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WO1993015073A1 - Azabricyclic compounds as calcium channel antagonists - Google Patents

Azabricyclic compounds as calcium channel antagonists Download PDF

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Publication number
WO1993015073A1
WO1993015073A1 PCT/GB1993/000175 GB9300175W WO9315073A1 WO 1993015073 A1 WO1993015073 A1 WO 1993015073A1 GB 9300175 W GB9300175 W GB 9300175W WO 9315073 A1 WO9315073 A1 WO 9315073A1
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Prior art keywords
formula
azabicyclo
octane
compound
group
Prior art date
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PCT/GB1993/000175
Other languages
French (fr)
Inventor
Barry Sidney Orlek
Thomas Henry Brown
David Gwyn Cooper
Original Assignee
Smithkline Beecham Plc
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Publication date
Application filed by Smithkline Beecham Plc filed Critical Smithkline Beecham Plc
Priority to EP93902471A priority Critical patent/EP0625979A1/en
Priority to JP5513049A priority patent/JPH07503463A/en
Publication of WO1993015073A1 publication Critical patent/WO1993015073A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
    • A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08—Bridged systems

Definitions

  • the present invention relates to the use of known and novel azabicyclic derivatives in therapy, in particular as calcium channel antagonists, novel compounds pa: .S£ » processes for their preparation, and pharmaceutical compositions containing them.
  • Rj is inter alia hydrogen
  • R-2 is hydrogen or ALK-Z
  • R3 is hydrogen or ALK"-Z
  • ALK is C2-4alkyl
  • ALK" is Cj ⁇ alkyl
  • Z is a mono- or- di-substituted phenyl ring.
  • Ricciardi and Doukas (Heterocycles, Vol 24, No 4, p971, 1986) describe certain styrylquinuclidines, which are said to inhibit cholineacetyl-transferase in vitro.
  • German OLS 41 16582 describes azabicyclic compounds of the formula
  • A, B and C independently represent -CH2- or a single bond; n is zero, 1 or 2; X is oxygen or sulphur and R is inter alia phenylalkyl, diphenylalkyl, heterocyclicalkyl, phenyl, diphenyl or a heterocycle, each of which may be optionally substituted. These compounds are said to be useful as muscaiinic antagonists.
  • EPA 497415 describes 3-(substituted phenoxy and substituted phenylthio)quinuclidines, wherein the phenyl substitutent is selected from inter alia lower alkoxy, lower aralkyloxy, halogen, NO2, CF3, CN and NRjR2, which compounds are said to be muscarinic agonists.
  • certain substituted azabicyclic derivatives including some of the above compounds, exhibit activity as calcium channel antagonists. They are thus of potential use in the treatment of disorders where calcium channel blockade is indicated, in particular disorders related to an accumulation of calcium in the brain cells of mammals.
  • the present invention therefore provides, in a -first aspect, the use of a compound of formula (I):
  • n is 0 to 6, and m is 0 to 6, such that the length of the chain -(CH2) n A(CH2) m is at least two atoms;
  • Ar is aryl or heteroaryl, each of which may be optionally substituted
  • the H atom is shown on the bridgehead carbon atom to make clear that the (CH2) n A(CH2) m Ar chain cannot be attached at this position.
  • the compounds of formula (I) have been found to exhibit high calcium influx blocking activity for example in neurons.
  • the compounds are expected to be of use in therapy, particularly in treating conditions and diseases related to (e.g. caused or exacerbated by) an accumulation of calcium in the brain cells of mammals, in particular humans.
  • the compounds are expected to be of use in the treatment of anoxia, ischaemia including for example stroke, migraine, epilepsy, traumatic head injury, AEDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age- related memory disorders, and drug addiction withdrawal such as ethanol addiction withdrawal.
  • the present invention provides a method of treatment of anoxia, ischaemia including for example stroke, migraine, epilepsy, traumatic head injury, AIDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age- related memory disorders, and drug addiction withdrawal such as ethanol addiction withdrawal, which comprises administering to a subject in need thereof, an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
  • p and r are preferably independently 2 or 3; most preferably both are 2.
  • q is preferably 1 or 2.
  • n and m should be chosen such that the length of the chain (CH2) n A(CH2) m is at least 2 atoms. In general the length of the chain -(CH2) n A(CH2) m is from 2 to 6 e.g. 2 to 5 atoms. Preferred values for n and m depend on the group A. Thus for example when A is oxygen the sum of n+m is preferably from 1 to 5, for example n may be 1, 2, 3 or 4 and m may be 0 or 1.
  • n+m When A is a bond the sum of n+m should be at least 2, e.g. n+m may be 2 or 3.
  • a is CH CH one or both of n and m may be zero, e.g. n may be zero or 1 and m may be zero.
  • suitable groups include, for example, unsaturated monocyclic and unsaturated or partially saturated bicyclic or tricyclic ring systems of up to 15 carbon atoms, such as, for example, phenyl, naphthyl, tetrahydronaphthyl, fluorene, fluorenone, dibenzosuberene and dibenzosuberenone. Preferred are optionally substituted phenyl rings.
  • An aryl group may be substituted, for example, by a C ⁇ _2alkylenedioxy group (e.g.
  • Suitable optionally substituted phenylC ⁇ _4alkyl groups include, for example benzyl.
  • Suitable optionally substituted phenylC ⁇ _4alkoxy groups include, for example benzyloxy groups.
  • Suitable substituents for said optionally substituted phenyl, phenoxy, phenylC ⁇ alkyl and phenylC ⁇ _4alkoxy groups include for example halogen, Cj ⁇ alkyl, Cj ⁇ alkoxy, nitro and trifluoromethyl groups.
  • the aryl group is a phenyl ring substituted by one or two substituents, in particular, by a phenyl; phenyl(C ⁇ _4)alkyl, e.g. benzyl or phenethyl; phenoxy; or phenylC ⁇ _4alkoxy group; which groups may themselves be optionally substitued by halo, e.g. chloro.
  • suitable groups include, for example, unsaturated or partially saturated bicyclic and tricyclic ring systems containing at least one heteroatom.
  • a bicyclic ring system preferably contains 8 to 10 ring members, such as quinolinyl, tetrahydroquinolinyl or benzofuranyl.
  • a tricyclic ring system preferably contains from 11 to 15 ring members, and most preferably has the structure :
  • Y 1 represents Y(C ._2) t
  • Y is O, S or NR ⁇ (where R ⁇ is hydrogen or Ci ⁇ alkyl)
  • s is 0, 1 or 2
  • t is 0 or 1 or is a corresponding dehydro ring system.
  • tricyclic heteroaryl groups include dibenzofuranyl, dibenzothienyl, carbazole, N-methylcarbazole, acridine and dibenzoxepine.
  • the heteroaryl ring can be linked to the remainder of formula (I) via any suitable ring atom.
  • Suitable substituents for said heteroaryl rings include, for example, 1 to 3 substituents selected from halogen, trifluoromethyl, Cj.4alkyl, C ⁇ _4alkoxy, phenyl, phenylCj ⁇ alkyl and phenylC ⁇ _4alkoxy.
  • Alkyl groups present in the compounds of formula (I), alone or as part of another group, can be straight or branched.
  • a Cj ⁇ alkyl group may be for example methyl, ethyl, n-propyl, n-butyl or any branched isomer thereof such as isopropyl or t-butyl.
  • a salt of a compound (I) should be pharmaceutically acceptable.
  • pharmaceutically acceptable salts include inorganic and organic acid addition salts such as hydrochloride, hydrobromide, sulphate, phosphate, acetate, fumarate, maleate, citrate, lactate, tartrate, oxalate, methanesulphonate or similar pharmaceutically acceptable inorganic or organic acid addition salts.
  • Other non- pharmaceutically acceptable salts may be used for example in the isolation of a final product and are included within the scope of this invention.
  • the invention also provides novel compounds of formula (IA) :
  • n is 0 to 6
  • m is 0 to 6, and either
  • A is -C ⁇ C- or NRl, where R* is hydrogen, C j .galkyl or phenylCj_4alkyl; in which case Ar represents the group Ar as hereinbefore defined;
  • Ar ⁇ represents a group Ar 2 which is phenyl substituted by a C ⁇ _2alkylenedioxy group or by 1 to 3 substituents selected from SC ⁇ _4alkyl, OCF3, Q ⁇ optionally substituted phenoxy, optionally substituted phenylC ⁇ _4alkyl and optionally substituted phenylC ⁇ _4alkoxy; or Ar 2 is
  • Suitable substituents for said optionally substituted phenoxy, phenylC ⁇ alkyl and phenylC ⁇ _4alkoxy groups are as hereinbefore defined.
  • Bicyclic and tricyclic aryl and heteroaryl groups for Ar* and Ar 2 include those defined hereinbefore for the group Ar.
  • p and r are preferably 2 or 3; q is preferably 1 or 2.
  • a bicyclic aryl group is preferably naphthyl.
  • a bicyclic heteroaryl group is preferably benzofuranyl.
  • a tricyclic heteroaryl group is preferably dibenzofuranyl.
  • a particular group of compounds according to the invention is that represented by formula (IB)
  • R ⁇ represents optionally substituted phenoxy, optionally substituted phenylC ⁇ _4alkyl or optionally substituted phenylC ⁇ _4alkoxy, or R ⁇ represents a fused benzene ring; and salts thereof.
  • A represents oxygen
  • R preferably represents benzyl, benzyloxy or phenoxy, or is a fused benzene ring.
  • Particular compounds of the invention include:
  • the compounds of the present invention can be prepared by processes analogous to those known in the art.
  • the present invention therefore provides in a further aspect, a process for the preparation of a compound of formula (I) which comprises:
  • L(CH2)mAr can take place under conditions which depend on the nature of the group L and the value of m.
  • the reaction is carried out under standard conditions in a solvent, optionally in the presence of a base.
  • a fluoro-substituted aryl compound F-Ar is employed in process (a) (to prepare compounds where m is zero)
  • the reaction is effected in the presence of a strong base such as sodium hydride, and in an inert organic solvent such as dimethylformamide.
  • a strong base such as sodium hydride
  • an inert organic solvent such as dimethylformamide.
  • the aryl group is substituted by an activating group such as CF3 or NO2.
  • the azabicyclic nitrogen atom may be protected during the reaction by methods well known in the art, e.g. by prior formation of a quaternary derivative such as an N-benzyl derivative. Protection may also be effected by formation of a borane (BH3) complex.
  • the N- protecting group should be chosen such that it can be removed without affecting other moieties in the molecule.
  • a benzyl protecting group may not be appropriate when the side chain (CH2) n A(CH2) m Ar also contains a benzyl moiety such as a benzyloxy group.
  • N-protection is preferred when the leaving group L represents halogen, e.g. bromine, but when L is a sulphonic acid residue e.g. a tosylate, N- protection may not be necessary.
  • reaction between a compound of formula (El) and a compound of formula HAl(CH2) m Ar can take place under conditions which depend on the nature of i and A.
  • i hydroxy
  • m 0
  • a ⁇ oxygen or sulphur
  • the reaction is carried out in the presence of diethyl azodicarboxylate and triphenyl phosphine.
  • the leaving group l ⁇ may be for example a halogen atom or a sulphonyloxy group eg. methane-sulphonyloxy or p-toluene sulphonyloxy in which case the compound (HI) may preferably be protected, e.g. as an acid salt, such as a hydrochloride salt
  • Reaction may be effected in the presence or absence of solvent, at a temperature in the range 0 to 200°C and may preferably be carried out in the presence of a base.
  • a compound of formula (IV) can be effected by methods known in the art, for example using a reducing agent such as lithium aluminium hydride.
  • a compound of formula (IV) can be prepared (for example as described below) and reduced in a 'one-pot' reaction, without isolation of compound ON) itself.
  • reaction between a compound of formula (N) in process (d) and a compound of formula X ⁇ Ar can take place under standard conditions known to those skilled in the art for the formation of carbon-carbon bonds.
  • Process (e) may be effected using a Wadsworth-Emmons reagent of the formula Ar(CH2) m +iP(O)(OAlk)2, such as a diethylphosphonate, or a Wittig reagent of the formula Ar(CH2) + ⁇ PPh3X (where X is an anion) which compounds are available commercially or can be prepared by known methods.
  • the reaction may be carried out in a solvent such as tetrahydrofuran optionally containing a crown ether such as 15-crown-5, or 18-crown-6, and in the presence of a strong base such as sodium hydride or potassium t-butoxide.
  • Interconversion reactions according to process (f) may be effected by methods well known in the art.
  • Esters wherein n is greater than 1 may be prepared by conversion of an ester wherein n is 1 to the corresponding N-methyl-N-methoxycarboxamide (e.g. by hydrolysis of the ester followed by reaction with thionyl chloride and N, O-dimethylhydroxylamine hydrochloride), which is then reduced to the aldehyde using diisobutylaluminium hydride.
  • the aldehyde is further converted to the cyanomethyl derivative for example as described in EPA 363,085, followed by acid hydrolysis, and esterification to form an ester wherein n is 2.
  • the sequence may be repeated to form higher homologues.
  • Homologation may also be effected by the method described in British Patent No. 1250534, starting with a compound ( ⁇ ) wherein A is O and n is 1 and proceeding via the corresponding halomethyl and cyanomethyl derivatives to an ester of formula (VII) wherein n is 2 which may be reduced to an alcohol (II) wherein n is 2.
  • a further method for the preparation of a compound of formula (II) wherein p, q, r and n each represent 2, A* is oxygen and the group (CH2) n AlH is ⁇ to the ring nitrogen atom involves cyclisation of a 4-piperidyl-but-2-enoic acid ester e.g. a methyl ester.
  • the cyclisation is an intramolecular Michael reaction which may be carried out at elevated temperature in an inert solvent such as refluxing toluene.
  • Methyl 4-piperidyl-but-2-enoate may be obtained from a suitable N-protected precursor such as methyl 4-(4-N-tert- butyloxycarbonylpiperidyl)-but-2-enoate (which may be prepared as described in EP 478363), using e.g. trifluoroacetic acid optionally in a solvent such as dichloromethane.
  • Reduction e.g. with lithium aluminium hydride provides the above mentioned compound of formula (II).
  • triethylphosphonoacetate or triethylphosphonocrotonate followed by catalytic hydrogenation to give an ethoxycarbonylalkyl derivative which is further reduced e.g. using lithium aluminium hydride, to the desired hydroxyalkyl compound.
  • ethoxycarbonylalkyl derivative which is further reduced e.g. using lithium aluminium hydride, to the desired hydroxyalkyl compound.
  • Ketones of formula (VHI) are commercially available or can be prepared by literature methods, generally via a Dieckmann cyclisation, (for example as described in EPA 94742).
  • Compounds of formula (II) wherein A is S or NR ⁇ may be prepared from the corresponding hydroxy compound by standard methods, for example via formation of an alkyl halide followed by reaction with an appropriate amine or thiol.
  • Compounds of formula (HI) wherein L* is OH can be prepared as described for compounds of formula (II), and compounds of formula (III) wherein i is a halogen atom, or a mesyloxy or tosyloxy group can be prepared from the corresponding alcohol in conventional manner.
  • the compounds of formula L(CH2) m Ar and HAl(CH2) m Ar may be prepared by standard methods well known in the art.
  • compounds L(CH2) Ar wherein Ar is a substituted phenyl group and L is halo, e.g. bromo may be prepared by Friedel-Crafts acylation of the corresponding substituted benzene derivative, using an appropriate acid chloride and catalysed by aluminium trichloride, followed by reduction in ⁇ ilji with triethylsilane.
  • the starting materials are available commercially or may be prepared by standard methods, e.g. by reaction of 4-benzyloxybenzaldehyde with triethylphosphonocrotonate in a similar manner to that described for the preparation of compounds (II).
  • -(CH2) n N(R 1 )C(O)(CH2) m -lAr can be prepared by reacting a compound of formula (II) wherein A represents NR* with an acylating agent corresponding to the group - (CH2) m Ar, for example an acid chloride ClOC(CH2) m -iAr.
