q), 6.78 (1H, s), 7.22 (1H, m), 7.38 (2H, d), 7.70 (2H, d),
    8.04 (1H, m), 8.32 (1H, m), 8.53 (1H, s), 9.26 (1H, s).
    1-167 448.1 2.12 0.52 (2H, m), 0.75 (2H, m), 2.86 (1H, m), 5.10 (2H, q), 6.72 (1H, m), 7.14 (2H, q), 7.21 (1H, m), 7.71 (2H, m),
    8.02 (1H, m), 8.31 (1H, m), 8.52 (1H, s), 9.26 (1H, s).
    1-168 455.2 2.11 0.53 (2H, m), 0.76 (2H, m), 2.89 (1H, m), 5.11 (2H, q), 6.89 (1H, m), 7.22 (2H, m), 7.83 (4H, m), 8.01 (1H, m),
    8.31 (1H, m), 8.56 (1H, s), 9.28 (1H, s).
    1-169 514.0 2.84 0.52 (2H, m), 0.75 (2H, m), 2.8 (1H, m), 5.11 (2H, q), 6.78 (1H, m), 7.21 (1H, m), 7.31 (2H, m), 7.77 (2H, m),
    8.03 (1H, m), 8.32 (1H, m), 8.54 (1H, s), 9.28 (1H, s).
    1-170 418.3 1.59 0.50 (2H, m), 0.79 (3H, m), 2.91 (1H, m), 6.50 (1H, m), 7.26 (2H, t), 7.33 (2H, m), 7.93 (1H, m), 8.54 (1H, s),
    8.80 (1H, m), 9.72 (1H, s).
    1-177 394.1 1.31 0.55 (2H, m), 0.78 (2H, m), 1.063 (3H, t), 2.89 (1H, m), 6.94 (1H, s), 7.28 (1H, m), 7.45 (2H, d), 7.67 (2H, d),
    7.88 (1H, d), 8.52 (2H, m), 9.37 (1H, s).
    1-178 434.2 1.76 0.49 (2H, m), 0.80 (2H, m), 2.93 (1H, m), 6.56 (1H, m), 7.51 (2H, m), 7.70 (2H, m), 7.82 (1H, m), 7.96 (1H, m),
    8.54 (1H, s), 8.81 (1H, m), 9.7 (1H, s).
    1-179 416.1 1.58
    1-180 390.1 1.10 0.57 (2H, m), 0.78 (2H, m), 1.02 (3H, t), 2.20 (3H, s), 2.42 (2H, q), 2.89 (1H, m), 6.82 (1H, s), 6.96 (1H, m),
    7.07 (1H, m), 7.20 (2H, m), 7.68 (1H, m), 8.50 (2H, m), 9.21 (1H, s).
    1-181 397.2 1.22 0.58 (2H, m), 0.79 (2H, m), 1.00 (3H, t), 2.25 (3H, s), 2.38 (2H, q), 2.90 (1H, m), 6.97 (1H, m), 7.21 (1H, m),
    7.38 (1H, m), 7.61 (1H, m), 7.71 (3H, m), 8.49 (1H, m), 8.52 (1H, s), 9.28 (1H, s).
    1-182 374.2 0.94
    1-183 393.1 0.94
    1-184 (MeOH d4); (0.66 (2H, m), 0.89 (2H, m), 1.10 (3H, t), 2.21 (3H, s), 2.50 (2H, q), 2.88 (1H, m), 7.01 (1H, m),
    7.07 (1H, m), 7.27 (1H, m), 7.32 (1H, m), 7.72 (1H, d), 8.49 (1H, m), 8.53 (1H, s).
    1-185 (MeOH d4); 0.63 (2H, m), 0.89 (2H, m), 1.10 (3H, t), 2.55 (2H, q), 7.30 (1H, m), 7.36 (2H, d), 7.68 (2H, d),
    7.91 (1H, m), 8.52 (2H, m).
    1-186 (MeOH d4); 0.65 (2H, m); 0.89 (2H, m), 1.06 (3H, t), 2.49 (2H, q), 2.86 (1H, m), 7.31 (1H, m), 7.76 (4H, s),
    7.94 (1H, m), 8.52 (1H, m), 8.56 (1H, s).
    1-187 412.1 1.46 0.56 (2H, m), 0.78 (2H, m), 1.05 (3H, t), 2.89 (1H, m), 6.90 (1H, s), 7.25 (1H, m), 7.33 (1H, m), 7.44 (2H, m),
    7.76 (1H, m), 8.5 (2H, m), 9.38 (1H, s).
    1-188 408.2 1.40 0.58 (2H, m), 0.78 (2H, m), 1.02 (3H, t), 2.20 (3H, s), 2.90 (1H, m), 6.86 (1H, m), 7.20 (3H, m), 7.32 (1H, m),
    7.73 (1H, m), 8.50 (2H, m), 9.23 (1H, s).
    1-189 442.0 1.77 0.59 (2H, m), 0.78 (2H, m), 0.95 (3H, t), 2.28 (3H, s), 2.91 (1H, m), 6.93 (1H, m), 7.19 (1H, m), 7.40 (1H, m),
    7.51 (1H, m), 7.60 (1H, m), 7.73 (1H, m), 8.47 (1H, m), 8.53 (1H, s), 9.28 (1H, s).
    1-196 446.2 2.43 0.56 (2H, m), 0.79 (2H, m), 1.07 (2H, q), 2.89 (1H, m), 7.04 (1H, m), 7.20 (2H, t), 7.68 (2H, m), 7.80 (1H, d),
    8.18 (1H, d), 8.53 (1H, s), 9.56 (1H, s).
    1-197 440.1 2.52 0.58 (2H, m); 0.76 (4H, m), 0.86 (2H, m), 1.77 (1H, m); 2.86 (1H, m), 7.18 (1H, m), 7.42 (2H, d), 7.58 (2H, d),
    8.14 (1H, m), 8.46 (1H, m), 8.52 (1H, s), 9.62 (1H, s).
    1-198 424.1 2.16 0.58 (2H, m), 0.73 (2H, m), 0.79 (2H, m), 0.86 (2H, m), 1.83 (1H, m), 2.87 (1H, m), 7.20 (3H, m), 7.61 (2H, m),
    8.11 (1H, m), 8.45 (1H, m), 8.51 (1H, s), 9.61 (1H, s).
    1-199 448.1 2.35 0.57 (2H, m), 1.12 (2H, m), 2.47 (3H, s), (2.89 (1H, m), 7.15 (1H, s), 7.47 (2H, d), 7.65 (2H, d), 7.82 (1H, d),
    8.16 (1H, d), 8.53 (1H, s), 9.57 (1H, s).
