PE20060604A1 - Derivados del tetrahidronaftaleno como agentes antiinflamatorios y procedimiento para su preparacion - Google Patents
Derivados del tetrahidronaftaleno como agentes antiinflamatorios y procedimiento para su preparacionInfo
- Publication number
- PE20060604A1 PE20060604A1 PE2004001100A PE2004001100A PE20060604A1 PE 20060604 A1 PE20060604 A1 PE 20060604A1 PE 2004001100 A PE2004001100 A PE 2004001100A PE 2004001100 A PE2004001100 A PE 2004001100A PE 20060604 A1 PE20060604 A1 PE 20060604A1
- Authority
- PE
- Peru
- Prior art keywords
- tetrahydronaphthalen
- dihydroxy
- trifluoromethyl
- fluoro
- hydroxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 229940121363 anti-inflammatory agent Drugs 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical class F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical class [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 108090001007 Interleukin-8 Proteins 0.000 abstract 1
- 206010006451 bronchitis Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 210000001616 monocyte Anatomy 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 230000028327 secretion Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/58—Naphthylamines; N-substituted derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Quinoline Compounds (AREA)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA (I) DONDE R1 Y R2 SON H, HALOGENO, PERFLUORALQUILO(C1-C5), ENTRE OTROS; R11 ES H, HALOGENO, CIANO, ENTRE OTROS; R12 ES H, HIDROXI, CIANO, ENTRE OTROS; R3 ES ALQUILO(C1-C10) OPCIONALMENTE SUSTITUIDO, CICLOALQUILO(C3-C7), HETEROCICLILO, ENTRE OTROS; R4 ES HIDROXI, OR10, O(CO)R10 DONDE R10 ES HIDROXI, ALQUILO(C1-C10); R5 ES ALQUILO(C1-C10), CICLOALQUILO(C3-C7), ALQUELINO(C2-C8), ENTRE OTROS; R6 Y R7 SON H, METILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-{[8-FLUORO-2,5-DIHIDROXI-4,4-DIMETIL-2-(TRIFLUOROMETIL)-1,2,3,4-TETRAHIDRONAFTALEN-1-IL]AMINO}-2,3-DIHIDROISOINDOL-1-ONA, 5-{[7-CLORO-2,5-DIHIDROXI-4,4-DIMETIL-2-(TRIFLUOROMETIL)-1,2,3,4-TETRAHIDRONAFTALEN-1-IL]AMINO}-ISOQUINOLIN-1(2H)-ONA, 4-{[8-FLUORO-2,5-DIHIDROXI-4,4-DIMETIL-2-(TRIFLUOROMETIL)-1,2,3,4-TETRAHIDRONAFTALEN-1-IL]AMINO}-6-FLUORO-2,3-DIHIDROISOINDOL-1-ONA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION. ESTOS COMPUESTOS INHIBEN LA SECRECION PRODUCIDA POR LIPOPOLISACARIDO (LPS) DE LA CITOQUINA IL-8 EN MONOCITOS. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES TALES COMO BRONQUITIS, ARTRITIS REUMATOIDE
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10347386A DE10347386B4 (de) | 2003-10-08 | 2003-10-08 | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
DE10347383A DE10347383A1 (de) | 2003-10-08 | 2003-10-08 | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
DE102004017662A DE102004017662B3 (de) | 2004-04-05 | 2004-04-05 | Mehrfach substituierte Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20060604A1 true PE20060604A1 (es) | 2006-08-04 |
Family
ID=34437487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2004001100A PE20060604A1 (es) | 2003-10-08 | 2004-11-11 | Derivados del tetrahidronaftaleno como agentes antiinflamatorios y procedimiento para su preparacion |
Country Status (29)
Country | Link |
---|---|
US (1) | US7659297B2 (es) |
EP (1) | EP1670458B1 (es) |
JP (1) | JP4638438B2 (es) |
AR (1) | AR046062A1 (es) |
AT (1) | ATE348609T1 (es) |
AU (1) | AU2004280088B2 (es) |
BR (1) | BRPI0415209A (es) |
CA (1) | CA2539587A1 (es) |
CR (1) | CR8357A (es) |
CY (1) | CY1107596T1 (es) |
DE (1) | DE502004002403D1 (es) |
DK (1) | DK1670458T3 (es) |
EA (1) | EA010186B1 (es) |
EC (1) | ECSP066539A (es) |
ES (1) | ES2279454T3 (es) |
HK (1) | HK1097734A1 (es) |
HN (1) | HN2004000446A (es) |
IL (1) | IL174405A (es) |
ME (1) | MEP15908A (es) |
MY (1) | MY141853A (es) |
NO (1) | NO20062020L (es) |
NZ (1) | NZ546473A (es) |
PE (1) | PE20060604A1 (es) |
PL (1) | PL1670458T3 (es) |
PT (1) | PT1670458E (es) |
RS (1) | RS20060250A (es) |
SI (1) | SI1670458T1 (es) |
TW (1) | TWI306455B (es) |
WO (1) | WO2005034939A1 (es) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7638515B2 (en) | 2003-10-08 | 2009-12-29 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7662821B2 (en) | 2003-10-08 | 2010-02-16 | Bayer Schering Pharma Ag | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
RS20060250A (en) | 2003-10-08 | 2008-08-07 | Schering Aktiengesellschaft, | 1-amino-2-oxy-substituted tetrahydronaphtalene derivatives, method for the production thereof, and their use as antiphlogistics |
US20080153859A1 (en) | 2004-04-05 | 2008-06-26 | Hartmut Rehwinkel | Multiply-substituted tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