  • -(CH2) n -lC(O)N(Rl)(CH2) m Ar may be prepared for example by reaction of a corresponding compound wherein R ⁇ represents -(CH2) n _iCO2H or an activated derivative thereof such as an acid halide, ester or anhydride, with an amine of formula HN(Rl)(CH2) m Ar. It will be appreciated that when the acid itself is employed, reaction with the amine should be effected in the presence of a coupling agent.
  • the carboxylic acid may itself be prepared for example by oxidation of the corresponding alcohol, ie. a compound of formula (Q) wherein A* is oxygen.
  • Compounds of formula (V) may be prepared in analogous manner to compounds of formula H); where necessary the chain length may be increased using methods well known in the art.
  • Compounds of formula (VI) may be prepared by conventional methods, for example the oxidation of a compound of formula (II) wherein A ⁇ is oxygen, or conversion of the corresponding ester, e.g. by hydrolysis and subsequent reaction with thionyl chloride and N,O-dimethyl-hydroxylamine, followed by reduction of the resulting N-methyl- N-methoxy-carboxamide, using diisobutylaluminium hydride.
  • Compounds of formula (VI) wherein n is 1 may be prepared from the corresponding compound wherein n is zero by various methods.
  • the aldehyde wherein n is zero may be treated with (methoxymethyl) triphenylphosphonium chloride and potassium t-butoxide, followed by a strong acid, e.g. concentrated sulphuric acid, resulting in the aldehyde wherein n is 1.
  • a strong acid e.g. concentrated sulphuric acid
  • the aldehyde may be converted to the corresponding cyanomethyl derivative as described in EPA 363085 followed by acid hydrolysis, conversion to the N-methyl- N-methoxycarboxamide and reduction. These procedures may also be used to form higher homologues.
  • a compound of formula 0 When a compound of formula 0) is obtained as a mixture of enantiomers, these may be separated by conventional methods such as crystallisation in the presence of a resolving agent, or chromatography, for example using a chiral HPLC column.
  • the compounds of the present invention are usually administered in a standard pharmaceutical composition.
  • the present invention therefore provides in a further aspect pharmaceutical compositions comprising a novel compound of formula 0) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient
  • the compounds for use according to the invention may be administered by any convenient method for example by oral, parenteral, buccal, rectal or transdermal administration and the pharmaceutical compositions adapted accordingly.
  • the compounds of formula 0) and their pharmaceutically acceptable salts which are active when given orally can be formulated as liquids or solids, for example syrups, suspensions or emulsions, tablets, capsules and lozenges.
  • a liquid formulation will generally consist of a suspension or solution of the compound or pharmaceutically acceptable salt in a suitable liquid carrier(s) for example, ethanol, glycerine, non-aqueous solvent, for example polyethylene glycol, oils, or water with a suspending agent, preservative, flavouring or colouring agent.
  • a composition in the form of a tablet can be prepared using any suitable pharmaceutical carrier(s) routinely used for preparing solid formulations.
  • suitable pharmaceutical carrier(s) include magnesium stearate, starch, lactose, sucrose and cellulose.
  • a composition in the form of a capsule can be prepared using routine encapsulation procedures.
  • pellets containing the active ingredient can be prepared using standard carriers and then filled into a hard gelatin capsule; alternatively, a dispersion or suspension can be prepared using any suitable pharmaceutical ca ⁇ ier(s), for example aqueous gums, celluloses, silicates or oils and the dispersion or suspension then filled into a soft gelatin capsule.
  • Compounds for use according to the invention may also be administered parenterally, by bolus injection or continuous infusion.
  • Typical parenteral compositions consist of a solution or suspension of the compound or pharmaceutically acceptable salt in a sterile aqueous carrier or parenterally acceptable oil, for example polyethylene glycol, polyvinyl pyrrolidone, lecithin, arachis oil or sesame oil.
  • the solution can be lyophilised and then reconstituted with a suitable solvent just prior to administration.
  • Both liquid and solid compositions may contain other excipients known in the pharmaceutical art, such as cyclodextrins.
  • composition is in unit dose form such as a tablet, capsule or ampoule.
  • Each dosage unit for oral administration contains preferably from 1 to 250 mg (and for parenteral administration contains preferably from 0.1 to 60 mg) of a compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base.
  • the daily dosage regimen for an adult patient may be, for example, an oral dose of between 1 mg and 500 mg, preferably between 1 mg and 250 mg, eg. 5 to 200 mg or an intravenous, subcutaneous, or intramuscular dose of between 0.1 mg and 100 mg, preferably between 0.1 mg and 60 mg, eg. 1 to 40 mg of the compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base, the compound being administered 1 to 4 times per day.
  • the compounds of the invention may be administered by continuous intravenous infusion, preferably at a dose of up to 400 mg per day.
  • the total daily dosage by oral administration will be in the range 1 to 2000 mg and the total daily dosage by parenteral administration will be in the range 0.1 to 400 mg.
  • the compounds will be administered for a period of continuous therapy, for example for a week or more.
  • the pipette (internal solution) contained in mM: CsCl, 130; HEPES, 10; EGTA, 10; MgCL 2 , 4; ATP, 2; buffered to pH 7.2 with CsOH.
  • Cells were bathed in a normal Tyrodes solution before establishment of whole cell recording when the bathing solution was changed to one allowing isolation of Ca 2+ currents.
  • the external solution for recording Ca 2+ channel currents contained in mM: BaCL 2 , 10; TEA-C1, 130; glucose, 10; HEPES, 10; MgCL 2 , 1; buffered to pH 7.3 with TEA-OH. Barium was used as the charge carrier as this assists in current isolation and calcium dependent inactivation of current is avoided.
  • Peak voltage gated Ca 2+ channel currents of up to 10 nA from dorsal root ganglion neurons were recorded using 10 mM Ba 2+ as charge carrier. Currents were evoked from a holding potential of -80 mV to a test potential of 0 or +10 mV every 15 seconds. This test potential was at the peak of the current voltage relationship and assessing block at this point reduced any errors due to drifting holding potential. Some cells showed slow rundown of current as is commonly seen when recording Ca 2+ currents. The rundown rate was measured in control conditions and extrapolated through the time of drug application to derive a control value to relate the drug affected current to. Block by 20 mM drug was assessed 3 minutes after drug application.
  • a tonicity adjusting agent eg. sodium chloride, dextrose or mannitol may also be added.
  • the title compound was prepared in a similar manner to Preparation 1 from (+) 3- (3- ethoxycarbonylpropyl)-l-azabicyclo[2.2.2]octane (1.94g) and lithium aluminium hydride (1.21g, 32 mmol). This afforded the title compound as an oil (l.Og, 68% based on 3- quinuclidinone) which solidified on standing and was used in the next stage without purification.
  • the mixture was concentrated in vacuo and the residue was treated with 2M orthophosphoric acid (30ml), and washed exhaustively with diethyl ether.
  • the aqueous layer was saturated with potassium carbonate and extracted into chloroform (3x30ml).
  • the combined organic extracts were dried over sodium sulphate and concentrated in vacuo.
  • the crude product was purified by flash chromatography on neutral aluminia using 0-2% methanol in chloroform as eluant.
  • the major faster running component was hydrogenated in ethanol (25 ml) over 5% Pd-C (0.2g) at atmospheric pressure for 4h.
  • the catalyst was removed by filtration through kieselguhr, and the filtrate was concentrated in vacuo.
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (2g, 14.2mmol), 4-(benzyloxy)phenol (8.52g, 42.6mmol), triphenylphosphine (4.84g, 18.4mmol) and diethyl azodicarboxylate (3.21g, 18.4mmol). This afforded the title compound as a white solid (3g) m.p.205-207°C (from methanol-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), , 4-hydroxydiphenylmethane (0.98g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded die title compound as a white solid (0.46g) m.p. 169- 171°C (methanol-diethyl ether).
  • the title compound (E4) was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 2-phenylphenol (0.905g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound as a white solid (0.49g) m.p. 184-187°C (from methanol-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 4-tert-butylphenol (0.80g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound (E5) as a white solid (0.35g) m.p. 276- 279°C (from methanol-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 2-hydroxy-dibenzofuran (0.98g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and dietiiyl azodicarboxylate (0.81g, 4.61mmol).
  • the crude product was purified on neutral alumina in a gradient of 0- 2% methanol in toluene.
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 5-hydroxyisoquinoline (0.72g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and dietiiyl azodicarboxylate (0.8g, 4.61mmol). This afforded the title compound as a white solid (0.19g) m.p. 277-280°C (from methanol-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )endo-3- hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-hydroxydiphenylmethane (1.09g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and diethyl azodicarboxylate (0.89g, 5.12mmol). This afforded the title compound as a white solid (0.77g) m.p. 153-156°C (from methanol-acetone-diediyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )endo-3- hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-benzyloxyphenol (1.18g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and diethyl azodicarboxylate (0.89g, 5.12mmol). This afforded the title compound as a white solid (0.3 lg) m.p. 156-158°C (from methanol-acetone-diethyl ether).
  • the tide compound was prepared in a similar manner to Example 1 from ( ⁇ )exo- and endo-3-hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol),
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )exo- and endo-3-hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-benzyloxyphenol (1.18g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and dietiiyl azodicarboxylate (0.89g, 5.12mmol).
  • the crude product was chromatographed on silica in a gradient of 5- 20% methanol in chloroform. Pooling of pure fractions containing the major faster running component gave a gum which was converted into the hydrochloride salt to afford the title compound as a white solid (0.29g) m.p. 156-158°C (from methanol-acetone- diediyl ether).
  • the tide compound was prepared in a similar manner to Example 13 from 1- azabicyclo[2.2.2]oct-3-yl-carboxaldehyde (0.78g, 5.61mmol), dietiiyl 4-biphenylmethyl- phosphonate (1.70g, 5.61mmol), sodium hydride (0.17g of an 80% dispersion in mineral oil, 5.61mmol) and 15-crown-5 (60mg). This afforded the title compound as a white solid (1.3g) m.p. 289-290°C (from methanol-diethyl ether).
  • the tide compound was prepared in a similar manner to Example 15 from ( ⁇ )E-3-[2-(4- Biphenyl)ethenyl]-l-azabicyclo[2.2.2]octane hydrochloride (E14) (0.65g, 2mmol) and 10%Pd-C (65mg). This afforded the title compound as a white solid (0.14g) m.p. 236- 238 C (from methanol-acetone-dietiiyl ether).
  • the title compound was prepared in a similar manner to Example 13 from ( ⁇ )3- formylmethyl-l-azabicyclo[2.2.2]octane (0.41g, 2.68mmol), diethyl 1-naphthylmethyl- phosphonate (0.75g, 2.68mmol), sodium hydride (80mg of an 80% dispersion in mineral oil, 2.68mmol) and 15-crown-5 (30mg). This afforded the title compound as a white solid (0.47g) m.p. 174-177°C (from methanol-acetone-diethyl ether).
  • the tide compound was prepared in a similar manner to Example 1 from ( ⁇ )3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 2-hydroxydibenzofuran
  • the tide compound was prepared in a similar manner to Example 1 from ( ⁇ )3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 4-benzyloxyphenol (lg, 4.84mmol), triphenylphosphine (l.Olg, 4.19mmol) and dietiiyl azodicarboxylate (0.73g, 4.19mmol). This afforded the title compound as a white solid (0.5g) m.p.215-216°C (from methanol-acetone-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 4-hydroxydiphenylmethane (0.89g, 4.84mmol), triphenylphosphine (l.Olg, 4.19mmol), and dietiiyl azodicarboxylate (0.73g, 4.19mmol). This afforded the title compound as a white solid (0.69g) m.p 186- 188 C (from methanol-acetone-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 4-phenoxyphenol (0.99g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound as a white solid (0.59g) m.p 176-178°C (methanol-acetone-diediyl ether.
  • the title compound was prepared in a similar manner to Example 1 from (+) 3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.22mmol), 4-phenoxyphenol (0.90g, 4.84 mmol), triphenylphosphine (l.Og, 4.19 mmol) and diethyl azodicarboxylate 0.66 ml, 4.19 mmol). After stirring at room temperature for 2h, the reaction was concentrated in vacuo. The residue was extracted into diethyl etiier, and treated with ethereal hydrogen chloride.
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ ) 3-(4- hydroxybutyl)-l-azabicyclo[2.2.2]octane (0.5g, 2.73 mmol), 2-hydroxydibenzofuran (0.75g, 4.09 mmol), triphenylphosphine (0.93g, 3.55 mmol) and diethyl azodicarboxylate (0.56 ml, 3.55 mmol). After stirring at room temperature for lh the reaction was concentrated in vacuo. The crude product was converted into the hydrochloride salt, washed with diethyl ether, then partitioned betwen saturated aqueous potassium carbonate (25 ml) and chloroform (25 ml).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ )3-(3- hydroxypropyl)-l-azabicyclo[2.2.2]octane (0.45g, 2.66 mmol), 4-phenoxyphenol (0.74g, 3.98 mmol), triphenylphosphine (0.91g, 3.47 mmol) and diethyl azodicarboxylate (0.55 ml, 3.47 mmol). After stirring at room temperature for lh the reaction was worked up as described in Example 24.
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ ) 3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23 mmol), trans 4-hydroxystilbene (0.95g, 4.84 mmol), triphenylphosphine (l.lg, 4.19 mmol) and diethyl azodicarboxylate (0.66 ml, 4.19 mmol). After stirring at room temperature for 1.5h the reaction was concentrated in vacuo. The residue was extracted into diethyl ether and treated with ethereal hydrogen chloride to give the hydrochloride salt which was washed with diethyl ether.
  • the title compound was prepared in a similar manner to Example 1 from (+) 3-(2- hydroxyethylH-azabicyclo [2.2.2]octane (0.5g, 3.22 mmol), 4-[2-(4- chl ⁇ rophenyl)ethyl]phenol (1.13g, 4.86 mmol), triphenylphosphine (1.10g, 4.20 mmol) and diethyl azodicarboxylate (0.66 ml, 4.20 mmol). The reaction was worked up as described in Example 24.
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ ) 2-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (23mg, 0.15 mmol), 4-hydroxydiphenylmethane (41mg, 0.22 mmol), triphenylphosphine (59 mg, 0.22 mmol) and diethyl azodicarboxylate (39 mg, 0.22 mmol). After stirring at room temperature for 6h the reaction mixture was concentrated in vacuo. The residue was partitioned between water (5 ml) and chloroform (5ml) and the pH of the aqueous phase was adjusted to 12 with potassium carbonate.
  • the tide compound was prepared in a similar manner to Example 30 from ( ⁇ ) 2-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.22mmol), 4-benzyloxyphenol (0.97g, 4.84mmol), triphenylphosphine (1.27g, 4.84mmol) and diethyl azodicarboxylate (0.76ml, 4.84mmol). This afforded the tide compound as a colourless solid (0.69g) m.p.238- 240°C (from acetone-diethyl ether).
  • the title compound was prepared in a similar manner to Example 1 from ( ⁇ ) 4-(2- hydroxyethyl)-l-azabicyclo[3.3.1]nonane (O.llg, 0.65 mmol), 4-phenoxyphenol (0.18g, 0.98 mmol), triphenylphosphine (0.22g, 0.85 mmol) and diethyl azodicarboxylate (0.13 ml, 0.85 mmol). After stirring at room temperature for 2h the reaction was worked up as described in Example 1 to give the title compound as a colourless solid m.p. 195-197°C (methanol-diethyl ether).