    1-224 392.1 1.36
    1-229 408.1 1.58
    1-230 426.1 1.72
    1-254 450.1 1.83
    1-258 577.3 2.07
    1-262 433 1.45 (d7-DMF): 0.87 (8H, m), 3.03 (1H, m), 3.18 (1H, m), 7.39 (2H, t), 7.70 (m, 1H), 7.80 (3H, m), 8.19 (1H, d),
    8.55 (1H, s), 8.68 (1H, dd), 9.11 (1H, bd), 9.72 (1H, bd)
    1-263 417 2.20 0.48 (2H, m), 0.84 (2H, m), 2.95 (1H, m), 6.01 (1H, bs), 7.35 (2H, m), 7.47 (3H, m), 7.68 (2H, m), 8.57 (1H, s),
    10.06 (1H, s)
    1-264 591.2 1.9
    1-273 509.2 1.11
    1-275 374 0.76 0.55 (2 H, m), 0.76 (2 H, m), 1.05 (3 H, t), 2.53 (2 H, q), 2.92 (1 H, m), 6.63 (1 H, m), 7.24 (1 H, m),
    7.38 (3 H, m), 7.60 (2 H, m), 7.80 (1 H, m), 8.51 (1 H, m), 9.27 (1 H, m).
    1-276 392 0.88 0.55 (2 H, m), 0.76 (2 H, m), 1.06 (3 H, t), 2.53 (2 H, q), 2.92 (1 H, m), 3.13 (3 H, s), 6.69 (1 H, m),
    7.20 (2 H, m), 7.25 (1 H, m), 7.65 (2 H, m), 7.83 (1 H, m), 8.52 (1 H, m), 9.28 (1 H, m).
    1-277 442/444 1.34 0.55 (2 H, m), 0.77 (2 H, m), 1.03 (3 H, t), 2.45 (2 H, q), 2.93 (1 H, m), 6.66 (1 H, m), 7.21 (1 H, m),
    7.43 (2 H, m), 7.60 (1 H, m), 7.68 (1 H, m), 8.49 (1 H, m), 9.22 (1 H, m).
    1-278 410 1 0.55 (2 H, m), 0.77 (2 H, m), 1.05 (3 H, t), 2.47 (3 H, s), 2.50 (2 H, q), 2.93 (1 H, m), 6.66 (1 H, m),
    7.10 (1 H, m), 7.21 (2 H, m), 7.47 (1 H, m), 7.71 (1 H, m), 8.50 (1 H, m), 9.25 (1 H, m).
    1-279 458 1.44 0.55 (2 H, m), 0.76 (2 H, m), 1.03 (3 H, t), 2.92 (1 H, m), 6.75 (1 H, m), 7.24 (1 H, m), 7.35 (2 H, m),
    7.73 (2 H, m), 7.85 (1 H, m), 8.52 (1 H, m), 9.31 (1 H, m).
    1-287 521.2 1.45
    1-290 605.2 2.47
    1-299 433.1 1.85 1.17 (3H, CH3), 1.40 (3H, CH3, s), 2.75 (2H, CH2), 5.23 (1H, m), 6.08 (1H, d), 7.20 (3H, m), 7.66 (3H, m),
    8.14 (1H, s), 8.55 (2H, m)
    1-302 467 2.76 0.49 (2H, m), 0.80 (2H, m), 2.91 (1H, m), 6.48 (1H, m), 7.49 (2H, m), 7.57 (1H, d), 7.70 (2H, m), 7.87 (2H, m),
    8.54 (1H, s), 9.65 (1H, bs)
    1-303 397 2.16 0.56 (2H, m), 0.76 (2H, m), 2.11 (3H, s), 2.88 (1H, m), 6.94 (1H, m), 7.19 (2H, m), 7.30 (2H, m), 7.54 (1H, d),
    7.67 (2H, m), 8.50 (1H, s) 9.26 (1H, bs)
    1-304 413 2.44 0.56 (2H, m), 0.76 (2H, m), 2.11 (3H, s), 2.88 (1H, m), 6.97 (1H, m), 7.31 (2H, m), 7.44 (2H, m), 7.55 (1H, d),
    7.66 (2H, m), 8.51 (1H, s), 9.27 (1H, bs)
    1-305 589.1 2.04
    1-306 535.1 1.84
    1-308 450 1.83 0.55 (2 H, m), 0.77 (2 H, m), 2.88 (1 H, m), 6.13 (1 H, dq), 7.18 (3 H, m), 7.67 (3 H, m), 8.23 (1 H, m),
    8.54 (1 H, m), 8.80 (1 H, m), 8.89 (1 H, m).
    1-309 535.2 1.77
    1-310 555.1 1.84
    1-315 411 2.18 (d3-MeCN): 0.53 (2H, m), 0.83 (2H, m), 0.92 (3H, t), 2.02 (2H, q), 2.95 (1H, m), 6.03 (1H, m), 7.19 (3H, m),
    7.31 (2H, m), 7.55 (2H, m), 8.11 (1H, bs), 8.55 (1H, s)
    1-316 427 2.54 (d3-MeCN): 0.53 (2H, m), 0.83 (2H, m), 0.93 (3H, t), 2.01 (2H, q), 2.94 (1H, m), 6.03 (1H, bs), 7.20 (1H, m),
    7.30 (2H, m), 7.48 (3H, m), 7.63 (1H, m), 8.09 (1H, bs), 8.56 (1H, s)
    1-320 391 2.39 0.47 (2H, m), 0.82 (2H, m), 0.98 (3H, t), 2.03 (3H, s), 2.20 (2H, q), 2.91 (1H, m), 6.48 (1H, m), 7.03 (2H, m),
    7.25 (3H, m), 7.61 (2H, dd), 8.53 (1H, s), 9.45 (1H, bs)
    1-321 418 2.37 0.47 (2H, m), 0.85 (5H, m), 1.97 (2H, q), 2.93 (1H, m), 6.42 (1H, m), 7.24 (1H, m), 7.36 (2H, m), 7.55 (2H, d),
    7.72 (2H, d), 8.59 (1H, s), 9.93 (1H, s)
    1-327 413 2.42 0.57 (2H, m), 0.77 (2H, m), 1.96 (3H, s), 2.84 (1H, m), 7.22 (1H, m), 7.42 (4H, m), 7.62 (2H, m), 7.73 (1H, m),
    8.52 (1H, s), 9.50 (1H, bs)
    1-328 397 2.07 0.57 (2H, m), 0.77 (2H, m), 1.96 (3H, s), 2.84 (1H, m), 7.22 (3H, m), 7.38 (2H, m), 7.65 (2H, m), 7.73 (1H, m),
    8.52 (1H, s), 9.49 (1H, bs)
    1-329 441, 443 2.17 0.56 (2H, m), 0.76 (2H, m), 2.05 (3H, s), 2.84 (1H, m), 7.24 (3H, m), 7.46 (2H, m), 7.55 (1H, d), 7.67 (2H, dd),
    8.51 (1H, s), 9.38 (1H, bs)
    1-330 413 2.39 0.55 (2H, m), 0.78 (2H, m), 2.04 (3H, s), 2.86 (1H, m), 7.29 (2H, m), 7.50 (4H, m), 7.66 (2H, m), 8.54 (1H, s),
    9.44 (1H, bs)
  • TABLE 3
    Compounds of the formula
    Figure US20120071496A1-20120322-C00077
    Ex.
    No. R1 R5 R7 R6 A G4 G5 G6
    3-1 cyclopropyl Cl CH2CH3 H N H H H
    3-2 cyclopropyl H CH2CH3 H N H H H
    3-3 cyclopropyl Br CH2CH3 H N H H H
    3-4 cyclopropyl Cl OCH2CF3 H N H H H
    3-5 cyclopropyl Cl CH2CF3 H N H H H
    3-6 cyclobutyl Cl CH2CH3 H N H H H
    3-7
    Figure US20120071496A1-20120322-C00078
         		Cl CH2CH3 H N H H H
    3-8 cyclopropyl CH2CH3 CH2CH3 H N H H H
    3-9 cyclopropyl Cl CH2CH3 CH3 N H H H
     3-10 CH(CF3)CH3 Cl CH2CH3 CH3 N H H H
     3-11 cyclopropyl Cl CH2CH3 CF3 N H H H
     3-12
    Figure US20120071496A1-20120322-C00079
         		Cl CH2CH3 H N H H H
     3-13 cyclopropyl cyclo- CH2CF3 Cl N H H H
    propyl
     3-14
    Figure US20120071496A1-20120322-C00080
         		Cl CH2CH3 CH3 N H H H
     3-15
    Figure US20120071496A1-20120322-C00081
         		Cl CH2CH3 H N H H H
     3-16
    Figure US20120071496A1-20120322-C00082
         		Cl CH2CH3 H N H H H
  • TABLE 4
    Physicochemical characterization
    Ex. No. MH+ logP (HCOOH)
    3-1 318.2 0.79
    3-3 364.1 0.84
    3-4 388.0 2.25
    3-5 370.1 1.61
    3-6 331.1 1.34
    3-7 331.1 1.26
    3-8 312.2 1.74
    3-9 332.2 1.41
    3-10 374.0 1.65
    3-11 384.1 2.27
    3-12 412.1 2.22
  • TABLE 5
    Compounds of the formula
    Figure US20120071496A1-20120322-C00083
    Ex. No. G1 G2 G3 R5 R7 R6 A G4 G5 G6
    5-1 4-Cl H H Cl CH2CH3 H N H H H
    5-2 4-F H H Cl CH2CH3 H N H H H
    5-3 2-CH3
    Figure US20120071496A1-20120322-C00084
         		H Cl CH2CH3 H N H H H
    5-4 2-CH3 4-C3F7 H Cl CH2CH3 H N H H H
    5-5 4-CF3 H H Cl CH2CH3 H N H H H
    5-6 4-CN H H Cl CH2CH3 H N H H H
    5-7 2-CH3
    Figure US20120071496A1-20120322-C00085
         		H Cl CH2CH3 H N H H H
    5-8 2-F 4-F H Cl CH2CH3 H N H H H
    Figure US20120071496A1-20120322-C00086
  • TABLE 6
    Physicochemical characterization
    Ex. No. MH+ logP (HCOOH)
    5-1 388.1 1.75
    5-2 372.1 1.25
    5-3 635.1 3.20
    5-4 536.1 3.68
    5-5 422.1 2.12
    5-6 379.1 1.38
    5-7 585.1 2.62
    5-8 390.1 1.40
  • TABLE 7
    Compounds of the formula
    Figure US20120071496A1-20120322-C00087
    Ex. No. R1 R9 R10 R11 R5 G1 G2 G3 R6 A
    7-1 cyclopropyl CH2CH3 H H Ph 4-F H H H N
    7-2 cyclopropyl CH2CH3 H Cl Ph 4-F H H H N
    7-3 cyclopropyl CH2CH3 H H Ph H H H H N
    7-4 cyclopropyl CH2CH3 H H Ph 4-Cl H H H N
    7-5 cyclopropyl CH2CH3 H H Ph 4-OCF3 H H H N
    7-6 cyclopropyl CH2CH3 H H Ph 4-SCF3 H H H N
    7-7 cyclopropyl CH2CH3 H Cl Ph H H H H N
    7-8 cyclopropyl CH2CH3 H Cl Ph 4-Cl H H H N
    7-9 cyclopropyl CH2CH3 H Cl Ph 4-OCF3 H H H N
     7-10 cyclopropyl CH2CH3 H Cl Ph 4-SCF3 H H H N
     7-11 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00088
         		H Cl H H H H N
     7-12 cyclopropyl CH2CH3 H H Ph 4-CN H H H N
     7-13 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00089
         		H Ph H H H H N
     7-14 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00090
         		H Ph 2-Cl 4-Cl H H N
     7-15 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00091
         		H Ph 4-OCF3 H H H N
     7-16 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00092
         		H Ph 4-Cl H H H N
     7-17 cyclopropyl CH2CH3
    Figure US20120071496A1-20120322-C00093
         		H Ph 4-F H H H N
     7-18 cyclopropyl CH2CH3 H H Ph 2-Cl 4-Cl H H N
     7-19 cyclopropyl CH2CH3 H Cl Ph 2-Cl 4-Cl H H N
     7-20 cyclopropyl CH2CH3 H Cl Ph 4-CN H H H N
     7-21 cyclopropyl CH(CH3)2 H Cl Ph 4-F H H H N
     7-22 cyclopropyl CH(CH3)2 H Cl Ph 4-Cl H H H N
     7-23 cyclopropyl CH2CF3 H H Ph 4-F H H H N
     7-24 cyclopropyl n-propyl H Cl Ph 4-F H H H N
     7-25 cyclopropyl n-propyl H Cl Ph 4-Cl H H H N
    Figure US20120071496A1-20120322-C00094
  • TABLE 8
    Physicochemical characterization
    Ex. No. MH+ logP (HCOOH) NMR (DMSO d6. 400 MHz)
    7-1 367 1.31 0.52 (2 H, m), 0.77 (2 H, m), 1.22 (3 H, t), 2.91 (1 H, m), 4.12 (2 H, q), 6.86 (1 H, m), 7.18 (2 H, m),
    7.59 (1 H, s), 7.71 (2 H, m), 8.53 (1 H, s), 9.19 (1 H, s)
    7-2 401/403 1.86 0.51 (2 H, m), 0.77 (2 H, m), 1.21 (3 H, t), 2.87 (1 H, m), 4.14 (2 H, q), 7.23 (2 H, m), 7.26 (1 H, m),
    7.64 (1 H, s), 7.71 (2 H, m), 8.54 (1 H, s), 9.27 (1 H, s)
    7-3 349 1.12 0.56 (2 H, m), 0.73 (2 H, m), 1.18 (3 H, t), 2.87 (1 H, m), 4.30 (2 H, q), 6.84 (1 H, m), 7.12 (1H, m),
    7.33 (3 H, m), 7.43 (1 H, m), 7.63 (2 H, m), 8.51 (1 H, s), 9.36 (1 H, s)