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Abstract

Use of compounds of formula (I), in which p, q and r each independently represent an integer from 1 to 4; A is a bond, -CH=CH-, -C=C-, oxygen, sulphur or NR1, where R1 is hydrogen, C¿1-8?alkyl or phenylC1-4alkyl; n is 0 to 6, and m is 0 to 6, such that the length of the chain -(CH2)nA(CH2)m is at least two atoms; and Ar is aryl or heteroaryl, each of which may be optionally substituted; and pharmaceutically acceptable salts thereof, for the manufacture of a medicament for the treatment of disorders where a calcium channel antagonist is indicated. Novel compounds of formula (I), processes for preparing them and pharmaceutical compositions containing them are also described.

Description

AZABRICYCLIC COMPOUNDS AS CALCIUM CHANNEL ANTAGONISTS
The present invention relates to the use of known and novel azabicyclic derivatives in therapy, in particular as calcium channel antagonists, novel compounds pa: .S£» processes for their preparation, and pharmaceutical compositions containing them.
US Patent No.4,599,344 describes quinuclidines of the formula :
Figure imgf000003_0001
wherein Rj is inter alia hydrogen, R-2 is hydrogen or ALK-Z and R3 is hydrogen or ALK"-Z, where ALK is C2-4alkyl, ALK" is Cj^alkyl and Z is a mono- or- di-substituted phenyl ring. These compounds are said to be antiarrhythmic agents.
Ricciardi and Doukas (Heterocycles, Vol 24, No 4, p971, 1986) describe certain styrylquinuclidines, which are said to inhibit cholineacetyl-transferase in vitro.
German OLS 41 16582 describes azabicyclic compounds of the formula
Figure imgf000003_0002
wherein A, B and C independently represent -CH2- or a single bond; n is zero, 1 or 2; X is oxygen or sulphur and R is inter alia phenylalkyl, diphenylalkyl, heterocyclicalkyl, phenyl, diphenyl or a heterocycle, each of which may be optionally substituted. These compounds are said to be useful as muscaiinic antagonists.
EPA 497415 describes 3-(substituted phenoxy and substituted phenylthio)quinuclidines, wherein the phenyl substitutent is selected from inter alia lower alkoxy, lower aralkyloxy, halogen, NO2, CF3, CN and NRjR2, which compounds are said to be muscarinic agonists. e have now found that certain substituted azabicyclic derivatives, including some of the above compounds, exhibit activity as calcium channel antagonists. They are thus of potential use in the treatment of disorders where calcium channel blockade is indicated, in particular disorders related to an accumulation of calcium in the brain cells of mammals.
The present invention therefore provides, in a -first aspect, the use of a compound of formula (I):
Figure imgf000004_0001
Formula (I)
in which
p, q and r each independently represent an integer from 1 to 4; A is a bond, -CH=CH-, -C≡C-, oxygen, sulphur or NR , where R! is hydrogen, Cι_galkyl orphenylCι_4alkyl;
n is 0 to 6, and m is 0 to 6, such that the length of the chain -(CH2)nA(CH2)m is at least two atoms; and
Ar is aryl or heteroaryl, each of which may be optionally substituted;
or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment of disorders where a calcium channel antagonist is indicated.
The H atom is shown on the bridgehead carbon atom to make clear that the (CH2)nA(CH2)mAr chain cannot be attached at this position.
The compounds of formula (I) have been found to exhibit high calcium influx blocking activity for example in neurons. As such the compounds are expected to be of use in therapy, particularly in treating conditions and diseases related to (e.g. caused or exacerbated by) an accumulation of calcium in the brain cells of mammals, in particular humans. For example, the compounds are expected to be of use in the treatment of anoxia, ischaemia including for example stroke, migraine, epilepsy, traumatic head injury, AEDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age- related memory disorders, and drug addiction withdrawal such as ethanol addiction withdrawal.
In a further aspect of the invention there is also provided a method of treatment of conditions or diseases related to (e.g. caused or exacerbated by) the accumulation of calcium in the brain cells of mammals which comprises administering to a subject in need thereof an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof. Thus, for example, the present invention provides a method of treatment of anoxia, ischaemia including for example stroke, migraine, epilepsy, traumatic head injury, AIDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age- related memory disorders, and drug addiction withdrawal such as ethanol addiction withdrawal, which comprises administering to a subject in need thereof, an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
In the compounds of formula (I) p and r are preferably independently 2 or 3; most preferably both are 2.
q is preferably 1 or 2.
The values of m and n should be chosen such that the length of the chain (CH2)nA(CH2)m is at least 2 atoms. In general the length of the chain -(CH2)nA(CH2)m is from 2 to 6 e.g. 2 to 5 atoms. Preferred values for n and m depend on the group A. Thus for example when A is oxygen the sum of n+m is preferably from 1 to 5, for example n may be 1, 2, 3 or 4 and m may be 0 or 1.
When A is a bond the sum of n+m should be at least 2, e.g. n+m may be 2 or 3. When A is CH=CH one or both of n and m may be zero, e.g. n may be zero or 1 and m may be zero.
A is preferably oxygen, a bond or -CH=CH-; most preferably A is oxygen.
When Ar represents aryl, suitable groups include, for example, unsaturated monocyclic and unsaturated or partially saturated bicyclic or tricyclic ring systems of up to 15 carbon atoms, such as, for example, phenyl, naphthyl, tetrahydronaphthyl, fluorene, fluorenone, dibenzosuberene and dibenzosuberenone. Preferred are optionally substituted phenyl rings. An aryl group may be substituted, for example, by a Cι_2alkylenedioxy group (e.g. phenyl substituted by a 3,4-methylenedioxy group) or by 1 to 3 substituents selected from halogen, C^alkoxy, nitro, SC^alkyl, NR2aR2b (in which R2a R2b can be independently H or Cι_4alkyl), OCF3, Cι_6alkyl, trifluoromethyl, CN, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylCι_4alkyl and optionally substituted phenylC^alkoxy.
Suitable optionally substituted phenylCι_4alkyl groups include, for example benzyl. Suitable optionally substituted phenylCι_4alkoxy groups include, for example benzyloxy groups.
Suitable substituents for said optionally substituted phenyl, phenoxy, phenylC^alkyl and phenylCι_4alkoxy groups include for example halogen, Cj^alkyl, Cj^alkoxy, nitro and trifluoromethyl groups.
Preferably the aryl group is a phenyl ring substituted by one or two substituents, in particular, by a phenyl; phenyl(Cι_4)alkyl, e.g. benzyl or phenethyl; phenoxy; or phenylCι_4alkoxy group; which groups may themselves be optionally substitued by halo, e.g. chloro.
When Ar represents heteroaryl suitable groups include, for example, unsaturated or partially saturated bicyclic and tricyclic ring systems containing at least one heteroatom. A bicyclic ring system preferably contains 8 to 10 ring members, such as quinolinyl, tetrahydroquinolinyl or benzofuranyl. A tricyclic ring system preferably contains from 11 to 15 ring members, and most preferably has the structure :
Figure imgf000006_0001
wherein Y1 represents Y(C ._2)t, Y is O, S or NR^ (where R^ is hydrogen or Ci^alkyl), Z is (CH2)S or -CH=CH-, s is 0, 1 or 2 and t is 0 or 1 or is a corresponding dehydro ring system. Examples of tricyclic heteroaryl groups include dibenzofuranyl, dibenzothienyl, carbazole, N-methylcarbazole, acridine and dibenzoxepine. The heteroaryl ring can be linked to the remainder of formula (I) via any suitable ring atom.
Suitable substituents for said heteroaryl rings include, for example, 1 to 3 substituents selected from halogen, trifluoromethyl, Cj.4alkyl, Cι_4alkoxy, phenyl, phenylCj^alkyl and phenylCχ_4alkoxy.
Alkyl groups present in the compounds of formula (I), alone or as part of another group, can be straight or branched. Thus a Cj^alkyl group may be for example methyl, ethyl, n-propyl, n-butyl or any branched isomer thereof such as isopropyl or t-butyl.
It will be appreciated that for use in medicine a salt of a compound (I) should be pharmaceutically acceptable. Examples of pharmaceutically acceptable salts include inorganic and organic acid addition salts such as hydrochloride, hydrobromide, sulphate, phosphate, acetate, fumarate, maleate, citrate, lactate, tartrate, oxalate, methanesulphonate or similar pharmaceutically acceptable inorganic or organic acid addition salts. Other non- pharmaceutically acceptable salts may be used for example in the isolation of a final product and are included within the scope of this invention.
The invention also provides novel compounds of formula (IA) :
Figure imgf000007_0001
Formula (IA)
in which
p, q and r each independently represent an integer from 1 to 4; n is 0 to 6; m is 0 to 6, and either
A is -C≡C- or NRl, where R* is hydrogen, Cj.galkyl or phenylCj_4alkyl; in which case Ar represents the group Ar as hereinbefore defined;
or A is a bond, in which case Ar* represents the group Ar as hereinbefore defined with the proviso that when each of p, q and r is 2 and Ar is phenyl substituted by one or two groups selected from halogen, Cι_4alkoxy, nitro, cyano or amino, then the group -(CH2)nA(CH2)m is not Cj^alkyl α to the quinuclidine nitrogen atom or C2-4alkyl β to the quinuclidine nitrogen atom, or A is -CH=CH- in which case Ar* represents the group Ar as hereinbefore defined with the proviso that when each of p, q and r is 2; n and m are both zero and Ar is mono- or di-chlσrophenyl, the group -(CH2)nA(CH2)m is not β to the quinuclidine nitrogen atom.
or A is oxygen or sulphur in which case Ar^ represents a group Ar2 which is phenyl substituted by a Cι_2alkylenedioxy group or by 1 to 3 substituents selected from SCι_4alkyl, OCF3, Q^ optionally substituted phenoxy, optionally substituted phenylCι_4alkyl and optionally substituted phenylCι_4alkoxy; or Ar2 is
an optionally substituted bicyclic or tricyclic aryl group of up to 15 carbon atoms;
an optionally substituted benzofuranyl group; or an optionally substituted tricyclic heteroaryl group;
and salts thereof.
Suitable substituents for said optionally substituted phenoxy, phenylC^alkyl and phenylCι_4alkoxy groups are as hereinbefore defined.
Bicyclic and tricyclic aryl and heteroaryl groups for Ar* and Ar2 include those defined hereinbefore for the group Ar.
In the compounds of formula (IA), p and r are preferably 2 or 3; q is preferably 1 or 2.
A is preferably O, -CH=CH- or a bond, n is preferably zero, 1 or 2; m is preferably zero or 1; Arl is preferably Ar2 as defined above, or when A is -CH=CH or a bond Ar may also represent phenyl substituted by an optionally substituted phenyl group.
A bicyclic aryl group is preferably naphthyl.
A bicyclic heteroaryl group is preferably benzofuranyl.
A tricyclic heteroaryl group is preferably dibenzofuranyl. A particular group of compounds according to the invention is that represented by formula (IB)
Figure imgf000009_0001
Formula (IB)
wherein p, q, r, n, m and A are as defined for formula (IA) and R^ represents optionally substituted phenoxy, optionally substituted phenylCι_4alkyl or optionally substituted phenylCι_4alkoxy, or R^ represents a fused benzene ring; and salts thereof.
Preferred meanings for p, q, r, n, m, and A are as described for formula (IA).
Most preferably A represents oxygen.
It will be appreciated that when R^ represents a fused benzene
4 ring the group — P " is a naphthyl group.
R preferably represents benzyl, benzyloxy or phenoxy, or is a fused benzene ring.
Another group of compounds according to the invention is that of formula (IC)
Figure imgf000009_0002
Formula (IC)
wherein p, q, r, n, m and A are as defined for formula (IA) and Y - and Z are as hereinbefore defined for formula (I); and salts thereof. Most preferably Y* is oxygen and Z is a bond.
Particular compounds of the invention include:
(±)3-(3,4-dichlorophenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(4-benzyloxyphenoxymethyl)- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(4-benzylphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(2-phenylphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(4-tert-butylphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(l-naphthyloxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride,
(±)3-(2-dibenzofuranyloxymethyl)- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(5-isoquinolinyloxy)methyl)- l-azabicyclo[2.2.2]octane hydrochloride, (±) endo-3-(4-benzylphenoxymethyl)-l-azabicyclo[2.2.1]heptane hydrochloride, (±) endo-3-(4-benzyloxyphenoxymethyl)- l-azabicyclo[2.2. l]heptane hydrochloride, (±) exo-3-(4-benzylphenoxymethyl)- l-azabicyclo[2.2. l]heptane hydrochloride, (±) exo-3-(4-benzyloxyphenoxymethyl)-l-azabicyclo[2.2.1]heptane hydrochloride, (±) E-3-[2-(l-naphthyl)ethenyl]-l-azabicyclo[2.2.2]octane hydrochloride, (±)E-3-[2-(4-biphenyl)ethenyl]- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[2-(l-naphthyl)ethyl]- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[2-(4-biphenyl)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride,
(±)E-3-[3-(l-naphthyl)prop-2-enyl]-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[3-(l-naphthyl)propyl]- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[2-(2-dibenzofuranyloxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[2-(4-benzyloxyphenoxy)ethyl]- l-azabicyclo[2.2.2]octane hydrochloride, (±)3-[2-(4-benzylphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride, (±)3-(4-phenoxyphenoxymethyl)- l-azabicyclo[2.2.2]octane hydrochloride,
(±) 3-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride,
(+) 3-[4-(2-dibenzofuranyloxy)butyl]-l-azabicyclo[2.2.2]octane hydrochloride,
(±) 3-[4-(4-phenoxyphenoxy)butyl]-l-azabicyclo[2.2.2]octane hydrochloride, (±) 3-[3-(4-phenoxyphenoxy)propyl]-l-azabicyclo[2.2.2]octane hydrochloride,
C±) 3-[2-[4-(2-phenylethyl)phenoxy]ethyl]-l-azabicycIo [2.2.2]octane hydrochloride,
(±) 3-[2-[4-[2-(4-chlorophenyl)ethyl]phenoxy]ethyl]-l-azabicyclo[2.2.2]octane hydrochloride,
(+) 3-[2-[5-(2-phenyl)benzo[b]furanyloxy]ethyl]-l-azabicyclo[2.2.2]octane hydrochloride, (+) 2-[2-(4-benzylphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride, (+) 2-[2-(4-benzyloxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (+) 2-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride, and (+) 4-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[3.3.1]nonane hydrochloride.
It will be appreciated that the compounds of formula (I) may contain one or more asymmetric centres. Such compounds will exist as optical isomers (enantiomers). Both the pure enantiomers, racemic mixtures (50% of each enantiomer) and unequal mixtures of the two are included within the scope of the invention. Further, all diastereomeric forms possible (pure enantiomers and mixtures thereof) are within the scope of the invention. In addition, when A represents -CH=CH- the compounds will exist as geometric isomers, and the invention encompasses all such isomers and mixtures thereof.
In compounds of formula (I) having two asymmetric centres the stereochemical configuration in which the group -(CH2)nA(CH2)mAr and the (CH2)q bridge are on the same side of the plane of the molecule which contains both bridgehead atoms and the ring carbon bonded to the group -(CH2)nA(CH2)mAr will herein be referred to as the exo configuration. Similarly the configuration of compounds in which the group -(CH2)nA(CH2)mAr and the bridge (CH2)q are on opposite sides of the above-mentioned plane will herein be referred to as the eπdo configuration. Both configurations are within the scope of this invention.
The compounds of the present invention can be prepared by processes analogous to those known in the art. The present invention therefore provides in a further aspect, a process for the preparation of a compound of formula (I) which comprises:
(a)for compounds of formula (I) in which A is O, S or NR , reaction of a compound of formula (II):
Formula (II) in which p, q, r and n are as described for formula (I) and A is O, S or NRl, with a compound of formula L(CH2)mAr in which m and Ar are as described for formula (I), and L is a leaving group;
(b) for compounds of formula (I) in which A is O, S or NRl, reaction of a compound of formula (πi):
Figure imgf000012_0001
Formula (HI)
in which p, q, r and n are as described for formula (T) and L* is a group displaceable by a nucleophile, with a compound of formula HA^(CH2)mAr where m and Ar are as described for formula (I) and A 1 is as described for formula (II); or
(c) for compounds of formula (I) in which A is NR*, reduction of a compound of formula (IV) :
Figure imgf000012_0002
Formula ON)
in which R^ represents the group
-(CH2)nΝ(R1)C(O)(CH2)m-iAr or
Figure imgf000012_0003
and p, q, r, n, m, and Ar are as described for formula (I);
(d) for compounds of formula ( ) in which A is a bond, reaction of a compound of formula (V) :
Figure imgf000013_0001
Formula (V)
(wherein L p, q, r, m and n are as hereinbefore defined).
with a compound of formula X Ar in which Ar is as described for formula (I), and X* is an alkali metal;
(e) For compounds wherein A is -CH=CH- reaction of a compound of formula (VI)
Figure imgf000013_0002
Formula (VI)
(wherein n, p, q and r are as hereinbefore defined) with a reagent serving to introduce the group Ar,
(f) Interconversion of one compound of formula (I) to a different compound of formula (I) e.g. the reduction of a compound wherein A is -CH=CH- to a compound wherein A is -CH2CH2-;
and optionally thereafter forming a salt.
In process (a) the reaction between a compound of formula (13) and a compound