    7-4 383/385 1.6 0.55 (2 H, m), 0.74 (2 H, m), 1.16 (3 H, t), 2.84 (1 H, m), 4.31 (2 H, q), 6.85 (1 H, m), 7.42 (2 H, m),
    7.48 (1 H, m), 7.65 (2 H, m), 8.52 (1 H, s), 9.55 (1 H, s)
    7-5 433 1.99 0.57 (2 H, m), 0.74 (2 H, m), 1.14 (3 H, t), 2.88 (1 H, m), 4.29 (2 H, q), 6.87 (1 H, m), 7.22 (1 H, m),
    7.30 (2 H, m), 7.44 (1 H, m), 7.75 (2 H, m), 8.52 (1 H, s), 9.39 (1 H, s)
    7-6 449 2.29 0.57 (2 H, m), 0.74 (2 H, m), 1.13 (3 H, t), 2.89 (1 H, m), 4.27 (2 H, q), 6.86 (1 H, m), 7.25 (1 H, m),
    7.44 (1 H, m), 7.66 (2 H, m), 7.76 (2 H, m), 8.53 (1 H, s), 9.41 (1 H, s)
    7-7 383 1.63 0.52 (2 H, m), 0.77 (2 H, m), 1.19 (3 H, t), 2.91 (1 H, m), 4.09 (2 H, q), 6.78 (1 H, m), 7.37 (3 H, m),
    7.58 (1 H, m), 7.65 (2 H, s), 8.54 (1 H, s), 9.21 (1 H, s)
    7-8 417/419 2.20 0.52 (2 H, m), 0.77 (2 H, m), 1.20 (3 H, t), 2.91 (1 H, m), 4.12 (2 H, q), 6.90 (1 H, m), 7.43 (2 H, m),
    7.59 (1 H, m), 7.64 (1 H, s), 7.68 (2 H, m), 8.54 (1 H, s), 9.20 (1 H, s)
    7-9 467/469 2.63 0.52 (2 H, m), 0.77 (2 H, m), 1.20 (3 H, t), 2.92 (1 H, m), 4.11 (2 H, q), 6.88 (1 H, m), 7.35 (2 H, m),
    7.58 (1 H, s), 7.75 (2 H, m), 8.55 (1 H, s), 9.24 (1, H, s)
    7-10 483/485 2.99 0.52 (2 H, m), 0.77 (2 H, m), 1.19 (3 H, t), 2.92 (1 H, m), 4.10 (2 H, q), 6.88 (1 H, m), 7.58 (1 H, s),
    7.74 (4 H, m), 8.56 (1 H, s), 9.25 (1 H, s)
    7-11 523/525 3.29 0.52 (2 H, m), 0.72 (2 H, m), 1.31 (3 H, t), 2.83 (1 H, m), 4.45 (2 H, q), 5.57 (2 H, s), 6.94 (1 H, m),
    7.49 (2 H, m), 8.27 (1 H, s), 9.57 (1 H, s)
    7-12 374 1.45 0.58 (2 H, m), 0.74 (2 H, m), 1.15 (3 H, t), 2.88 (1 H, m), 4.28 (2 H, q), 6.86 (1 H, m), 7.31 (1 H, m),
    7.45 (1 H, m), 7.79 (4 H, m), 8.54 (1 H, s), 9.40 (1 H, s)
    7-13 565 2.80 0.53 (2 H, m), 0.72 (2 H, m), 1.17 (3 H, t), 2.86 (1 H, m), 4.27 (2 H, q), 5.52 (2 H, s), 6.72 (1 H, m),
    7.18 (1 H, m), 7.30 (3 H, m), 7.51 (1 H, s), 7.60 (2 H, m), 8.50 (1 H, s), 9.41 (1 H, s)
    7-14 633/635 3.79 0.54 (2 H, m), 0.73 (2 H, m), 1.14 (3 H, t), 2.87 (1 H; m), 4.23 (2 H, q), 5.50 (2 H, s), 6.62 (1 H, m),
    7.21 (1 H, m), 7.28 (2 H, m), 7.49 (2 H, m), 8.49 (1 H, s), 9.29 (1 H, s)
    7-15 649 3.76 0.54 (2 H, m), 0.73 (2 H, m), 1.14 (3 H, t), 2.86 (1 H, m), 4.26 (2 H, q), 5.53 (2 H, s), 6.74 (1 H, m),
    7.26 (3 H, m), 7.50 (1 H, s), 7.71 (2 H, m), 8.50 (1 H, s), 9.43 (1 H, s)
    7-16 599/601 3.41 0.53 (2 H, m), 0.72 (2 H, m), 1.17 (3 H, t), 2.85 (1 H, m), 4.28 (2 H, q), 5.53 (2 H, s), 6.77 (1 H, m),
    7.26 (1 H, m), 7.35 (2 H, m), 7.50 (1 H, m), 7.60 (2 H, m), 8.50 (1 H, s), 9.42 (1 H, s)
    7-17 583 3.05 0.52 (2 H, m), 0.73 (2 H, m), 1.17 (3 H, t), 2.85 (1 H, m), 4.28 (2 H, q), 5.54 (2 H, s), 6.74 (1 H, m),
    7.11 (2 H, m), 7.23 (1 H, m), 7.51 (1 H, s), 7.66 (2 H, m), 8.49 (1 H, s), 9.41 (1 H, s)
    7-18 417/419 1.95 0.57 (2 H, m), 0.76 (2 H, m), 1.15 (3 H, t), 2.88 (1 H, m), 4.27 (2 H, q), 6.73 (1 H, m), 7.17 (1 H, m),
    7.3-7.6 (4 H, m), 8.59 (1 H, s), 9.25 (1 H, s)
    7-19 451/453 2.57
    7-20 408/410 1.90 0.53 (2 H, m), 0.76 (2 H, m), 1.20 (3 H, t), 2.91 (1 H, m), 4.11 (2 H, q), 7.03 (1 H, m), 7.58 (1 H, m),
    7.82 (4 H, m), 8.56 (1 H, s), 9.21 (1 H, s)
    7-21 415 2.18 0.49 (2H, m), 0.78 (2H, m), 1.27 (6H, d), 2.91 (1H, m), 4.55 (1H, m), 6.66 (1H, bs), 7.20 (2H, m),
    7.61 (1H, s), 7.70 (2H, m), 8.54 (1H, s), 9.36 (1H, bs)
    7-22 431 2.58 0.49 (2H, m), 0.78 (2H, m), 1.27 (6H, d), 2.92 (1H, m), 4.54 (1H, m), 6.69 (1H, bs), 7.44 (2H, m),
    7.61 (1H, s), 7.67 (2H, m) 8.54 (1H, s), 9.37 (1H, bs)
    7-23 421 1.68 0.54 (2H, m), 0.75 (2H, m), 2.86 (1H, m), 5.34 (2H, m), 7.09 (1H, s), 7.17 (2H, m), 7.39 (1H, s),
    7.68 (3H, m), 8.54 (1H, s), 9.76 (1H, bs)
    7-24 415 2.13 0.49 (2H, m), 0.75 (5H, m), 1.57 (2H, m), 2.88 (1H, m), 4.06 (t, 2H), 7.07 (1H, m), 7.22 (2H, m),
    7.64 (1H, m), 7.73 (2H, m), 8.54 (1H, s) 9.30 (1H, bs)
    7-25 431 2.51 0.49 (2H, m), 0.74 (5H, m), 1.57 (2H, m), 2.88 (1H, m), 4.05 (t, 2H), 7.10 (1H, m), 7.46 (2H, m),
    7.65 (1H, m), 7.69 (2H, m), 8.55 (1H, s), 9.31 (1H, bs)
  • TABLE 9
    Compounds of the formula
    Figure US20120071496A1-20120322-C00095
    Ex. No. R1 G4 G5 G6 R10 R11 G1 G2 G3 R6 A
    9-1 cyclopropyl 4-F H H H H 4-F H H H N
    9-2 cyclopropyl 4-Cl H H H H 4-F H H H N
    9-3 cyclopropyl 2-Cl H H H H 4-F H H H N
    9-4 cyclopropyl 2-Cl H H H H 4-Cl H H H N
    Figure US20120071496A1-20120322-C00096
    Figure US20120071496A1-20120322-C00097
  • Ex. No. MH+ IogP (HCOOH) NMR (DMSO d6, 400 MHz)
    9-1 433 1.70 0.57 (2H, m), 0.78 (2H, m), 2.87 (1H, m), 7.06 (1H, s), 7.20 (4H, m), 7.32 (2H, m), 7.51 (1H, m), 7.73 (3H, m),
    8.50 (1H, s), 9.69 (1H, bs)
    9-2 449 2.02 0.57 (2H, m), 0.77 (2H, m), 2.87 (1H, m), 7.07 (1H, s), 7.18 (2H, m), 7.31 (2H, m), 7.49 (3H, m), 7.66 (2H, m),
    7.76 (1H, s), 8.51 (1H, s), 9.70 (1H, bs)
    9-3 449 1.76 0.52 (2H, m), 0.73 (2H, m), 2.81 (1H, m), 7.18 (4H, m), 7.27 (1H, m), 7.35 (1H, m), 7.42 (1H, m), 7.49 (1H, m),
    7.67 (2H, m), 7.80 (1H, m), 8.48 (1H, s), 9.68 (1H, bs)
    9-4 465 2.05 0.53 (2H, m), 0.73 (2H, m), 2.81 (1H, m), 7.18 (1H, m), 7.24 (2H, m), 7.35 (1H, m), 7.44 (3H, m), 7.52 (1H, m),
    7.63 (2H, m), 7.81 (1H, m), 8.49 (1H, s), 9.68 (1H, bs)
    • BIOLOGICAL EXAMPLES Lucilia Cuprina Test
  • Solvent: dimethyl sulphoxide
  • To produce a suitable preparation of active compound, 10 mg of active compound are mixed with 0.5 ml of dimethyl sulphoxide, and the concentrate is diluted with water to the desired concentration.
  • Vessels containing horse meat treated with the active compound preparation of the desired concentration are populated with Lucilia cuprina larvae.
  • After 48 hours, the activity in % is determined. 100% means that all larvae have been killed; 0% means that none of the larvae has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 100 ppm:
  • Ex. Nos.: 1-1, 1-21, 1-4, 1-5, 1-73, 1-74, 1-75, 1-76, 1-82, 1-83, 1-85, 1-86, 1-88, 1-100, 1-111, 1-113, 1-114, 1-116, 1-123, 1-124, 1-126, 1-133, 1-177, 1-179, 1-180, 1-181, 1-185, 1-186, 1-187, 1-188, 1-190
    • Musca Domestica Test
  • Solvent: dimethyl sulphoxide
  • To produce a suitable preparation of active compound, 10 mg of active compound are mixed with 0.5 ml of dimethyl sulphoxide, and the concentrate is diluted with water to the desired concentration.
  • Vessels containing a sponge treated with the active compound preparation of the desired concentration are populated with adult Musca domestica.
  • After 2 days, the activity in % is determined. 100% means that all flies have been killed; 0% means that none of the flies has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 100 ppm:
  • Ex. Nos.: 1-1, 1-4, 1-73, 1-75, 1-88, 1-114, 1-124, 1-126, 1-177, 1-179, 1-180, 1-181, 1-185, 1-186, 1-187, 1-190
  • Boophilus microplus test (injection)
    Solvent: dimethyl sulphoxide
  • To produce a suitable preparation of active compound, 10 mg of active compound are mixed with 0.5 ml of solvent, and the concentrate is diluted with water to the desired concentration. The solution of active compound is injected into the abdomen (Boophilus microplus), the animals are trans-ferred into dishes and stored in a climatized room. Activity is assessed via oviposition of fertile eggs.
  • After 7 days, the activity in % is determined. 100% means that none of the ticks has laid any fertile eggs.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 20 μg/animal:
  • Ex. Nos.: 1-5, 1-100, 1-111, 1-177, 1-187
    • Myzus Test (Spray Treatment)
  • Solvents: 78 parts by weight of acetone
      • 1.5 parts by weight of dimethylformamide
        Emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of Chinese cabbage leaves (Brassica pekinensis) which are infested by all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration
  • After 6 days, the activity in % is determined. 100% means that all aphids have been killed; 0% means that none of the aphids has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 500 ppm:
  • Ex. Nos.: 1-1, 1-10, 1-11, 1-114, 1-115, 1-116, 1-121, 1-123, 1-124, 1-126, 1-127, 1-129, 1-13, 1-130, 1-131, 1-132, 1-133, 1-139, 1-145, 1-146, 1-147, 1-148, 1-149, 1-150, 1-152, 1-154, 1-16, 1-174, 1-175, 1-176, 1-177, 1-178, 1-179, 1-180, 1-181, 1-183, 1-184, 1-185, 1-186, 1-187, 1-188, 1-189, 1-19, 1-190, 1-20, 1-21, 1-26, 1-27, 1-22, 1-23, 1-24, 1-25, 1-29, 1-30, 1-31, 1-32, 1-33, 1-37, 1-38, 1-4, 1-40, 1-44, 1-48, 1-5, 1-52, 1-59, 1-60, 1-7, 1-70, 1-71, 1-8, 1-9, 1-100, 1-112, 1-73, 1-85, 1-99
    • Phaedon Test (Spray Treatment)
  • Solvents: 78 parts by weight of acetone
      • 1.5 parts by weight of dimethylformamide
        Emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of Chinese cabbage (Brassica pekinensis) are sprayed with an active compound preparation of the desired concentration and, after drying, populated with larvae of the mustard beetle (Phaedon cochleariae).