L(CH2)mAr can take place under conditions which depend on the nature of the group L and the value of m. For example, when L is halogen or a sulphonic acid residue such as a tosylate or mesylate and m is other than zero, the reaction is carried out under standard conditions in a solvent, optionally in the presence of a base. When a fluoro-substituted aryl compound F-Ar is employed in process (a) (to prepare compounds where m is zero), the reaction is effected in the presence of a strong base such as sodium hydride, and in an inert organic solvent such as dimethylformamide. Preferably the aryl group is substituted by an activating group such as CF3 or NO2. If necesary, the azabicyclic nitrogen atom may be protected during the reaction by methods well known in the art, e.g. by prior formation of a quaternary derivative such as an N-benzyl derivative. Protection may also be effected by formation of a borane (BH3) complex. It will be appreciated that the N- protecting group should be chosen such that it can be removed without affecting other moieties in the molecule. Thus for example a benzyl protecting group may not be appropriate when the side chain (CH2)nA(CH2)mAr also contains a benzyl moiety such as a benzyloxy group. In general, N-protection is preferred when the leaving group L represents halogen, e.g. bromine, but when L is a sulphonic acid residue e.g. a tosylate, N- protection may not be necessary.
The reaction between a compound of formula (El) and a compound of formula HAl(CH2)mAr (process (b)) can take place under conditions which depend on the nature of i and A. For example when i is hydroxy, m is 0 and A^ is oxygen or sulphur the reaction is carried out in the presence of diethyl azodicarboxylate and triphenyl phosphine. Such a reaction is known as the Mitsunobu reaction (as described in Synthesis 1981, 1). Alternatively the leaving group l\ may be for example a halogen atom or a sulphonyloxy group eg. methane-sulphonyloxy or p-toluene sulphonyloxy in which case the compound (HI) may preferably be protected, e.g. as an acid salt, such as a hydrochloride salt
Reaction may be effected in the presence or absence of solvent, at a temperature in the range 0 to 200°C and may preferably be carried out in the presence of a base.
The reduction of a compound of formula (IV) according to process (d) can be effected by methods known in the art, for example using a reducing agent such as lithium aluminium hydride. Conveniently a compound of formula (IV) can be prepared (for example as described below) and reduced in a 'one-pot' reaction, without isolation of compound ON) itself.
The reaction between a compound of formula (N) in process (d) and a compound of formula X^Ar can take place under standard conditions known to those skilled in the art for the formation of carbon-carbon bonds.
Process (e) may be effected using a Wadsworth-Emmons reagent of the formula Ar(CH2)m+iP(O)(OAlk)2, such as a diethylphosphonate, or a Wittig reagent of the formula Ar(CH2) +ιPPh3X (where X is an anion) which compounds are available commercially or can be prepared by known methods. The reaction may be carried out in a solvent such as tetrahydrofuran optionally containing a crown ether such as 15-crown-5, or 18-crown-6, and in the presence of a strong base such as sodium hydride or potassium t-butoxide.
Interconversion reactions according to process (f) may be effected by methods well known in the art. Thus for example conversion of a compound (I) wherein A represents -CH=CH- into a compound (I) wherein A represents-CH2-CH2- may be effected by catalytic reduction.
Compounds of formula (II) wherein n is 1 to 6 and A* is oxygen may be prepared by reduction of the corresponding ester of formula (VII) :
Figure imgf000015_0001
Formula (VII)
wherein p, q and r are as hereinbefore defined and Alk is a Cj.βalkyl group e.g. ethyl. The reduction may be effected using a reducing agent such as lithium aluminium hydride in a solvent such as diethyl ether or tetrahydrofuran. Esters of formula (VII) wherein n is 1 are described for example in European Patent Applications 257,741 and 392,803 and by B.S. OrlekelM, J. Med Chem, 1991, 34, 2726 and Grob≤tal, Helv. Chim. Acta, 1957, 227, 2170. Esters wherein n is greater than 1 may be prepared by conversion of an ester wherein n is 1 to the corresponding N-methyl-N-methoxycarboxamide (e.g. by hydrolysis of the ester followed by reaction with thionyl chloride and N, O-dimethylhydroxylamine hydrochloride), which is then reduced to the aldehyde using diisobutylaluminium hydride. The aldehyde is further converted to the cyanomethyl derivative for example as described in EPA 363,085, followed by acid hydrolysis, and esterification to form an ester wherein n is 2. The sequence may be repeated to form higher homologues.
Homologation may also be effected by the method described in British Patent No. 1250534, starting with a compound (ϋ) wherein A is O and n is 1 and proceeding via the corresponding halomethyl and cyanomethyl derivatives to an ester of formula (VII) wherein n is 2 which may be reduced to an alcohol (II) wherein n is 2. A further method for the preparation of a compound of formula (II) wherein p, q, r and n each represent 2, A* is oxygen and the group (CH2)nAlH is α to the ring nitrogen atom involves cyclisation of a 4-piperidyl-but-2-enoic acid ester e.g. a methyl ester. The cyclisation is an intramolecular Michael reaction which may be carried out at elevated temperature in an inert solvent such as refluxing toluene. Methyl 4-piperidyl-but-2-enoate may be obtained from a suitable N-protected precursor such as methyl 4-(4-N-tert- butyloxycarbonylpiperidyl)-but-2-enoate (which may be prepared as described in EP 478363), using e.g. trifluoroacetic acid optionally in a solvent such as dichloromethane. Reduction e.g. with lithium aluminium hydride provides the above mentioned compound of formula (II).
Alternatively compounds of formula (II) may be prepared by reaction of an aldehyde of formula (VI) or a ketone of formula (Vm) :
Figure imgf000016_0001
Formula (VHI)
with triethylphosphonoacetate or triethylphosphonocrotonate, followed by catalytic hydrogenation to give an ethoxycarbonylalkyl derivative which is further reduced e.g. using lithium aluminium hydride, to the desired hydroxyalkyl compound. It will be appreciated that use of triethylphosphonoacetate results in a 2-carbon homologation whilst triethylphosphonocrotonate gives a 4-carbon homologation.
Compounds of formula (II) wherein n is zero may be prepared by reduction of a compound of formula (VII) e.g. using lithium aluminium hydride.
Ketones of formula (VHI) are commercially available or can be prepared by literature methods, generally via a Dieckmann cyclisation, (for example as described in EPA 94742).
Compounds of formula (II) wherein A is S or NR^ may be prepared from the corresponding hydroxy compound by standard methods, for example via formation of an alkyl halide followed by reaction with an appropriate amine or thiol. Compounds of formula (HI) wherein L* is OH can be prepared as described for compounds of formula (II), and compounds of formula (III) wherein i is a halogen atom, or a mesyloxy or tosyloxy group can be prepared from the corresponding alcohol in conventional manner.
The compounds of formula L(CH2)mAr and HAl(CH2)mAr may be prepared by standard methods well known in the art. For example compounds L(CH2) Ar wherein Ar is a substituted phenyl group and L is halo, e.g. bromo, may be prepared by Friedel-Crafts acylation of the corresponding substituted benzene derivative, using an appropriate acid chloride and catalysed by aluminium trichloride, followed by reduction in ≤ilji with triethylsilane.
When Ar represents a phenyl group substitued by benzyloxy compounds L(CH2)mAr may be prepared according to the following scheme :
PhCH2B 3rr
K-∞-
Figure imgf000017_0002
Figure imgf000017_0001
The starting materials are available commercially or may be prepared by standard methods, e.g. by reaction of 4-benzyloxybenzaldehyde with triethylphosphonocrotonate in a similar manner to that described for the preparation of compounds (II).
Compounds of formula (IV) wherein R^ is a group
-(CH2)nN(R1)C(O)(CH2)m-lAr can be prepared by reacting a compound of formula (II) wherein A represents NR* with an acylating agent corresponding to the group - (CH2)mAr, for example an acid chloride ClOC(CH2)m-iAr.
Compounds of formula (TV) wherein R^ is a group
-(CH2)n-lC(O)N(Rl)(CH2)mAr may be prepared for example by reaction of a corresponding compound wherein R^ represents -(CH2)n_iCO2H or an activated derivative thereof such as an acid halide, ester or anhydride, with an amine of formula HN(Rl)(CH2)m Ar. It will be appreciated that when the acid itself is employed, reaction with the amine should be effected in the presence of a coupling agent. The carboxylic acid may itself be prepared for example by oxidation of the corresponding alcohol, ie. a compound of formula (Q) wherein A* is oxygen. Compounds of formula (V) may be prepared in analogous manner to compounds of formula H); where necessary the chain length may be increased using methods well known in the art.
Compounds of formula (VI) may be prepared by conventional methods, for example the oxidation of a compound of formula (II) wherein A^ is oxygen, or conversion of the corresponding ester, e.g. by hydrolysis and subsequent reaction with thionyl chloride and N,O-dimethyl-hydroxylamine, followed by reduction of the resulting N-methyl- N-methoxy-carboxamide, using diisobutylaluminium hydride. Compounds of formula (VI) wherein n is 1 may be prepared from the corresponding compound wherein n is zero by various methods. For example the aldehyde wherein n is zero may be treated with (methoxymethyl) triphenylphosphonium chloride and potassium t-butoxide, followed by a strong acid, e.g. concentrated sulphuric acid, resulting in the aldehyde wherein n is 1. Alternatively the aldehyde may be converted to the corresponding cyanomethyl derivative as described in EPA 363085 followed by acid hydrolysis, conversion to the N-methyl- N-methoxycarboxamide and reduction. These procedures may also be used to form higher homologues.
When a compound of formula 0) is obtained as a mixture of enantiomers, these may be separated by conventional methods such as crystallisation in the presence of a resolving agent, or chromatography, for example using a chiral HPLC column.
For use in medicine, the compounds of the present invention are usually administered in a standard pharmaceutical composition. The present invention therefore provides in a further aspect pharmaceutical compositions comprising a novel compound of formula 0) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient
The compounds for use according to the invention may be administered by any convenient method for example by oral, parenteral, buccal, rectal or transdermal administration and the pharmaceutical compositions adapted accordingly.
The compounds of formula 0) and their pharmaceutically acceptable salts which are active when given orally can be formulated as liquids or solids, for example syrups, suspensions or emulsions, tablets, capsules and lozenges. A liquid formulation will generally consist of a suspension or solution of the compound or pharmaceutically acceptable salt in a suitable liquid carrier(s) for example, ethanol, glycerine, non-aqueous solvent, for example polyethylene glycol, oils, or water with a suspending agent, preservative, flavouring or colouring agent.
A composition in the form of a tablet can be prepared using any suitable pharmaceutical carrier(s) routinely used for preparing solid formulations. Examples of such carriers include magnesium stearate, starch, lactose, sucrose and cellulose.
A composition in the form of a capsule can be prepared using routine encapsulation procedures. For example, pellets containing the active ingredient can be prepared using standard carriers and then filled into a hard gelatin capsule; alternatively, a dispersion or suspension can be prepared using any suitable pharmaceutical caπier(s), for example aqueous gums, celluloses, silicates or oils and the dispersion or suspension then filled into a soft gelatin capsule.
Compounds for use according to the invention may also be administered parenterally, by bolus injection or continuous infusion. Typical parenteral compositions consist of a solution or suspension of the compound or pharmaceutically acceptable salt in a sterile aqueous carrier or parenterally acceptable oil, for example polyethylene glycol, polyvinyl pyrrolidone, lecithin, arachis oil or sesame oil. Alternatively, the solution can be lyophilised and then reconstituted with a suitable solvent just prior to administration.
Both liquid and solid compositions may contain other excipients known in the pharmaceutical art, such as cyclodextrins.
Preferably the composition is in unit dose form such as a tablet, capsule or ampoule.
Each dosage unit for oral administration contains preferably from 1 to 250 mg (and for parenteral administration contains preferably from 0.1 to 60 mg) of a compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base.
The daily dosage regimen for an adult patient may be, for example, an oral dose of between 1 mg and 500 mg, preferably between 1 mg and 250 mg, eg. 5 to 200 mg or an intravenous, subcutaneous, or intramuscular dose of between 0.1 mg and 100 mg, preferably between 0.1 mg and 60 mg, eg. 1 to 40 mg of the compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base, the compound being administered 1 to 4 times per day. Alternatively the compounds of the invention may be administered by continuous intravenous infusion, preferably at a dose of up to 400 mg per day. Thus the total daily dosage by oral administration will be in the range 1 to 2000 mg and the total daily dosage by parenteral administration will be in the range 0.1 to 400 mg. Suitably the compounds will be administered for a period of continuous therapy, for example for a week or more.
BIOLOGICAL DATA
Ca2+ Current Measurement
Cell preparations
Sensory neurons from dorsal root ganglia were dissociated from 1 day old rat pups (Forda et al, Developmental Brain Research, 22 (1985), 55-65). Cells were plated out onto glass coverslips and used within 3 days to permit effective voltage clamp of Ca2+ currents.
Solutions
The pipette (internal solution) contained in mM: CsCl, 130; HEPES, 10; EGTA, 10; MgCL2, 4; ATP, 2; buffered to pH 7.2 with CsOH. Cells were bathed in a normal Tyrodes solution before establishment of whole cell recording when the bathing solution was changed to one allowing isolation of Ca2+ currents. The external solution for recording Ca2+ channel currents contained in mM: BaCL2, 10; TEA-C1, 130; glucose, 10; HEPES, 10; MgCL2, 1; buffered to pH 7.3 with TEA-OH. Barium was used as the charge carrier as this assists in current isolation and calcium dependent inactivation of current is avoided. Compounds were dissolved in DMSO to make a 20 mM stock solution. At the drug concentration used the vehicle (0.1%) had no significant effect on Ca2+ currents. All experiments were performed at 21 to 24°C. Whole cell currents were recorded using List EPC-7 amplifiers and stored, digitised for later analysis using PC based software similar to that described previously (Benham & Tsien, Journal of Physiology (1988), 404, 767-784).
Ca2+ currents
Peak voltage gated Ca2+ channel currents of up to 10 nA from dorsal root ganglion neurons were recorded using 10 mM Ba2+ as charge carrier. Currents were evoked from a holding potential of -80 mV to a test potential of 0 or +10 mV every 15 seconds. This test potential was at the peak of the current voltage relationship and assessing block at this point reduced any errors due to drifting holding potential. Some cells showed slow rundown of current as is commonly seen when recording Ca2+ currents. The rundown rate was measured in control conditions and extrapolated through the time of drug application to derive a control value to relate the drug affected current to. Block by 20 mM drug was assessed 3 minutes after drug application.
Compounds of the invention gave percentage inhibition of plateau Ca2+ current in the range 28 - 99%.
PHARMACEUTICALFORMULATIONS
1. Formulation for intravenous infusion
Compound of formula 0) 0.1 - 60 mg
Sodium hydroxide/hydrochloric acid to pH ca 7 polyethylene glycol 0 - 30 ml propylene glycol 0 - 30 ml alcohol 0 - 10 ml water to 100 ml
2. Formulation for bolus injection
Compound of formula 0) 0.1 - 60 mg sodium hydroxide or hydrochloric acid to pH ca 7 polyethylene glycol 0 - 2.5 ml alcohol 0 - 2.5 ml water to 5 ml
A tonicity adjusting agent eg. sodium chloride, dextrose or mannitol may also be added.
3. Tablet for oral administration
mg/tablet Compotmd of formula 0) 25 lactose 153 starch 33 crospovidone 12 microcrystalline cellulose 30 magnesium stearate _2
255 The following non-limiting examples illustrate the preparation of compounds of formula 0) :
Preparation 1 (±)3-Hydroxymethyl-l-azabicyclo[2.2.2]octane
A solution of (±) methyl l-azabicyclo[2.2.2]oct-3-yl-carboxylate (B.S. Orlek et al., J. Med. Chem., 1991, 34, 2726) (llg, 65mmol) in dry diethyl ether (100ml) was added over 0.5h to a stirred, ice cold suspension of lithium aluminium hydride (4.94g, 130mmol) in dry diethyl ether (200ml), under nittogen. The reaction was allowed to warm to room temperature over 20 min and then quenched with wet ether followed by the minimum amount of water. The reaction was filtered and the precipitate was washed with 20% methanol in diethyl ether. The combined filtrate and washings were concentrated in vacua and the resulting clear oil was distilled to afford the title compound as a colourless oil (7.55g) b.p. 150°C, 0.4mmHg (Kugelrδhr) which solified on standing.
*H Nmr (CDCI3) 5 : 1.33-1.93 (6H, m), 2.27-2.52 (2H, m), 2.68-2.89 (4H, m), 2.94-3.07 (lH, m), 3.57 (2H, d, J=8Hz)
Preparation 2
(±) endo-3-hydroxymethyl-l-azabicycIo[2.2.1]heptane
The title compound was prepared in a similar manner to Preparation 1 from (±) endo ethyl l-azabicyclo[2.2.1]hept-3-ylcarboxylate (EP392803, Description 21) (2g, 11.8mmol) and lithium aluminium hydride (0.90g, 23.7mmol). This afforded the title compound as a white solid (1.22g) b.p. 150°C, 0.5mmHg O^ugelδhr).
*H Nmr (CDCI3) δ : 1.38-1.63 (2H, m) 1.83-2.00 (1H, m), 2.11-2.67 (5H, m), 2.75-3.03 (2H, m), 3.20-3.69 (3H, m).
Preparation 3
(±) exo-3-and endo-3-hydroxymethyl-l-azabicyclo[2.2.1]heptane