  • After 7 days, the activity in % is determined. 100% means that all beetle larvae have been killed; 0% means that none of the beetle larvae has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 500 ppm:
  • Ex. Nos.: 1-1, 1-11, 1-114, 1-115, 1-116, 1-119, 1-122, 1-123, 1-124, 1-126, 1-127, 1-129, 1-13, 1-130, 1-131, 1-132, 1-133, 1-134, 1-135, 1-136, 1-137, 1-139, 1-14, 1-140, 1-141, 1-142, 1-143, 1-144, 1-149, 1-15, 1-151, 1-154, 1-156, 1-157, 1-158, 1-159, 1-16, 1-160, 1-161, 1-162, 1-163, 1-164, 1-165, 1-167, 1-169, 1-170, 1-172, 1-173, 1-174, 1-175, 1-176, 1-177, 1-178, 1-179, 1-180, 1-181, 1-183, 1-184, 1-185, 1-186, 1-187, 1-188, 1-189, 1-19, 1-190, 1-191, 1-192, 1-193, 1-194, 1-195, 1-2, 1-20, 1-21, 1-25, 1-29, 1-3, 1-30, 1-33, 1-34, 1-37, 1-38, 1-4, 1-40, 1-43, 1-44, 1-45, 1-46, 1-47, 1-48, 1-49, 1-5, 1-52, 1-56, 1-58, 1-6, 1-60, 1-61, 1-64, 1-67, 1-68, 1-69, 1-7, 1-70, 1-71, 1-83, 1-84, 1-87, 1-9, 1-111, 1-112, 1-113, 1-72, 1-73, 1-74, 1-75, 1-76, 1-78, 1-82, 1-83, 1-85, 1-86, 1-88, 1-89, 1-99
    • Spodoptera Frugiperda Test (Spray Treatment)
  • Solvents: 78 parts by weight of acetone
      • 1.5 parts by weight of dimethylformamide
        Emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of maize leaves (Zea mays) are sprayed with an active compound preparation of the desired concentration and, after drying, populated with caterpillars of the armyworm (Spodoptera frugiperda).
  • After 7 days, the activity in % is determined. 100% means that all caterpillars have been killed; 0% means that none of the caterpillars has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 500 ppm:
  • Ex. Nos.: 1-1, 1-10, 1-11, 1-114, 1-115, 1-12, 1-123, 1-124, 1-126, 1-127, 1-129, 1-13, 1-130, 1-131, 1-132, 1-133, 1-134, 1-135, 1-139, 1-14, 1-143, 1-146, 1-147, 1-149, 1-15, 1-151, 1-152, 1-155, 1-159, 1-16, 1-160, 1-164, 1-167, 1-170, 1-172, 1-173, 1-174, 1-176, 1-177, 1-183, 1-185, 1-186, 1-187, 1-188, 1-189, 1-19, 1-190, 1-191, 1-192, 1-2, 1-20, 1-21, 1-22, 1-25, 1-29, 1-3, 1-30, 1-4,1-5, 1-6, 1-67, 1-7, 1-70, 1-71, 1-8, 1-9, 1-111, 1-72, 1-73, 1-74, 1-75, 1-76, 1-81, 1-83, 1-85, 1-86, 1-99
    • Tetranychus Test, OP-Resistant (Spray Treatment)
  • Solvents: 78 parts by weight of acetone
      • 1.5 parts by weight of dimethylformamide
        Emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Discs of bean leaves (Phaseolus vulgaris) infested by all stages of the greenhouse red spider mite (Tetranychus urticae) are sprayed with an active compound preparation of the desired concentration.
  • After 6 days, the activity in % is determined. 100% means that all spider mites have been killed; 0% means that none of the spider mites has been killed.
  • In this test, for example, the following compounds of the Preparation Examples exhibit an activity of ≧80% at an application rate of 500 ppm:
  • Ex. Nos.: 1-116, 1-192, 1-199, 1-5, 1-83
    • Boophilus Microplus—Test (Injection)
  • Solvent: dimethyl sulfoxide
  • To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with solvent to the desired concentration. Five adult engorged female ticks (Boophilus microplus) are injected with 1 n1 compound solution into the abdomen. Ticks are transferred into replica plates and incubated in a climate chamber for a period of time. Egg deposition of fertile eggs is monitored.
  • After 7 days mortality in % is determined. 100% means that all eggs are infertile; 0% means that all eggs are fertile.
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 20 μg/animal:
  •
    1-222
    1-224
    1-225
    1-235
    1-245
    1-254
    1-274
    1-299
    • Lucilia Cuprina (48 h)
  • species: Lucilia cuprina 1st instar larvae (age 24 hrs)
    Solvent: dimethyl sulfoxide
  • 10 mg active compound are dissolve in 0,5 ml Dimethylsulfoxid. Serial dilutions are made to obtain the desired rates. Approximately 20-30 Lucilia cuprina 1st instar larvae are transferred into a test tube containing 1 cm3 of minced horse meat and 0.5 ml aqueous dilution of test compound. After 48 hrs percentage of larval mortality are recorded. 100% efficacy=all larvae are killed, % efficacy normally developed larvae after 48 hrs.
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 100 ppm:
  •
    1-127
    1-131
    1-132
    1-147
    1-172
    1-176
    1-222
    1-224
    1-225
    1-230
    1-234
    1-235
    1-238
    1-239
    1-245
    1-246
    1-254
    1-255
    1-258
    1-274
    1-279
    1-299
    1-305
    1-308
    1-326
    7-1
    7-2
    7-20
    • Musca Domestica—Test
  • Solvent: dimethyl sulfoxide
  • To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 ml solvent, and the concentrate is diluted with water to the desired concentration. Prior to the assay, a piece or kitchen sponge is soaked with a mixture of sugar and compound solution and placed into a container. 10 adults (Musca domestica) are placed into the container and closed with a perforated lid. After 2 days mortality in % is determined. 100% means that all the flies have been killed; 0% means that none of the flies have been killed.