The title compound was prepared in a similar manner to Preparation 1 from (±) exo- and endo-ethyl l-azabicyclo[2.2. l]heρt-3-ylcarboxylate (EP392803, Description 22) (2g, ll.δmmol) and lithium aluminium hydride (0.90g, 23.7mmol). This afforded title compound as a clear oil (l.Olg) b.p. 150°C, 0.5mmHg (Kugelrδhr) consisting of a 6:1 mixture of exo and endo isomers. ^H Nmr (CDCI3) (Signals corresponding to the major exo- isomer) δ : 1.11-1.25 (IH, m), 1.53-1.71 (2H, m), 2.17-2.91 (7H, m) 3.28-3.51 (3H, m).
Preparation 4
(±)3-Formylmethyl-l-azabicyclo[2.2.2]octane
A suspension of potassium tert-butoxide (1.62g, 14.39mmol) in dry tetrahydrofuran (50ml), at -20°C, under nitrogen, was treated with (methoxymethyl)triphenylphosphonium chloride (4.93g, 14.39mmol) over 30 min. After stirring at -20°C for 30 min the reaction was treated with a solution of (±)l-azabicyclo[2.2.2]oct-3-ylcarboxaldehyde (EP363085, Description 32) (lg, 7.19mmol) in tetrahydrofuran (5ml). The reaction was stirred at - 20°C for lh, then quenched by the addition of 5N sulphuric acid (15ml). The separated aqueous layer was washed with chloroform (2x10ml), then cooled in ice and treated dropwise with concentrated sulphuric acid (3ml). After stirring for 1.5h at 0°C, the solution was basified with potassium carbonate, then extracted into chloroform (3x40ml). The combined organic extracts were dried over sodium sulphate then concentrated in vacua. The residue was taken up in diethyl ether, filtered, then concentrated in vacua and distilled to afford the title compound as a clear oil (0.42g) b.p. 175°C, 0.8mmHg (Kugelrδhr).
Preparation 5 (±)3-(2-HydroxyethyI)-l-azabicyclo[2.2.2]octane
The title compound was prepared in a similar manner to Preparation 1 from (±) 3- ethoxycarbonylmethyl-l-azabicyclo-[2.2.2]octane (EP 363085, Description 3), (8.72g, 44.3mmol) and lithium aluminium hydride (5.04g, 132mmol). This afforded the title compound as a clear oil (4.22g) b.p. 175°C, 0.2mmHg (Kugelrohr).
4ϊ Nmr (CDCI3) δ : 1.29-1.72 (8H, m), 2.30-2.41 (IH, m), 2.68-2.93 (5H, m), 3.00-3.13 (lHm), 3.55-3.66 (2H, t, J=7Hz).
Preparation 6 (±) 3-(3-EthoxycarbonylpropyI)-l-azabicycIo[2.2.2]octane
A solution of 3-quinuclidinone (l.Og, 8.0 mmol) and triethyl 4-phosphonocrotonate (2.50g, 10.0 mmol) in dry tetrahydrofuran (10 ml) was added over 15 min to a stirred ice cold suspension of sodium hydride (0.30g of an 80% dispersion in mineral oil, 10.0 mmol) in dry tetrahydrofuran (20 ml) containing 15-crown-5 (60 mg) under nitrogen. The reaction was allowed to warm up to room temperature. After 1.5 h further quantities of triethyl 4-phosphonocrotonate (0.625g, 2.5 mmol) and sodium hydride (0.075g of an 80% dispersion in mineral oil, 2.5 mmol) were added, and the mixture was left stirring overnight. The reaction was quenched with glacial acetic acid (1ml) and concentrated in vacuo. The residue was partitioned between aqueous saturated potassium carbonate (30 ml) and chloroform (30 ml). The aqueous phase was further extracted with chloroform (2x30 ml), and the combined organic extracts were dried over sodium sulphate and concentrated in vacuo. Treatment with ethereal hydrogen chloride afforded the hydrochloride salt (2.1g) which was dissolved in ethanol (40 ml) and hydrogenated over 10% Pd-C (0.5g) at atmospheric pressure for lh. After removal of the catalyst by filtration through kieselguhr the filtrate was concentrated in vacuo. The residue was partitioned between saturated aqueous potassium carbonate (25 ml) and chloroform (25 ml). The aqueous layer was extracted with chloroform (2x25ml) and the combined organic extracts were dried over sodium sulphate and concentrated in vacuo to give the title compound as an oil (1.95g) which was used in the next stage without purification.
*H Nmr (CDCI3) δ : 1.20-1.75 (13H, m), 2.30 (3H, m), 2.80 (4H, m), 3.08 (IH, m), 4.12 (2H, q, J=6Hz)
Preparation 7 (±) 3-(4-Hydroxybutyl)-l-azabicyclo[2.2.2]octane
The title compound was prepared in a similar manner to Preparation 1 from (+) 3- (3- ethoxycarbonylpropyl)-l-azabicyclo[2.2.2]octane (1.94g) and lithium aluminium hydride (1.21g, 32 mmol). This afforded the title compound as an oil (l.Og, 68% based on 3- quinuclidinone) which solidified on standing and was used in the next stage without purification.
-H Nmr (CDCl )δ: 1.22 - 1.78 (13H, m), 2.32 (IH, m), 2.77 (4H, m), 3.07 (IH, m), 3.62 (2H, t, J=6Hz)
Preparation 8 (±) 3-(2-Ethoxycarbonylethyl)-l-azabicyclo[2.2.2]octane
The title compound was prepared in a similar manner to Preparation 6 from (+) 1- azabicyclo[2.2.2]octan-3-yl carboxaldehyde (EP 363085, Description 32) (1.50g, 10.8 mmol), triethyl phosphonoacetate (2.78 ml, 14.0 mmol), sodium hydride (0.39g of an 80% dispersion in mineral oil, 13.0 mmol) and 15-crown-5 (O.lg). After lh at room temperature, the reaction was quenched with glacial acetic acid (1.5ml) and worked up as described in Preparation 6. Hydrogenation in ethanol (40 ml) over 10% Pd-C (0.5g) at atmospheric pressure afforded the title compound as an oil (1.97g, 86%) which was used in the next stage without purification.
!H Nmr (CDC1 ) δ: 1.28 (3H, t, J=6Hz), 1.30-1.80 (8H, m), 2.20-2.40 (4H, m), 2.80 (4H, m), 3.10 (2H, m), 4.12 (2H, q, J=6Hz).
Preparation 9
(±) 3-(3-HydroxypropyI)-l-azabicyclo[2.2.2]octane hydrochloride
The title compound was prepared in a similar manner to Preparation 1 from (+) 3-(2- ethoxycarbonylethyl)-l-azabicyclo[2.2.2]octane (1.97g, 9.34 mmol) and lithium aluminium hydride (1.06g, 27.9 mmol). Purification by flash chromatography on neutral alumina using 0-10% methanol in chloroform as eluant, followed by distillation afforded the title compound as an oil (0.46g, 30%) b.p. 180°C, 0.2 mmHg (Kugelrohr).
XH Nmr (CDCl3)δ: 1.28-1.78 (10H, m), 2.35(1H, m), 2.75 (4H, m), 2.90-3.12 (IH, m and IH, hr s), 3.60 (2H, t, J=6Hz).
Preparation 10 (±) 2-(2-MethoxycarbonylmethyI)-l-azabicyclo[2.2.2]octane
A solution of methyl 4-(4-N-t-butyloxycarbonylpϊperidinyl)-but-2-enoate (EP 478363) (5.0g, 17.67 mmol) in dry dichloromethane (50ml) was treated with trifluoroacetic acid (10ml) and the mixture was stirred at room temperature for 24h. The reaction was concentrated in vacuo, cooled in ice and treated with a saturated aqueous solution of potassium carbonate (75ml). After exhaustive extraction with chloroform the combined organic layers were dried over sodium sulphate and concentrated in vacuo. The residue was extracted into diethyl ether, and insoluble impurities removed by filtration. The filtrate was concentrated in vacuo. The residue was dissolved in dry toluene (200ml) and heated under reflux in a nitrogen atmosphere for 12h. The reaction was concentrated in vacuo and the residue was distilled to give the title compound as a colourless oil (2.8g, 88%) b.p. 135°C at
0.2 mm Hg (Kugelrohr). !H Nmr (CDCI3) δ: 1.10 (IH, m); 1.50 (4H, m); 1.80 (2H, m); 2.45 (IH, dd, J=15Hz and 7Hz); 2.60 (IH, dd, J= 15Hz and 7Hz); 2.73 (IH, m), 2.95 (3H, m); 3.30 (IH, m); 3.68 (3H, s).
Preparation 11
(±) 2-(2-Hydroxyethyl)-l-azabicyclo[2.2.2]octane
The title compound was prepared in a similar manner to Preparation 1 from (+) 2-(2- methoxycarbonyl-methyl)-l-azabicyclo [2.2.2] octane (2.1g, 11.48mmol) and lithium aluminium hydride ( 1.74g, 45.90mmol) employing a reaction time of 2h at room temperature. This afforded the title compound as a colourless solid (1.67g, 94%) b.p. 180°C at 0.1 mm Hg (Kugelrohr).
Preparation 12 4-[2-(4-Chlorophenyl)ethyI]phenol
A solution of 4-chloro-4 -hydroxystilbene (5.43g) in ethanol (80ml) was hydrogenated over 5% Pd-C (l.Og) at atmospheric pressure for lh. Catalyst was removed by filtration through kieselguhr. The filtrate was concentrated in vacuo and distilled to give the title compound as a colourless solid (4.66g, 85%) b.p. 250°C, 0.1 mm Hg (Kugelrohr)
Preparation 13 2-Phenyl-5-hydroxybenzo[b]furan
A solution of 2-phenyl-5-methoxybenzo[b]furan (K K Thomas and M M Bokadia, J Indian Chem. Soc. 1966, 43, 713) (0.5g, 2.23 mmol) in absolute chloroform (4 ml) was treated with trimethylsilyl iodide (0.44 ml, 3.09 mmol) and warmed at 50°C for 48h. A further quantity (0.22ml) of trimethylsilyl iodide was added during this period. The reaction mixture was diluted with methanol (20 ml), treated with brine (40 ml) and extracted into diethyl ether (2x40ml). The combined extracts were washed with aqueous sodium metabisulphite, followed by brine (40ml) and dried over sodium sulphate. After concentration in vacuo the residue was distilled to give the title compound as a colourless solid (0.41 g, 88%) b.p. 250°C, 0.1 mm Hg kugelrohr). Preparation 14 G 4-Ethoxycarbonylmethyl-l-azabicyclo[3J.l]nonane
To a solution of triethyl phosphonoacetate (2.62ml, 13.19mmol) in dry N, N-dimethyl- formamide (13ml) cooled to 0°C under nitrogen was added potassium t-butoxide (1.16g, 10.36mmol) portionwise over 30 min. After stirring at 0°C for 45 min the mixture was cooled to -10°C and treated dropwise with a solution of 1-azabicyclo [3.3.1]nonan-4-one (1.3g, 9.42 mmol) in dry N, N-dimethylformamide (7ml). The reaction was allowed to warm to room temperature and after 6 h quenched below 0°C with excess glacial acetic acid. The mixture was concentrated in vacuo and the residue was treated with 2M orthophosphoric acid (30ml), and washed exhaustively with diethyl ether. The aqueous layer was saturated with potassium carbonate and extracted into chloroform (3x30ml). The combined organic extracts were dried over sodium sulphate and concentrated in vacuo. The crude product was purified by flash chromatography on neutral aluminia using 0-2% methanol in chloroform as eluant. The major faster running component was hydrogenated in ethanol (25 ml) over 5% Pd-C (0.2g) at atmospheric pressure for 4h. The catalyst was removed by filtration through kieselguhr, and the filtrate was concentrated in vacuo. The residue was partitioned between aqueous saturated potassium carbonate (15ml) and chloroform (15ml). The aqueous phase was extracted with chloroform (2x15ml) and the combined organic layers were dried over sodium sulphate and concentrated in vacuo. Chromatography on silica using 2-15% methanol in chloroform as eluant afforded the title compound as a clear oil (0.19g).
Preparation 15 (±) 4-(2-Hydroxyethyl)-l-azabicyclo[3.3.1]nonane
The title compound was prepared in a similar manner to Prepartion 1 from (+) 4- ethoxycarbonylmethyl-1-azabicyclo [3.3.1] nonane (0.18g, 0.86mmol) and lithium aluminium hydride (65mg, 1.71mmol). This afforded the title compound as a clear oil (0.12g, 83%) b.p. 190°C, 0.2mmHg kugelrohr). Example 1
(±)3-(3,4-Dichlorophenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (El)
A solution of (±) 3-hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol) in dry tetrahydrofuran (40 ml), under nitrogen, was treated with 3,4-dichlorophenol (0.867g, 5.32mmol) in dry tetrahydrofuran (2 ml), then treated with triphenylphosphine (1.21g, 4.61mmol) in tetrahydrofuran (2 ml). Diethyl azodicarboxylate (0.80g, 4.61mmol) was added to the reaction over 0.5 h and the mixture was stirred overnight at room temperature. The reaction was concentrated in vacuo treated with saturated aqueous potassium carbonate (25ml), then extracted into chloroform (3x25ml). The combined organic extracts were dried over sodium sulphate, concentrated in vacuo and the residue chromatographed on neutral alumina in a gradient of 0-2% methanol in chloroform. The gum produced was converted to the HC1 salt, which was washed thoroughly with diethyl ether then crystallised to afford the title compound as a white solid (0.78g) m.p. 194- 197°C (from methanol - diethyl ether).
IH Nmr (DMSO-d6) δ : 1.61-2.12 (5H, m), 2.38-2.54 (IH, m), 2.83-2.94 (IH, m), 3.04-3.45 (5H, m), 4.10 (2H, d, J=Hz), 6.98 (IH, dd, J=4, 9Hz), 7.28 (IH, d, J=4Hz), 7.53 (IH, d, J=9Hz).
Example 2
(±)3-(4-Benzyloxyphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (E2)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (2g, 14.2mmol), 4-(benzyloxy)phenol (8.52g, 42.6mmol), triphenylphosphine (4.84g, 18.4mmol) and diethyl azodicarboxylate (3.21g, 18.4mmol). This afforded the title compound as a white solid (3g) m.p.205-207°C (from methanol-diethyl ether).
IH Nmr £>MSO-d6) δ : 1.64-2.13 (5H, m), 2.38-2.52 (IH, m), 2.83-2.91 (IH, m), 3.07-3.46 (5H, m), 3.98 (2H, d, J=8Hz), 5.05 (2H, s), 6.86-6.99 (4H, m), 7.28-7.46 (5H, m) Example 3
(±)3-(4-BenzyIphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (E3)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), , 4-hydroxydiphenylmethane (0.98g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded die title compound as a white solid (0.46g) m.p. 169- 171°C (methanol-diethyl ether).
IH Nmr φMSO-ds) δ : 1.60-2.12 (5H, m), 2.36-2.51 (IH, m), 2.80-2.92 (IH, m), 3.08-3.45 (5H, m), 3.85 (2H, s), 3.99 (2H, d, J=7Hz), 6.79-6.92 (2H, m), 7.07-7.31 (7H, m)
Example 4
(±)3-(2-Phenylphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (E4)
The title compound (E4) was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 2-phenylphenol (0.905g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound as a white solid (0.49g) m.p. 184-187°C (from methanol-diethyl ether).
!H Nmr φMSO-dg) δ : 1.64-2.11 (5H, m), 2.42-2.57 (IH, m), 2.95-3.54 (6H, m), 4.16 (2H, d, 7Hz), 7.09-7.62 (9H, m).
Example 5
(±)3-(4-tert-Butylphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (E5)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 4-tert-butylphenol (0.80g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound (E5) as a white solid (0.35g) m.p. 276- 279°C (from methanol-diethyl ether). !H Nmr φMSO-dg) δ : 1.24 (9H, s), 1.63-2.15 (5H, m), 2.39-2.53 (IH, m), 2.83-2.94 (IH, m), 3.08-3.47 (5H, m), 4.02 (2H, d, J=7Hz), 6.88 (2H, d, J=8Hz), 7.30 (2H, d, J=8Hz)
Example 6
(±)3-(l-NaphthyloxymethyI)-l-azabicyclo[2.2.2]octane hydrochloride (E6)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 1-naphthol (0.77g,
5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound as a white solid (0.18g) m.p.206-208°C (from methanol-diediyl ether).
*H Nmr φMSO-c ) δ : 1.60-1.72 (IH, m), 1.77-2.01 (3H, m), 2.11-2.20 (IH, m), 2.53- 2.66 (IH, m), 2.89-3.01, (IH, m), 3.05-3.32 (4H, m), 3.41-3.53 (IH, m), 4.18 (2H, d, J=7Hz), 6.95 (IH, d, J=7Hz), 7.29-7.52 (4H, m), 7.75-7.84 (IH, m), 8.02-8.10 (IH, m).
Example 7
(±)3-(2-DibenzofuranyloxymethyI)-l-azabicyclo[2.2.2]octane hydrochloride (E7)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 2-hydroxy-dibenzofuran (0.98g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and dietiiyl azodicarboxylate (0.81g, 4.61mmol). The crude product was purified on neutral alumina in a gradient of 0- 2% methanol in toluene. Pooling of fractions containing the faster running component afforded a gum which was treated with ethereal hydrogen chloride to give the title compound as a white solid (0.29g) m.p.246-247°C (from methanol-diethyl etiier).
iH Nmr ODMSO^ δ : 1.68-2.08 (4H, m), 2.13-2.19 (lH, m), 2.47-2.59 (lH, m), 2.92-3.00 IH, m), 3.11-3.49 (5H, m), 4.18 (2H, d, 8Hz), 7.13 (IH, dd, 3=2, 7Hz), 7.38 (IH, t, J=7Hz), 7.51 (IH, t J=7Hz), 7.52 (IH, d, J=7Hz), 7.56 (IH, d, J=7Hz), 7.77 (IH, d, J=2Hz), 8.12 (IH, d, J=7Hz) Example 8
(±)3-(5-IsoquinoIinyloxy)methyl)-l-azabicyclo[2.2.2]octane hydrochloride (E8)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 5-hydroxyisoquinoline (0.72g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and dietiiyl azodicarboxylate (0.8g, 4.61mmol). This afforded the title compound as a white solid (0.19g) m.p. 277-280°C (from methanol-diethyl ether).
*H Nmr φMSO-d^ δ : 1.73-2.18 (4H, m), 2.27-2.36 (IH, m), 2.71-2.86 (IH, m), 3.04-3.45 (5H, m), 3.55-3.70 (IH, m), 4.46 (2H, d, 7Hz), 7.74 (IH, d, J=7Hz), 8.02 (IH, t, J=7Hz), 8.16 (IH, d, J=7Hz), 8.56 (IH, d, J=6Hz), 8.74 (IH, d, J=6Hz), 9.92 (IH, s)
Example 9
(±) endo-3-(4-Benzylphenoxymethyl)-l-azabicy o[2.2.1]heptane hydrochloride (E9)
The title compound was prepared in a similar manner to Example 1 from (±)endo-3- hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-hydroxydiphenylmethane (1.09g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and diethyl azodicarboxylate (0.89g, 5.12mmol). This afforded the title compound as a white solid (0.77g) m.p. 153-156°C (from methanol-acetone-diediyl ether).
XH Nmr (DMSO- δ : 1.83-1.93 (2H, m), 2.74-2.95 (3H, m), 3.11-3.39 (4H, m),
3.45-3.53 (IH, m), 3.90 (2H, s), 3.99-4.11 (2H, s), 6.85-6.92 (2H, m), 7.12-7.32 (7H, m).
Example 10
(±) endo-3-(4-BeπzyloxyphenoxymethyI)-l-azabicyclo[2.2.1]heptane hydrochloride (E10)
The title compound was prepared in a similar manner to Example 1 from (±)endo-3- hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-benzyloxyphenol (1.18g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and diethyl azodicarboxylate (0.89g, 5.12mmol). This afforded the title compound as a white solid (0.3 lg) m.p. 156-158°C (from methanol-acetone-diethyl ether). 1H Nmr (CDCI3) δ : 1.99-2.16 (2H, m), 2.86-2.97 (2H, m), 3.07-3.25 (3H, m), 3.28-3.36 (IH, m), 3.52-3.62 (IH, m), 3.68-3.78 (IH, m), 3.93-3.99 (IH, m), 4.03-4.08 (IH, m), 5.04 (2H, m), 6.78-6.85 (2H), 6.87-6.94 (2H, m), 7.26-7.44 (5H, m).
Example 11
(±) exo-3-(4-Benzylphenoxymethyl)-l-azabicydo[2.2.1]heptane hydrochloride (Ell)
The tide compound was prepared in a similar manner to Example 1 from (±)exo- and endo-3-hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol),
4-hydroxydiphenylmethane (1.09g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and diethyl azodicarboxylate (0.89g, 5.12mmol). The crude product was chromatographed on silica in a gradient of 0-20% methanol in chloroform. Pooling of pure fractions containing the major faster running component gave a gum which was converted into the hydrochloride salt to afford the title compound as a white solid (0.5g) m.p. 145-148°C (from methanol-acetone-diethyl ether).
*H Nmr (DMSO-c ) δ : 1.62-1.72 (IH, m), 1.95-2.05 (IH, m), 2.32-2.42 (IH, m), 2.78-2.83 (IH, m), 2.93-3.08 (2H, m), 3.14-3.23 (IH, m), 3.26-3.43 (3H, m), 3.84-3.94 (3H, m), 3.97-4.03 (IH, m), 6.84-6.90 (2H, m), 7.12-7.32 (7H, m).
Example 12
(±) exo-3-(4-Benzyloxyphenoxymethyl)-l-azabicyclo[2.2.1]heptane hydrochloride (E12)