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 100 ppm:
  •
    1-147
    1-172
    1-234
    1-238
    1-239
    1-245
    1-246
    1-254
    1-255
    1-258
    1-274
    1-279
    1-258
    1-274
    1-279
    7-2
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 20 ppm:
  • 1-127, 1-222, 1-224, 1-225, 1-230, 1-299, 7-20
    • Myzus Persicae—Test; (Spray Application) 2
  • Solvent: 78.0 parts by weight acetone
      • 1.5 parts by weight dimethylformamide
        Emulsifier: 0.5 parts by weight alkylarylpolyglcolether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. Chinese cabbage (Brassica pekinesis) leaf-disks infected with all instars of the green peach aphid (Myzus persicae), are sprayed with a preparation of the active ingredient at the desired concentration.
  • After 6 days mortality in % is determined. 100% means that all aphids have been killed; 0% means that none of the aphids have been killed.
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 500 g/ha:
  •
    1-22
    1-222
    1-223
    1-224
    1-225
    1-226
    1-229
    1-230
    1-231
    1-235
    1-236
    1-239
    1-242
    1-246
    1-254
    1-258
    1-261
    1-271
    1-272
    1-274
    1-275
    1-276
    1-277
    1-278
    1-279
    1-289
    1-299
    1-301
    1-307
    1-308
    1-314
    1-316
    1-322
    1-325
    1-326
    3-1
    3-4
    3-5
    3-6
    3-7
    3-8
    3-11
    3-12
    7-1
    7-2
    7-7
    7-20
    7-21
    7-23
    9-1
    • Phaedon Cochleariae —Test; (Spray Application)
  • Solvent: 78.0 parts by weight of acetone
      • 1.5 parts by weight of dimethylformamide
        Emulsifier: 0.5 parts by weight of alkylaryl polyglycolether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
  • Chinese cabbage (Brassica pekinesis) leaf-disks are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf disks are infested with mustard beetle larvae (Phaedon cochleariae).
  • After 7 days mortality in % is determined. 100% means that all beetle larvae have been killed and 0% means that none of the beetle larvae have been killed.
  • In this test for example, the following compounds from the preparation examples showed good activity of ≧80% at application rate of 500 g/ha:
  •
    1-221
    1-222
    1-223
    1-224
    1-225
    1-226
    1-227
    1-229
    1-230
    1-231
    1-235
    1-236
    1-238
    1-239
    1-241
    1-242
    1-246
    1-250
    1-254
    1-255
    1-256
    1-258
    1-260
    1-261
    1-263
    1-265
    1-271
    1-274
    1-275
    1-276
    1-277
    1-278
    1-279
    1-280
    1-281
    1-282
    1-283
    1-284
    1-285
    1-289
    1-293
    1-294
    1-295
    1-296
    1-297
    1-298
    1-299
    1-300
    1-301
    1-302
    1-303
    1-304
    1-307
    1-308
    1-315
    1-320
    1-321
    1-322
    1-325
    1-326
    1-327
    1-328
    1-329
    1-330
    1-331
    1-332
    3-13
    3-7
    3-8
    3-9
    7-1
    7-10
    7-11
    7-13
    7-14
    7-15
    7-16
    7-17
    7-18
    7-2
    7-20
    7-21
    7-22
    7-24
    7-25
    7-3
    7-4
    7-5
    7-6
    7-7
    7-8
    7-9
    9-1
    9-2
    9-3
    9-4
    • Spodoptera Fragiperda—Test (Spray Application)
  • Solvent: 78.0 parts by weight acetone
      • 1.5 parts by weight dimethylformamide
        Emulsifier: 0.5 parts by weight alkylarylpolyglcolether
  • To produce a suitable preparation of the active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is dilutes with emulsifier-containing water to the desired concentration. Maize (Zea mais) leaf sections are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf sections are infested with fall armyworm larvae (Spodoptera frugiperda).
  • After 7 days mortality in % is determined. 100% means that all caterpillars have been killed and 0% means that none of the caterpillars have been killed.
  • In this test for example, the following compounds from the preparation examples showed good activity≧80% at application rate of 500 g/ha:
  •
    1-221
    1-222
    1-224
    1-225
    1-226
    1-227
    1-228
    1-229
    1-230
    1-231
    1-235
    1-236
    1-238
    1-239
    1-241
    1-242
    1-246
    1-250
    1-254
    1-255
    1-256
    1-258
    1-260
    1-261
    1-262
    1-263
    1-270
    1-271
    1-272
    1-274
    1-276
    1-277
    1-278
    1-293
    1-294
    1-294
    1-295
    1-296
    1-298
    1-299
    1-301
    1-302
    1-303
    1-304
    1-307
    1-308
    1-314
    1-315
    1-316
    1-321
    1-322
    1-325
    1-326
    1-327
    1-328
    1-329
    1-330
    1-331
    3-10
    3-12
    3-13
    3-14
    3-15
    3-7
    3-9
    7-19
    7-2
    7-20
    7-21
    7-22
    7-23
    7-24
    7-25
    7-4
    7-7
    7-8
    • Tetranychus Urticae—Test; OP-Resistant (Spray Application)
  • Solvent: 78.0 parts by weight acetone
      • 1.5 parts by weight dimethylformamide
        Emulsifier: 0.5 parts by weight alkylarylpolyglcolether
  • To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. French beans (Phaseolus vulgaris) which are heavily infested with all stages of the two spotted spidermite (Tetranychus urticae), are sprayed with a preparation of the active ingredient at the desired concentration.
  • After 6 days mortality in % is determined. 100% means that all spider mites have been killed and 0% means that none of the spider mites have been killed.
  • In this test for example, the following compounds from the preparation examples showed good activity≧80% at application rate of 500 g/ha:
  •
    1-258
    1-265
    1-275
    1-320
    1-332
    7-2
  • Unless not mentioned otherwise, the test solutions were prepared as follows:
  • Containing as solvent: Dimethylformamide, 3 parts by weight; and as emulsifier: Polyoxyethylene alkyl phenyl ether, 1 part by weight
  • To prepare the test solution, 1 part by weight of an active compound is mixed with the above-mentioned amount of solvent containing the above-mentioned amount of emulsifier, and the mixture is diluted with water to the desired concentration.
  • Test Against Tobacco Cutworm (Spodoptera litura) Larvae
  • Leaves of sweet potato were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then placed in a petri dish having a diameter of 9 cm, and ten Spodoptera litura at third instar larvae were released therein. The petri dishes were placed in a temperature-controlled chamber at 25° C. After 2 days and 4 days more sweet potato leaves were added. After 7 days, the number of dead larvae was counted to calculate the insecticidal activity. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed. In the current test, the results of two petri dishes for each treatment were averaged.
  • In the biological test example 1, the compounds Nos. 1-177, 1-190, 1-232, 1-234, 1-235, 1-236, 1-237, 1-238, 1-239, 1-240, 1-241, 1-242, 1-243, 1-244, 1-245, 1-246, 1-247, 1-248, 1-252, 1-253, 1-254, 1-257, 1-258, 1-259, 1-264, 1-265, 1-266, 1-267, 1-268, 1-269, 1-286, 1-288, 1-305, 1-310, 1-311, 1-312, 1-313, 1-314, 1-317, 1-318, 1-319, 1-324, 1-325, 1-326 and 5-2 showed an insecticidal activity of 100% at an active compound concentration of 100 ppm,
  • Test Against Cucurbit Leaf Beetle (Aulacophora femoralis)
  • Leaves of cucumber were immersed in the test solution at the appropriate concentration, and the leaves were dried in air. The leaves were then put in a plastic cup containing sterilized black soil and five Aulacophora femoralis at second instar larvae were released in the cup. The cups were placed in a temperature-controlled chamber at 25° C. After 7 days, the number of dead larvae was counted, and thus the insecticidal activity was calculated. An insecticidal activity of 100% means that all larvae were killed, whereas an insecticidal activity of 0% means that no larva was killed.
  • In the biological test example 2, the compounds Nos. 1-177, 1-190, 1-232, 1-233, 1-234, 1-235, 1-236, 1-237, 1-238, 1-239, 1-240, 1-241, 1-242, 1-243, 1-244, 1-245, 1-246, 1-247, 1-248, 1-249, 1-251, 1-252, 1-253, 1-254, 1-256, 1-257, 1-258, 1-259, 1-260, 1-261, 1-264, 1-265, 1-266, 1-267, 1-268, 1-269, 1-270, 1-273, 1-286, 1-287, 1-288, 1-290, 1-291, 1-292, 1-305, 1-306, 1-309, 1-310, 1-311, 1-312, 1-314, 1-318, 1-319, 1-322, 1-324, 1-325, 1-326, 3-13, 3-16, 5-1, 5-2, 5-3, 5-5, 5-6 and 5-8
  • showed an insecticidal activity of 100% at an active compound concentration of 500 ppm.

Claims (6)

1. Compounds of the formula (I)
Figure US20120071496A1-20120322-C00098
in which
R1 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, halocycloalkylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl.
R2 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
R3 represents a radical from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, cyanoalkyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylsulphanylalkyl, alkylsulphinylalkyl, alkylsulphonylalkyl, haloalkylsulphanylalkyl, haloalkylsulphinylalkyl, haloalkylsulphonylalkyl, cycloalkylalkyl and in each case optionally substituted phenyl, naphthyl, phenylalkyl, heteroaryl, heteroarylalkyl, heterocyclyl and hererocyclylalkyl,
R4 represents a radical from the group consisting of in each case optionally substituted phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
R5 represents a radical from the group consisting of hydrogen, halogen, cyano and in each case optionally substituted alkyl, cycloalkyl, phenyl, naphthyl, heteroaryl, heteroarylalkyl, heterocyclyl and heterocyclylalkyl,
R6 represents a radical from the group consisting of hydrogen, halogen, alkyl, haloalkyl, cyanoalkyl, alkoxyalkyl, alkylcarbonyl, haloalkylcarbonyl, cycloalkyl, halocycloalkyl, cycloalkylalkyl, alkylsulphonyl, alkenyl, alkynyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, alkoxycarbonylalkyl; optionally substituted phenyl, optionally substituted naphthyl, optionally substituted phenylalkyl, optionally substituted heterocyclylalkyl, optionally substituted heteroarylalkyl and optionally substituted phenylcarbonyl and
X represents oxygen or sulphur.
2. Composition, characterized in that it comprises at least one compound of the formula (I) according to claim 1 and customary extenders and/or surfactants.
3. Method for controlling pests, characterized in that a compound of the formula (I) according to claim 1 or a composition according to claim 2 is allowed to act on the pests and/or their habitat.
4. Use of compounds of the formula (I) according to claim 1 or of compositions according to claim 2 for controlling pests.
5. Pharmaceutical compositions comprising at least one compound according to claim 1.
6. Use of at least one compound according to claim 1 for preparing pharmaceutical compositions for controlling parasites on animals.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9107923B2 (en) 2013-06-27 2015-08-18 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US11730009B2 (en) 2015-09-24 2023-08-15 Lg Chem, Ltd. Compound and organic light-emitting element comprising same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11377438B2 (en) 2018-11-02 2022-07-05 Merck Sharp & Dohme Llc 2-amino-n-heteroaryl-nicotinamides as Nav1.8 inhibitors

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003013484A2 (en) * 2001-08-07 2003-02-20 F. Hoffmann-La Roche Ag N-monoacylated derivatives of o-phenylenediamines, their six membered heterocyclic analogues and their use as pharmaceutical agents

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3347290A1 (en) 1983-12-28 1985-07-11 Dr. Karl Thomae Gmbh, 7950 Biberach NEW 2-PHENYL IMIDAZOLES, THEIR PRODUCTION AND MEDICINES CONTAINING THESE COMPOUNDS
JP2556100B2 (en) 1988-03-15 1996-11-20 住友化学工業株式会社 Method for producing substituted nicotinic acid ester
KR100239800B1 (en) * 1996-11-28 2000-03-02 손경식 4,5-diaminopyrimidine derivatives and its preparation
AU4678699A (en) 1998-06-10 1999-12-30 Boulder Scientific Company Synthesis of aryl boronic acids
DE60022366T2 (en) * 1999-07-02 2006-06-14 Eisai Co Ltd CONDENSED IMIDAZOLE DERIVATIVES AND MEDICAMENTS AGAINST DIABETES MELLITUS
DE10108481A1 (en) 2001-02-22 2002-10-24 Bayer Ag pyridylpyrimidines
US7129239B2 (en) * 2002-10-28 2006-10-31 Pfizer Inc. Purine compounds and uses thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003013484A2 (en) * 2001-08-07 2003-02-20 F. Hoffmann-La Roche Ag N-monoacylated derivatives of o-phenylenediamines, their six membered heterocyclic analogues and their use as pharmaceutical agents

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
International Preliminary Report on Patentability, PCT/EP2010/000719 (Aug. 23, 2011) *

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9107923B2 (en) 2013-06-27 2015-08-18 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US9139561B2 (en) 2013-06-27 2015-09-22 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US9527831B2 (en) 2013-06-27 2016-12-27 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US9822097B2 (en) 2013-06-27 2017-11-21 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US10093655B2 (en) 2013-06-27 2018-10-09 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US10421744B2 (en) 2013-06-27 2019-09-24 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US10696658B2 (en) 2013-06-27 2020-06-30 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US11014909B2 (en) 2013-06-27 2021-05-25 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US11964961B2 (en) 2013-06-27 2024-04-23 Pfizer Inc. Heteroaromatic compounds and their use as dopamine D1 ligands
US11730009B2 (en) 2015-09-24 2023-08-15 Lg Chem, Ltd. Compound and organic light-emitting element comprising same

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