The title compound was prepared in a similar manner to Example 1 from (±)exo- and endo-3-hydroxymethyl-l-azabicyclo[2.2.1]heptane (0.5g, 3.94mmol), 4-benzyloxyphenol (1.18g, 5.91mmol), triphenylphosphine (1.34g, 5.12mmol) and dietiiyl azodicarboxylate (0.89g, 5.12mmol). The crude product was chromatographed on silica in a gradient of 5- 20% methanol in chloroform. Pooling of pure fractions containing the major faster running component gave a gum which was converted into the hydrochloride salt to afford the title compound as a white solid (0.29g) m.p. 156-158°C (from methanol-acetone- diediyl ether).
*H Nmr φMSO-dg) δ : 1.72-1.87 (IH, m), 2.05-2.12 (IH, m), 2.43-2.58 (IH, m), 2.93- 2.98 (IH, m), 3.06-3.50 (6H, m), 3.94-4.16 (2H, m), 5.20 (2H, m), 6.95-7.17 (4H, m), 7.42-7.65 (5H, m). Example 13
(±) E-3-[2-(l-Naphthyl)ethenyl]-l-azabicyclo[2.2.2]octane hydrochloride (E13)
A solution of l-azabicyclo[2.2.2]oct-3-yl carboxaldehyde (EP363085, Description 32) (lg, 7.19mmol) and dietiiyl 1-naphthylmethylphosphonate (2g, 7.19mmol) in tetrahydrofuran (10ml) was added over 10 min to an ice cold slurry of sodium hydride (0.216g of an 80% dispersion in mineral oil, 7.19mmol) and 15-crown-5 (60mg) in tetahydrofuran (20ml) under nitrogen (R. Baker et al., Synthesis, 1981, 117). The mixture was allowed to warm to room temperature and stirred for 2 h. The reaction was quenched by die addition of acetic acid (1ml), then concentrated in vacuo. The residue was treated with saturated aqueous potassium carbonate (25ml) then extracted into chloroform (3 x 25ml). The combined organic extracts were dried over sodium sulphate, concentrated in vacuo and die residue chromatographed on neutral alumina in a gradient of 0-2% methanol in chloroform. The gum produced was converted into the HC1 salt, which was washed tiiσroughly with dietiiyl ether then crystallised to afford the title compound as a white solid (1.4g) m.p. 196-198°C (from methanol-diediyl ether).
!H Nmr φMSO-ds) δ : 1.74-2.28 (5H, m), 3.00-3.74 (7H, m), 6.58 (IH, dd, 3=7, 15Hz), 7.50 (IH, d, J=15Hz), 7.55-8.12 (6H, m), 8.25-8.32 (IH, m).
Example 14
(±)E-3-[2-(4-BiphenyI)ethenyl]-l-azabicyclo[2.2.2]octane hydrochloride (E14)
The tide compound was prepared in a similar manner to Example 13 from 1- azabicyclo[2.2.2]oct-3-yl-carboxaldehyde (0.78g, 5.61mmol), dietiiyl 4-biphenylmethyl- phosphonate (1.70g, 5.61mmol), sodium hydride (0.17g of an 80% dispersion in mineral oil, 5.61mmol) and 15-crown-5 (60mg). This afforded the title compound as a white solid (1.3g) m.p. 289-290°C (from methanol-diethyl ether).
IH Nmr (DMSO-d^) δ : 1.57-1.69 (IH, m), 1.75-1.98 (4H, m), 2.75-2.84 (IH, m), 2.94- 3.29 (5H, m), 3.35-3.43 (IH, m), 6.39 (IH, dd, J=8, 16Hz), 6.52 (IH, d, J=16Hz), 7.22- 7.61 (9H, m). Example 15
(±)3-[2-(l-NaphthyI)ethyI]-l-azabicyclo[2.2.2]octane hydrochloride (E15)
A mixture of (±)E-3-[2-(l-naphthyl)ethenyl]-l-azabicyclo[2.2.2[octane hydrochloride (0.7g, 2.34mmol) and 10% Pd-C (70mg) in methanol (25ml) was stirred at room temperature for 2 h under an atmosphere of hydrogen. The reaction was filtered, then concentrated in vacuo. The residue was treated with saturated aqueous potassium carbonate (25ml) and extracted into chloroform (3 x 25ml). The combined organic extracts were dried over sodium sulphate then concentrated in vacuo. The gum produced was converted into the HC1 salt to afford the title compound as white solid (0.415g) m.p. 169-171°C (from acetone-diethyl ether).
*H Nmr pMSO-dg) δ : 1.63-2.13 (8H, m), 2.76-2.85 (IH, m), 2.97-3.25 (6H, m), 3.38- 3.47 (IH, m), 7.38-3.47 (IH, m), 7.38-7.59 (4H, m), 7.79 (IH, d, J=7Hz), 7.94 (IH, d, J=8Hz), 8.09 (IH, d, J=7Hz).
Example 16
(±)3-[2-(4-Biphenyl)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E16)
The tide compound was prepared in a similar manner to Example 15 from (±)E-3-[2-(4- Biphenyl)ethenyl]-l-azabicyclo[2.2.2]octane hydrochloride (E14) (0.65g, 2mmol) and 10%Pd-C (65mg). This afforded the title compound as a white solid (0.14g) m.p. 236- 238 C (from methanol-acetone-dietiiyl ether).
!H Nmr (DMSO-dg) δ : 1.52-1.91 (8H, m), 2.45-2.54 (2H, m), 2.62-2.72 (IH, m), 2.93- 3.14 (4H, m), 3.22-3.32 (IH, m), 7.18-7.26 (3H, m), 7.31-7.38 (2H, m), 7.45-7.56 (4H, m).
Example 17
(±)E-3-[3-(l-Naphthyl)prop-2-enyl]-l-azabicyclo[2.2.2]octane hydrochloride (E17)
The title compound was prepared in a similar manner to Example 13 from (±)3- formylmethyl-l-azabicyclo[2.2.2]octane (0.41g, 2.68mmol), diethyl 1-naphthylmethyl- phosphonate (0.75g, 2.68mmol), sodium hydride (80mg of an 80% dispersion in mineral oil, 2.68mmol) and 15-crown-5 (30mg). This afforded the title compound as a white solid (0.47g) m.p. 174-177°C (from methanol-acetone-diethyl ether).
*H Nmr (DMSO-d^) δ : 1.62-2.25 (6H, m), 2.35-2.54 (2H, m), 2.78-2.90 (IH, m), 3.01- 3.48 (5H, m), 6.24 (IH, dt, J=7, 15Hz), 7.32 (IH, d, J=15Hz), 7.43-7.68 (4H, m), 7.78- 7.96 (2H, m), 8.14-8.25 (IH, m).
Example 18
(±)3-[3-(l-Naphthyl)propyI]-l-azabicyclo[2.2.2]octane hydrochloride (E18)
The title compound was prepared in a similar manner to Example 15 from (±)E-3-[3-(l- Naphythyl)prop-2-enyl]-l-azabicyclo[2.2.2]octane hydrochloride (E17) (0.23g, 7.34mmol) and 10%Pd-C (20mg). This afforded die title compound as a white solid (0.16g) m.p.l55°C (dec) (from methanol-acetone-diethyl etiier).
*H Nmr (DMSO-d^) δ : 1.47-2.22 (10H, m), 2.73-2.92 (IH, m), 3.05-3.58 (7H, m), 7.42-7.74 (4H, m), 7.82-8.26 (3H, m).
Example 19
(±)3-[2-(2-Dibenzofuranyloxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E19)
The tide compound was prepared in a similar manner to Example 1 from (±)3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 2-hydroxydibenzofuran
(0.89g, 4.84mmol), triphenylphosphine (l.Olg, 4.19mmol) and diethyl azodicarboxylate (0.73g, 4.19mmol). This afforded the title compound as a white solid (0.62g m.p 235- 237 C (methanol-acetone-diethyl ether).
*H Nmr (DMSO-d6) δ : 1.62-2.06 (7H, m), 2.15-2.28 (IH, m), 2.80-2.94 (IH, m), 3.05- 3.52 (5H, m), 4.11 (2H, t, J=6Hz), 7.09 (lh, dd, J=2,8Hz), 7.35-7.79 (5H, m), 8.12 (lH,d, J=8Hz). Example 20
(±)3-[2-(4-Benzyloxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E20)
The tide compound was prepared in a similar manner to Example 1 from (±)3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 4-benzyloxyphenol (lg, 4.84mmol), triphenylphosphine (l.Olg, 4.19mmol) and dietiiyl azodicarboxylate (0.73g, 4.19mmol). This afforded the title compound as a white solid (0.5g) m.p.215-216°C (from methanol-acetone-diethyl ether).
!H Nmr (DMSO-d^ δ : 1.57-1.98 (7H, m), 2.04-2.21 (IH, m), 2.73-2.85 (IH, m), 3.00- 3.40 (5H, m), 3.89 (2H, t, J=6Hz), 5.01 (2H, s), 6.79-6.96 (4H, m), 7.24-7.43 (5H, m).
Example 21
(±)3-[2-(4-BenzyIphenoxy)ethyl]-l-azabicycIo[2.2.2]octane hydrochloride (E21)
The title compound was prepared in a similar manner to Example 1 from (±)3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23mmol), 4-hydroxydiphenylmethane (0.89g, 4.84mmol), triphenylphosphine (l.Olg, 4.19mmol), and dietiiyl azodicarboxylate (0.73g, 4.19mmol). This afforded the title compound as a white solid (0.69g) m.p 186- 188 C (from methanol-acetone-diethyl ether).
!H NmrODMSO-dg) δ : 1.68-2.10 (7H, m), 2.15-2.34 (IH, m), 2.83-2.98 (IH, m), 3.10- 3.58 (5H, m,), 3.95 (2H, s), 4.03 (2H, t, J=7Hz), 6.82-6.93 (2H, m), 7.17-7.42 (7H, m).
Example 22
(±)3-(4-Phenoxyphenoxymethyl)-l-azabicyclo[2.2.2]octane hydrochloride (E22)
The title compound was prepared in a similar manner to Example 1 from (±)3- hydroxymethyl-l-azabicyclo[2.2.2]octane (0.5g, 3.55mmol), 4-phenoxyphenol (0.99g, 5.32mmol), triphenylphosphine (1.21g, 4.61mmol) and diethyl azodicarboxylate (0.80g, 4.61mmol). This afforded the title compound as a white solid (0.59g) m.p 176-178°C (methanol-acetone-diediyl ether. iH Nmr φMSO-ds) δ : 1.62-2.03 (4H, m), 2.07-2.14 (IH, m), 2.40-2.55 (IH, m), 2.86- 2.96 (IH, m), 3.07-3.48 (5H, m), 4.05 (2H, d, J=7Hz), 6.98-7.11 (7H, m), 7.28-7.40 (2H, m).
Example 23
(±) 3-[2-(4-Phenoxyphenoxy)ethyI]-l-azabicycIo[2.2.2]octane hydrochloride (E23)
The title compound was prepared in a similar manner to Example 1 from (+) 3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.22mmol), 4-phenoxyphenol (0.90g, 4.84 mmol), triphenylphosphine (l.Og, 4.19 mmol) and diethyl azodicarboxylate 0.66 ml, 4.19 mmol). After stirring at room temperature for 2h, the reaction was concentrated in vacuo. The residue was extracted into diethyl etiier, and treated with ethereal hydrogen chloride. The resulting hydrochloride salt was washed with diethyl ether and recrystallised to give the title compound as a colourless solid (0.7g) m.p. 182-185°C (from methanol-acetone- diethyl ether).
IH Nmr (DMSO-d£) δ:1.70-2.13 (7H, m, overlapping signals), 2.28 (lH,m), 2.95 (IH, m), 3.12-3.55 (6H, m), 4.07(2H, t, J=7Hz), 6.94-7.20 (7H, m), 7.45(2H, t, J=7Hz)
Example 24
(±) 3-[4-(2-Dibenzofuranyloxy)butyI]-l-azabicycIo[2.2.2]octane hydrochloride (E24)
The title compound was prepared in a similar manner to Example 1 from (±) 3-(4- hydroxybutyl)-l-azabicyclo[2.2.2]octane (0.5g, 2.73 mmol), 2-hydroxydibenzofuran (0.75g, 4.09 mmol), triphenylphosphine (0.93g, 3.55 mmol) and diethyl azodicarboxylate (0.56 ml, 3.55 mmol). After stirring at room temperature for lh the reaction was concentrated in vacuo. The crude product was converted into the hydrochloride salt, washed with diethyl ether, then partitioned betwen saturated aqueous potassium carbonate (25 ml) and chloroform (25 ml). The aqueous layer was further extracted with chloroform (2x25 ml), and the combined organic extracts were dried over sodium sulphate and concentrated in vacuo. Hash chromatography on alumina using 0.5-2% methanol in toluene as eluant, followed by treatment with ethereal hydrogen chloride afforded the title compound as a colourless solid (0.3 Ig) m.p.242-244°C (from methanol-diethyl ether). *H Nmr φMSO-dό) δ: 1.25-2.10 (12H, m, overlapping signals), 2.69 (IH, m), 2.94-3.50 (5H, m, overlapping signals), 4.08 (2H, t, J=7Hz), 7.08 (IH, dd, J=7Hz, 2Hz), 7.28-7.78 (5H, m, overlapping signals), 8.13 (IH, d, J=7Hz).
Example 25
(±) 3-[4-(4-Phenoxyphenoxy)butyl]-l-azabicyclo[2.2.2]octane hydrochloride (E25)
The title compound was prepared in a similar manner to Example 1 from (+) 3-(4- hydroxybutyl)-l-azabicyclo [2.2.2]octane (0.5g, 2.73 mmol), 4-phenoxyphenol (0.76g, 4.09 mmol), triphenylphosphine (0.93g, 3.55 mmol) and diethyl azodicarboxylate (0.56ml, 3.55 mmol). After stirring at room temperature for lh the reaction was worked up as described in Example 24. Purification by chromatography on neutral alumina using 0-2% methanol in chloroform as eluant, followed by treatment with ethereal hydrogen chloride afforded the title compound as a colourless solid (0.35g) m.p. 151-153°C (from methanol-dietiiyl ether).
!H Nmr φMSO-d^) δ: 1.35-2.16 (12H, m, overlapping signals), 2.78 (IH, m), 3.10-3.60 (5H, m, overlapping signals), 4.03 (2H, t, J=7Hz), 6.89-7.22 (7H, m), 7.43 (2H, m).
Example 26
(±) 3-[3-(4-Phenoxyphenoxy)propyI]-l-azabicyclo[2.2.2]octane hydrochloride (E26)
The title compound was prepared in a similar manner to Example 1 from (±)3-(3- hydroxypropyl)-l-azabicyclo[2.2.2]octane (0.45g, 2.66 mmol), 4-phenoxyphenol (0.74g, 3.98 mmol), triphenylphosphine (0.91g, 3.47 mmol) and diethyl azodicarboxylate (0.55 ml, 3.47 mmol). After stirring at room temperature for lh the reaction was worked up as described in Example 24. Purification by chromatography on neutral alumina using 0-2% methanol in chloroform as eluant, followed by treatment with ethereal hydrogen chloride afforded the title compound as a colourless solid (0.7g) m.p. 149-151°C (from methanol- acetone-dietiiyl ether).
!H Nmr φMSO-d ) δ: 1.54-2.20 (10H, m, overlapping signals), 2.80 (IH, m), 3.10-3.60 (5H, m, overlapping signals), 4.05 (2H, t, J=7Hz), 6.90-7.28 (7H, m), 7.43 (2H, t, J=8Hz) Example 27
(±) 3-[2-[4-(2-Phenylethyl)phenoxy]ethyl]-l-azabicycIo [2.2.2]octane hydrochloride
(E27)
The title compound was prepared in a similar manner to Example 1 from (±) 3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.23 mmol), trans 4-hydroxystilbene (0.95g, 4.84 mmol), triphenylphosphine (l.lg, 4.19 mmol) and diethyl azodicarboxylate (0.66 ml, 4.19 mmol). After stirring at room temperature for 1.5h the reaction was concentrated in vacuo. The residue was extracted into diethyl ether and treated with ethereal hydrogen chloride to give the hydrochloride salt which was washed with diethyl ether. A solution of this salt in ethanol (40 ml) was hydrogenated over 10% Pd-C (0.25g) at atmospheric pressure for 4h. After removal of the catalyst by filtration through Jrieselguhr, the filtrate was concentrated in vacuo. The residue was partitioned between saturated aqueous potassium carbonate (30 ml) and chloroform (25 ml). The aqueous phase was further extracted with chloroform (2x25 ml), and the combined organic extracts were dried over sodium sulphate and concentrated in vacuo. Purification by chromatography on neutral alumina using 0-2% methanol in chloroform as eluant afforded an oil which was treated with ethereal hydrogen chloride to give the title compound as a colourless solid (0.67g) m.p.210-212°C (from methanol-acetone-diethyl ether)-
iH Nmr (DMSO-dβ) δ: 1.55-2.05 (7H, m), 2.16 (IH, m), 2.82 (4H, m), 3.15 (4H, m), 3.38 (2H, m), 3.94 (2H, t, J=7Hz), 6.82 (2H, t, J=8Hz), 7.03-7.36 (7H, m).
Example 28
(±) 3-[2-[4-[2-(4-Chlorophenyl)ethyl]phenoxy]ethyI]-l-azabicyclo[2.2^]octane hydrochloride (E28)
The title compound was prepared in a similar manner to Example 1 from (+) 3-(2- hydroxyethylH-azabicyclo [2.2.2]octane (0.5g, 3.22 mmol), 4-[2-(4- chlσrophenyl)ethyl]phenol (1.13g, 4.86 mmol), triphenylphosphine (1.10g, 4.20 mmol) and diethyl azodicarboxylate (0.66 ml, 4.20 mmol). The reaction was worked up as described in Example 24. Purification by chromatography on neutral alumina using 0-2% methanol in chloroform as eluant followed by treatment with ethereal hydrogen chloride afforded the title compound as a colourless solid (0.56 g) m.p.220-222°C (from methanol-acetone-diethyl ether). H Nmr (DMSO-dό) δ: 1.55-2.00 (7H, m), 2.16 (IH, m), 2.82 (4H, m), 3.15 (4H, m), 3.37 (2H, m), 3.95 (2H, t, J=7Hz), 6.82 (2H, d, J=7Hz), 7.10 (2H, d, J=7Hz), 7.22 (2H, d, J=7Hz), 7.30 (2H, d, J=7Hz)
Example 29
(±) 3-[2-[5-(2-Phenyl)benzo[b]furanyloxy]ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E29)
The title compound was prepared in a similar manner to Example 1 from (+) 3-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.25g, 1.61 mmol), 5-hydroxy-2- phenylbenzo[b]furan (0.48g, 2.42 mmol), triphenylphosphine (0.59g, 2.25 mmol) and diethyl azodicarboxylate (0.36ml, 2.25 mmol). The reaction was worked up as described in Example 24. Purification by chromatography on neutral alumina using 0-2% methanol in chloroform as eluant followed by treatment with ethereal hydrogen chloride afforded the title compound as a colourless solid (0.35g), m.p. 266-267°C (from methanol-acetone- diethyl etiier).
*H Nmr £>MSO-d6) δ: 1.70-2.15 (7H, m), 2.30 (IH, m), 2.95 (IH, m), 3.14-3.62 (5H, m), 4.13 (2H, t, J=7Hz), 7.00 (IH, dd, J=7Hz, 2Hz), 7.27 (IH, d, J=2Hz), 7.40-7.68 (5H, m), 8.00 (2H, d, J=7Hz).
Example 30
(±) 2-[2-(4-Benzylphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E30)
The title compound was prepared in a similar manner to Example 1 from (±) 2-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (23mg, 0.15 mmol), 4-hydroxydiphenylmethane (41mg, 0.22 mmol), triphenylphosphine (59 mg, 0.22 mmol) and diethyl azodicarboxylate (39 mg, 0.22 mmol). After stirring at room temperature for 6h the reaction mixture was concentrated in vacuo. The residue was partitioned between water (5 ml) and chloroform (5ml) and the pH of the aqueous phase was adjusted to 12 with potassium carbonate. After further extraction with chloroform (3x5ml) the combined organic layers were dried over sodium sulphate and concentrated in vacuo. Chromatography on neutral alumina using 0- 5% ethanol in chloroform as eluant, followed by tteatment with ethereal hydrogen chloride afforded the hydrochloride salt which was washed with diethyl ether and recrystallised to give the title compound as a colourless solid (34 mg) m.p. 177-178.5°C (from acetone- diethyl ether). iH Nmr φMSO-ctø δ: 1.50 (IH, m), 1.73 (4H, ), 1.95-2.13 (3H, m), 2.32 (IH, m), 3.07-3.40 (4H, m), 3.57 (IH, m), 3.87 (2H, s), 4.05 (IH, m), 6.86 (2H, d, J=7Hz), 7.10- 7.30 (7H, m).
Example 31
(±) 2-[2-(4-Benzyloxyphenoxy)ethyI]-l-azabicyclo[2.2.2]octane hydrochloride (E31)
The tide compound was prepared in a similar manner to Example 30 from (±) 2-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.22mmol), 4-benzyloxyphenol (0.97g, 4.84mmol), triphenylphosphine (1.27g, 4.84mmol) and diethyl azodicarboxylate (0.76ml, 4.84mmol). This afforded the tide compound as a colourless solid (0.69g) m.p.238- 240°C (from acetone-diethyl ether).
iHNmr (DMSO-d^) δ: 1.70 (IH, m), 1.96 (4H, m), 2.19 (3H, m), 2.50 (IH, m), 3.28 (IH, m), 3.45 (3H, m), 3.74 (IH, m), 4.19 (2H, m), 5.22 (2H, s), 7.10 (4H, q, J=9Hz), 7.58 (5H, m), 10.47 (IH, br.s).
Example 32
(±) 2-[2-(4-Phenoxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane hydrochloride (E32)
The title compound was prepared in a similar manner to Example 30 from (+) 2-(2- hydroxyethyl)-l-azabicyclo[2.2.2]octane (0.5g, 3.22mmol), 4-phenoxyphenol (0.90g, 4.84mmol), triphenylphosphine (1.27g, 4.84mmol) and diethyl azodicarboxylate (0.76ml, 4.84mmol). This afforded the tide compound as a colourless solid (0.74g) m.p.200- 202°C (from acetone-diethyl ether)
*H Nmr (CDC1 ) δ: 1.70 (2H, m), 1.93 (4H, m), 2.08 (IH, m), 2.26 (2H, m), 2.82 (IH, m), 3.37 (4H, m), 3.53 (IH, m), 4.18 (2H, m), 6.95 (7H, m), 7.30 (2H, m), 12.02 (IH, br.s). Example 33
(±) 4-[2-(4-Phenoxyphenoxy)ethyI]-l-azabicyclo[3.3.1]nonane hydrochloride (E33)
The title compound was prepared in a similar manner to Example 1 from (±) 4-(2- hydroxyethyl)-l-azabicyclo[3.3.1]nonane (O.llg, 0.65 mmol), 4-phenoxyphenol (0.18g, 0.98 mmol), triphenylphosphine (0.22g, 0.85 mmol) and diethyl azodicarboxylate (0.13 ml, 0.85 mmol). After stirring at room temperature for 2h the reaction was worked up as described in Example 1 to give the title compound as a colourless solid m.p. 195-197°C (methanol-diethyl ether).
!H Nmr (DMSO-d^) δ: 1.53-2.30 (10H, m), 3.05-3.60 (6H, m), 4.00 (2H, t, J=7Hz), 6.83-7.20 (7H, m), 7.35 (2H, t, J=7Hz).

Claims

Claims :
Use of a compound of formula (I):
Figure imgf000044_0001
Formula (I) in which
p, q and r each independently represent an integer from 1 to 4;
A is a bond, -CH=CH-, -C≡C-, oxygen, sulphur or NR*, where R is hydrogen, Cj.galkyl or phenylCχ_4alkyl;
n is 0 to 6, and m is 0 to 6, such that the length of the chain (CH2)nA(CH2)m is at least two atoms; and
Ar is aryl or heteroaryl, each of which may be optionally substituted;
or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment of disorders where a calcium channel antagonist is indicated.
2. Use of a compound according to claim 1 wherein the disorder is a condition or disease related to an accumulation of calcium in the brain cells of a mammal,
3. Use according to claim 1 or claim 2 wherein the disorder is anoxia, ischaemia, migraine, epilepsy, traumatic head injury, drug addiction withdrawal or AIDS- related dementia.
4. Use of a compound according to any of claims 1 to 3 wherein p and r are independently 2 or 3.
5. Use of a compound according to any of claims 1 to 4 wherein q is 1 or 2.
6. Use of a compound according to any of claims 1 to 5 wherein A is oxygen, -CH=CH- or a bond.
7. Use of a compound according to any of claims 1 to 6 wherein the length of the chain -(CH2)nA(CH2)m is from 2 to 6 atoms.
8. Use of a compound according to any of claims 1 to 7 wherein m is 0 to 3.
9. A compound of formula (IA) :
Figure imgf000045_0001
Formula (IA)
in which
p, q and r each independendy represent an integer from 1 to 4; n is 0 to 6; m is 0 to 6; and either
A is -C≡C- or NRl, where R is hydrogen, Cj.galkyl or phenylCχ_4alkyl; in which case Arl represents the group Ar as hereinbefore defined;
or A is a bond, in which case Ar* represents the group Ar as hereinbefore defined with the proviso that when each of p, q and r is 2 and Ar is phenyl substituted by one or two groups selected from halogen, Cχ_4alkoxy, nitro, cyano or amino, then the group -(CH2)nA(CH2) is not Cχ_4alkyl α to the quinuclidine nitrogen atom or C2-4alkyl β to the quinuclidine nitrogen atom,
or A is -CH=CH- in which case Ar* represents the group Ar as hereinbefore defined with the proviso that when each of p, q and r is 2; n and m are both zero and Ar is mono- or di-chlorophenyl, the group -(CH2)nA(CH2)m is not β to the quinuclidine nitrogen atom. or A is oxygen or sulphur in which case Ar* represents a group Ar2 which is phenyl substituted by a Cχ_2alkylenedioxy group or by 1 to 3 substituents selected from SCχ_4alkyl, OCF3, CF3s optionally substituted phenoxy, optionally substitoted phenylCι_4alkyl and optionally substituted phenylCχ_4alkoxy; or Ar2 is
an optionally substituted bicyclic or tricyclic aryl group of up to 15 carbon atoms;
an optionally substitued benzofuranyl group; or
an optionally substituted tricyclic heteroaryl group;
or a salt thereof.
10. A compound of formula (IB) :
Figure imgf000046_0001
Formula (IB)
wherein p, q, r, n, m and A are as defined for formula (IA) and R^ represents optionally substituted phenoxy, optionally substituted phenylCχ_4alkyl or optionally substitoted phenylCχ_4alkoxy, or R^ represents a fused benzene ring; or a salt thereof.
11. A compound of formual O
Figure imgf000046_0002
Formula (IC) wherein p, q, r, n, m and A are as defined for formula (IA) and Y and Z are as hereinbefore defined for formula 0); or a salt thereof.
12. A compound according to any of claims 9 to 11 wherein m is 0 to 3.
13. A compound of formula (I) selected from :
(±)3-(3,4-dichlorophenoxymethyl)- l-azabicyclo[2.2.2]octane;
(±)3-(4-benzyloxyphenoxymethyl)- 1 -azabicyclo[2.2.2]octane; (±)3-(4-benzylphenoxymethyl)- 1 -azabicyclo[2.2.2]octane;
(±)3-(2-phenylphenoxymethyl)-l-azabicyclo[2.2.2]octane;
(±)3-(4-tert-butylphenoxymethyl)- 1 -azabicyclo[2.2.2]octane;
(±)3-(l-naphthyloxymethyl)-l-azabicyclo[2.2.2]octane;
(±)3-(2-dibenzofuranyloxymethyl)-l-azabicyclo[2.2.2]octane; (±)3-(5-isoquinolinyloxy)methyl)-l-azabicyclo[2.2.2]octane;
(±) endo-3-(4-benzylphenoxymethyl)-l-azabicyclo[2.2. l]heptane;
(±) endo-3-(4-benzyloxyphenoxymethyl)- 1 -azabicyclo[2.2. l]heptane;
(±) exo-3-(4-benzylphenoxymethyl)-l-azabicyclo[2.2. l]heptane;
(±) exo-3-(4-benzyloxyphenoxymethyl)-l-azabicyclo[2.2. l]heptane; (±) E-3-[2-(l-naphthyl)ethenyl]-l-azabicyclo[2.2.2]octane;
(±)E-3-[2-(4-biphenyl)ethenyl]-l-azabicyclo[2.2.2]octane;
(±)3-[2-(l-naphthyl)ethyl]-l-azabicyclo[2.2.2]octane;
(±)3-[2-(4-biphenyl)ethyl]-l-azabicyclo[2.2.2]octane;
(±)E-3-[3-(l-naphtiιyl)prop-2-enyl]-l-azabicyclo[2.2.2]octane; (±)3-[3-(l-naphthyl)propyl]-l-azabicyclo[2.2.2]octane;
(±)3-[2-(2-dibenzofuranyloxy)ethyl]-l-azabicyclo[2.2.2]octane;
(±)3-[2-(4-benzyloxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane;
(±)3-[2-(4-benzylphenoxy)ethyl]-l-azabicyclo[2.2.2]octane;
(±)3-(4-phenoxyphenoxymethyl)-l-azabicyclo[2.2.2]octane; (+) 3-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane, (+) 3-[4-(2-dibenzofuranyloxy)butyl]- l-azabicyclo[2.2.2]octane, (+) 3-[4-(4-phenoxyphenoxy)butyl]-l-azabicyclo[2.2.2]octane, (±) 3-[3-(4-phenoxyphenoxy)propyl]- l-azabicyclo[2.2.2]octane, (+) 3-[2-[4-(2-phenylethyl)phenoxy]ethyl]-l-azabicyclo [2.2.2]octane, (±) 3-[2-[4-[2-(4-chlorophenyl)ethyl]phenoxy]ethyl]- l-azabicyclo[2.2.2]octane, Gfc) 3-[2-[5-(2-phenyl)benzo[b]furanyloxy]ethyl]-l-azabicyclo[2.2.2]octane, (+) 2-[2-(4-benzylphenoxy)ethyl]- l-azabicyclo[2.2.2]octane, (+) 2-[2-(4-benzyloxyphenoxy)ethyl]- l-azabicyclo[2.2.2]octane, (±) 2-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[2.2.2]octane, and (±) 4-[2-(4-phenoxyphenoxy)ethyl]-l-azabicyclo[3.3.1]nonane,
or a salt thereof.
14. A process for the preparation of a novel compound of formula 0) which comprises:
(a) for compounds of formula 0) in which A is O, S or NR*, reaction of a compound of formula (II):
Figure imgf000048_0001
Formula (II)
in which p, q, r and n are as described for formula 0) and A* is O, S or NR*, with a compound of formula L(CH2)mAr in which m and Ar are as described for formula 0). and L is a leaving group;
(b) for compounds of formula (I) in which A is O, S or NRl, reaction of a compound of formula (III):
Figure imgf000048_0002
Formula (IH) in which p, q, r and n are as described for formula (I) and L* is a group displaceable by a nucleophile, with a compound of formula HAl(CH2)mAr where m and Ar are as described for formula 0) and A * is as described for formula (II); or
(c) for compounds of formula (I) in which A is NR , reduction of a compotmd of formula (IV) :
Figure imgf000049_0001
Formula (IV)
in which R^ represents the group
-(CH2)nN(R1)C(O)(CH2)m.ι Ar or -(CH2)n.iC(O)N(Rl)(CH2)mAr,
and p, q, r, n, m, and Ar are as described for formula (I);
(d) for compounds of formula (I) in which A is a bond, reaction of a compound of formula (V) :
Figure imgf000049_0002
Formula (V)
(wherein L , p, q, r, m and n are as hereinbefore defined).
with a compound of formula X^Ar in which Ar is as described for formula (I), and X* is an alkali metal;
(e) For compounds wherein A is -CH=CH- reaction of a compound of formula (VI)
Figure imgf000050_0001
Formula (VD
(wherein n, p, q and r are as hereinbefore defined) with a Wittig reagent serving to introduce the group Ar;
(f) Interconversion of one compound of formula 0) to a different compound of formula 0) e.g. the reduction of a compound wherein A is -CH=CH- to a compound wherein A is -CH2CH2-;
and optionally thereafter forming a salt
15. A pharmaceutical composition comprising a novel compound of formula 0) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient.
16. A method of treatment of a condition or disease related to the accumulation of calcium in the brain cells of a mammal which comprises administering to a subject in need thereof an effective amount of a compound of formula 0) or a pharmaceutically acceptable salt thereof.
PCT/GB1993/000175 1992-01-28 1993-01-27 Azabricyclic compounds as calcium channel antagonists WO1993015073A1 (en)

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Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0600717A1 (en) * 1992-11-30 1994-06-08 Sankyo Company Limited Phenoxyalkylamines, -pyrrolidines and -piperidines for the treatment and prevention of circulatory diseases and psychosis
WO1994025459A1 (en) * 1993-04-29 1994-11-10 Zeneca Limited Heterocyclic derivatives
WO1995003302A1 (en) * 1993-07-20 1995-02-02 Smithkline Beecham Plc Quinolizidines with calcium channel antagonistic activity
WO1996026938A1 (en) * 1995-03-02 1996-09-06 Yamanouchi Pharmaceutical Co., Ltd. Novel quinuclidine derivatives having tricyclic fused hereto ring
US5554613A (en) * 1992-06-04 1996-09-10 Zeneca Limited Heterocyclic derivatives
US5612352A (en) * 1992-04-10 1997-03-18 Zeneca Limited Heterocyclic compounds
US5637596A (en) * 1994-05-24 1997-06-10 Pharmacia S.P.A. Azabicycloalkyl derivatives of imidazo[1,5-a]indol-3-one and process for their preparation
US5654315A (en) * 1991-12-23 1997-08-05 Imperial Chemical Industries Plc Quinuclidine compounds useful in treating diseases
US5691349A (en) * 1992-08-06 1997-11-25 Zeneca Limited Quinclidine derivatives as squalene synthase inhibitors
US5714496A (en) * 1992-08-28 1998-02-03 Zeneca Limited Quinuclidine derivatives as squalene synthase inhibitors
US5731323A (en) * 1992-12-21 1998-03-24 Zeneca Limited Quinuclidine derivatives as squalene synthase inhibitors
US5792777A (en) * 1991-10-30 1998-08-11 Zeneca Limited Biphenyl quinuclidines
WO1999015185A1 (en) * 1997-09-22 1999-04-01 Lisovenko, Vasily Trofimovich Agent for modifying the proliferation, functional activity and death of natural and tumoral cells
US6166052A (en) * 1998-03-11 2000-12-26 Warner-Lambert Company Heteroaryl alkyl alpha substituted peptidylamine calcium channel blockers
US6251919B1 (en) 1998-02-27 2001-06-26 Warner-Lambert Heterocyclic substituted aniline calcium channel blockers
WO2005016923A1 (en) * 2003-08-13 2005-02-24 Neurosearch A/S Novel quinuclidine derivatives and their pharmaceutical use
WO2005077899A3 (en) * 2004-02-04 2005-12-01 Abbott Lab Amino-substituted tricyclic derivatives and methods of use
US7094789B2 (en) 2002-07-22 2006-08-22 Asahi Kasei Pharma Corporation 5-substituted isoquinoline derivatives
US7365193B2 (en) 2004-02-04 2008-04-29 Abbott Laboratories Amino-substituted tricyclic derivatives and methods of use
US7417040B2 (en) 2004-03-01 2008-08-26 Bristol-Myers Squibb Company Fused tricyclic compounds as inhibitors of 17β-hydroxysteroid dehydrogenase 3
US7732477B2 (en) 2001-12-27 2010-06-08 Bayer Schering Pharma Aktiengesellschaft 2-heteroarylcarboxylic acid amides
US7795453B2 (en) 2002-07-29 2010-09-14 Bayer Schering Pharma Aktiengesellschaft Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US9108961B2 (en) 2010-05-17 2015-08-18 Forum Pharmaceuticals, Inc. Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride
US9585877B2 (en) 2012-05-08 2017-03-07 Forum Pharmaceuticals, Inc. Methods of maintaining, treating or improving cognitive function
JPWO2015182724A1 (en) * 2014-05-28 2017-04-20 トーアエイヨー株式会社 Substituted tropane derivatives
US9657010B2 (en) 2004-07-14 2017-05-23 Novartis Ag Substituted quinuclidines as alpha 7-nicotinic acetylcholine receptor activity modulators

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2323217C2 (en) * 2002-08-14 2008-04-27 Ньюросерч А/С Novel quinuclidine derivatives and their using

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0327155A2 (en) * 1988-01-30 1989-08-09 Merck Sharp & Dohme Ltd. Pyrazines, pyrimidines and pyridazines, useful in the treatment of senile dementia
EP0412797A2 (en) * 1989-08-08 1991-02-13 MERCK SHARP & DOHME LTD. The therapeutic use of substituted benzenes, formulations thereof and novel substituted benzenes
EP0416754A2 (en) * 1989-08-08 1991-03-13 MERCK SHARP & DOHME LTD. A novel substituted pyrazine, formulations thereof and use in medicine
WO1991014686A1 (en) * 1990-03-21 1991-10-03 Novo Nordisk A/S Azacyclic or azabicyclic compounds, their preparation and use
EP0470668A1 (en) * 1990-08-08 1992-02-12 MERCK SHARP & DOHME LTD. A process for preparing enantiomers of compounds having muscarinic activity
EP0473442A1 (en) * 1990-08-30 1992-03-04 MERCK SHARP & DOHME LTD. A substituted pyrazine and its salts, compositions containing them and their use in medicine
EP0492904A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted benzene derivatives for use in the treatment of glaucoma
EP0492902A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted pyridine derivatives for use in the treatment of glaucoma
EP0492903A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted pyrazines, pyrimidines and pyridazines for use in the treatment of glaucoma
EP0497415A1 (en) * 1991-02-01 1992-08-05 Akzo Nobel N.V. 3-Quinuclidine derivatives
WO1992015579A1 (en) * 1991-03-08 1992-09-17 Rhone-Poulenc Rorer International (Holdings) Inc. Multicyclic tertiary amine polyaromatic squalene synthetase inhibitors

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0327155A2 (en) * 1988-01-30 1989-08-09 Merck Sharp & Dohme Ltd. Pyrazines, pyrimidines and pyridazines, useful in the treatment of senile dementia
EP0412797A2 (en) * 1989-08-08 1991-02-13 MERCK SHARP & DOHME LTD. The therapeutic use of substituted benzenes, formulations thereof and novel substituted benzenes
EP0416754A2 (en) * 1989-08-08 1991-03-13 MERCK SHARP & DOHME LTD. A novel substituted pyrazine, formulations thereof and use in medicine
WO1991014686A1 (en) * 1990-03-21 1991-10-03 Novo Nordisk A/S Azacyclic or azabicyclic compounds, their preparation and use
EP0470668A1 (en) * 1990-08-08 1992-02-12 MERCK SHARP & DOHME LTD. A process for preparing enantiomers of compounds having muscarinic activity
EP0473442A1 (en) * 1990-08-30 1992-03-04 MERCK SHARP & DOHME LTD. A substituted pyrazine and its salts, compositions containing them and their use in medicine
EP0492904A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted benzene derivatives for use in the treatment of glaucoma
EP0492902A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted pyridine derivatives for use in the treatment of glaucoma
EP0492903A1 (en) * 1990-12-21 1992-07-01 MERCK SHARP & DOHME LTD. Substituted pyrazines, pyrimidines and pyridazines for use in the treatment of glaucoma
EP0497415A1 (en) * 1991-02-01 1992-08-05 Akzo Nobel N.V. 3-Quinuclidine derivatives
WO1992015579A1 (en) * 1991-03-08 1992-09-17 Rhone-Poulenc Rorer International (Holdings) Inc. Multicyclic tertiary amine polyaromatic squalene synthetase inhibitors

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 115, 1991, Columbus, Ohio, US; abstract no. 149760y, V.E. DEGTYAR ET AL. 'Common characteristics of calcium-channel and muscarinic-cholinergic receptor inhibitors.' page 18 ; *

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US5792777A (en) * 1991-10-30 1998-08-11 Zeneca Limited Biphenyl quinuclidines
US5770608A (en) * 1991-12-23 1998-06-23 Imperial Chemical Industries Plc Heterocyclic derivatives
US5654315A (en) * 1991-12-23 1997-08-05 Imperial Chemical Industries Plc Quinuclidine compounds useful in treating diseases
US5612352A (en) * 1992-04-10 1997-03-18 Zeneca Limited Heterocyclic compounds
US5554613A (en) * 1992-06-04 1996-09-10 Zeneca Limited Heterocyclic derivatives
US5691349A (en) * 1992-08-06 1997-11-25 Zeneca Limited Quinclidine derivatives as squalene synthase inhibitors
US5714496A (en) * 1992-08-28 1998-02-03 Zeneca Limited Quinuclidine derivatives as squalene synthase inhibitors
US5556864A (en) * 1992-11-30 1996-09-17 Sankyo Company, Limited α-ω-diarylalkane compounds serotonin-2 receptor agonists
EP0600717A1 (en) * 1992-11-30 1994-06-08 Sankyo Company Limited Phenoxyalkylamines, -pyrrolidines and -piperidines for the treatment and prevention of circulatory diseases and psychosis
US5731323A (en) * 1992-12-21 1998-03-24 Zeneca Limited Quinuclidine derivatives as squalene synthase inhibitors
WO1994025459A1 (en) * 1993-04-29 1994-11-10 Zeneca Limited Heterocyclic derivatives
US5919793A (en) * 1993-04-29 1999-07-06 Zeneca Limited Heterocyclic derivatives
WO1995003302A1 (en) * 1993-07-20 1995-02-02 Smithkline Beecham Plc Quinolizidines with calcium channel antagonistic activity
US5637596A (en) * 1994-05-24 1997-06-10 Pharmacia S.P.A. Azabicycloalkyl derivatives of imidazo[1,5-a]indol-3-one and process for their preparation
WO1996026938A1 (en) * 1995-03-02 1996-09-06 Yamanouchi Pharmaceutical Co., Ltd. Novel quinuclidine derivatives having tricyclic fused hereto ring
US5830902A (en) * 1995-03-02 1998-11-03 Yamanouchi Pharmaceutical Co., Ltd. Quinuclidine derivative having tricyclic hetero condensed ring
WO1999015185A1 (en) * 1997-09-22 1999-04-01 Lisovenko, Vasily Trofimovich Agent for modifying the proliferation, functional activity and death of natural and tumoral cells
US6251919B1 (en) 1998-02-27 2001-06-26 Warner-Lambert Heterocyclic substituted aniline calcium channel blockers
US6989448B2 (en) 1998-03-11 2006-01-24 Lain-Yen Hu Heteroaryl alkyl alpha substituted peptidylamine calcium channel blockers
US6469038B1 (en) 1998-03-11 2002-10-22 Warner-Lambert Company Heteroaryl alkyl alpha substituted peptidylamine calcium channel blockers
US6166052A (en) * 1998-03-11 2000-12-26 Warner-Lambert Company Heteroaryl alkyl alpha substituted peptidylamine calcium channel blockers
US8884017B2 (en) 2001-12-27 2014-11-11 Bayer Intellectual Property Gmbh 2-heteroarylcarboxylic acid amides
US8076355B2 (en) 2001-12-27 2011-12-13 Bayer Schering Pharma Aktiengesellschaft 2-heteroarylcarboxylic acid amides
US7732477B2 (en) 2001-12-27 2010-06-08 Bayer Schering Pharma Aktiengesellschaft 2-heteroarylcarboxylic acid amides
US7094789B2 (en) 2002-07-22 2006-08-22 Asahi Kasei Pharma Corporation 5-substituted isoquinoline derivatives
US9714242B2 (en) 2002-07-29 2017-07-25 Bayer Intellectual Property Gmbh Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US7795453B2 (en) 2002-07-29 2010-09-14 Bayer Schering Pharma Aktiengesellschaft Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US8153799B2 (en) 2002-07-29 2012-04-10 Bayer Schering Pharma Aktiengesellschaft Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US8772511B2 (en) 2002-07-29 2014-07-08 Bayer Intellectual Property Gmbh Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US10196388B2 (en) 2002-07-29 2019-02-05 Bayer Intellectual Property Gmbh Azabicyclic carbamates and their use as alpha-7 nicotinic acetylcholine receptor agonists
US7750022B2 (en) 2003-08-13 2010-07-06 Neurosearch A/S Quinuclidine derivatives and their pharmaceutical use
WO2005016923A1 (en) * 2003-08-13 2005-02-24 Neurosearch A/S Novel quinuclidine derivatives and their pharmaceutical use
US7365193B2 (en) 2004-02-04 2008-04-29 Abbott Laboratories Amino-substituted tricyclic derivatives and methods of use
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US7417040B2 (en) 2004-03-01 2008-08-26 Bristol-Myers Squibb Company Fused tricyclic compounds as inhibitors of 17β-hydroxysteroid dehydrogenase 3
US9657010B2 (en) 2004-07-14 2017-05-23 Novartis Ag Substituted quinuclidines as alpha 7-nicotinic acetylcholine receptor activity modulators
US9550767B2 (en) 2010-05-17 2017-01-24 Forum Pharmaceuticals, Inc. Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate
US9273044B2 (en) 2010-05-17 2016-03-01 Forum Pharmaceuticals, Inc. Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate
US9108961B2 (en) 2010-05-17 2015-08-18 Forum Pharmaceuticals, Inc. Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride
US9585877B2 (en) 2012-05-08 2017-03-07 Forum Pharmaceuticals, Inc. Methods of maintaining, treating or improving cognitive function
JPWO2015182724A1 (en) * 2014-05-28 2017-04-20 トーアエイヨー株式会社 Substituted tropane derivatives
US9856250B2 (en) 2014-05-28 2018-01-02 Toa Eiyo Ltd. Substituted tropane derivatives

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AU3364693A (en) 1993-09-01

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