DE102004044680B3 (de) * | 2004-09-09 | 2006-06-08 | Schering Ag | Alkyliden-Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer sowie diese enthaltende pharmazeutische Präparate |
US20060084652A1 (en) * | 2004-09-09 | 2006-04-20 | Stefan Baeurle | Alkylidene-tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US20060167025A1 (en) * | 2004-12-22 | 2006-07-27 | Markus Berger | Tricyclic amino alcohols, processes for synthesis of same and use of same as anti-inflammatory drugs |
DE102004063227A1 (de) * | 2004-12-22 | 2006-07-06 | Schering Ag | Tricylische Aminoalkohole, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
US20060247292A1 (en) * | 2005-03-22 | 2006-11-02 | Hartmut Rehwinkel | Benzocycloheptene derivatives, process for their production and their use as anti-inflammatory agents |
US20060229305A1 (en) * | 2005-03-22 | 2006-10-12 | Markus Berger | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7297700B2 (en) | 2005-03-24 | 2007-11-20 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
DE102005017286B3 (de) * | 2005-04-14 | 2006-12-28 | Schering Ag | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
EP1834948A1 (de) | 2006-03-15 | 2007-09-19 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
TWI464148B (zh) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為p2x7調節劑之雙環雜芳基化合物與其用途 |
EA200801997A1 (ru) | 2006-04-20 | 2009-04-28 | Глаксо Груп Лимитед | Новые соединения |
EP1917963A1 (en) * | 2006-10-31 | 2008-05-07 | Bayer Schering Pharma Aktiengesellschaft | Cyclic phenyl-substituted indazols, a process for their production and their use as anti-inflammatory agents |
EP1958934A1 (en) * | 2007-02-16 | 2008-08-20 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalenylamides, a process for their production and their use as anti-inflammatory agents |
EP2072509A1 (en) | 2007-12-18 | 2009-06-24 | Bayer Schering Pharma Aktiengesellschaft | 1-Aryl-1H-quinoline-2-ones: process for their production and their use as anti-inflammatory agents |
US8236786B2 (en) | 2008-08-07 | 2012-08-07 | Pulmagen Therapeutics (Inflammation) Limited | Respiratory disease treatment |
EA019441B1 (ru) | 2008-12-30 | 2014-03-31 | Палмаджен Терепьютикс (Инфлеммейшн) Лимитед | Сульфонамиды, предназначенные для лечения респираторных нарушений |
WO2010150014A1 (en) | 2009-06-24 | 2010-12-29 | Pulmagen Therapeutics (Inflammation) Limited | 5r- 5 -deuterated glitazones for respiratory disease treatment |
SG178174A1 (en) | 2009-07-31 | 2012-03-29 | Cadila Healthcare Ltd | Novel compounds as modulators of glucocorticoid receptors |
WO2011098746A1 (en) | 2010-02-09 | 2011-08-18 | Pulmagen Therapeutics (Inflammation) Limited | Crystalline acid addition salts of ( 5r) -enanti0mer of pioglitazone |
GB201002224D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
GB201002243D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
WO2019016110A1 (en) * | 2017-07-18 | 2019-01-24 | Lonza Ltd | PROCESS FOR THE PREPARATION OF 5-FLUORO-2-METHYL-3-NITROBENZOIC ACID AND METHYL ESTER |
US11001552B2 (en) | 2017-07-18 | 2021-05-11 | Lonza Ltd | Method for preparation of 5-fluoro-2-methyl-3-nitrobenzoic acid and its methyl ester |
PL233977B1 (pl) * | 2018-01-10 | 2019-12-31 | Politechnika Warszawska | Sposób otrzymywania 7-metoksy-1,2,3-tris(4-metoksyfenylo)- 1,2,3,4-tetrahydronaftalenu |
Family Cites Families (59)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE791474A (fr) | 1971-11-25 | 1973-03-16 | Yamanouchi Pharma Co Ltd | Procede de preparation de derives d'acides cycloalcoylaminoarylcarboxyliques |
US4720537A (en) | 1985-11-25 | 1988-01-19 | E. I. Du Pont De Nemours And Company | Branched copolyetherketones |
JPS63220242A (ja) | 1987-03-10 | 1988-09-13 | Fuji Photo Film Co Ltd | フオトレジスト組成物 |
JPH02501737A (ja) | 1987-05-15 | 1990-06-14 | シェリング・コーポレーション | アリール置換ナフタリン,ベンゾオキセピン,ベンズアゼピン,ベンゾシクロヘプテン誘導体 |
US5225436A (en) | 1987-05-15 | 1993-07-06 | Schering Corporation | Aryl substituted naphthalene derivatives |
EP0370056A1 (de) | 1987-07-16 | 1990-05-30 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Neue diazole |
US5059609A (en) | 1987-10-19 | 1991-10-22 | Pfizer Inc. | Substituted tetralins, chromans and related compounds in the treatment of asthma, arthritis and related diseases |
JPH0717589B2 (ja) * | 1990-01-22 | 1995-03-01 | ファイザー製薬株式会社 | 新規1,3―ジカルボニル化合物およびその組成物 |
JPH0641038A (ja) | 1992-07-17 | 1994-02-15 | Mitsubishi Kasei Corp | カルボン酸誘導体 |
JP2002504066A (ja) | 1994-12-29 | 2002-02-05 | アラーガン、セイルズ、インコーポレイテッド | 5または8置換テトラヒドロナフチルまたはジヒドロナフチル基と、アリールまたはヘテロアリール基とでジ置換された、レチノイド様生物学的活性を有するアセチレン |
US5489584A (en) * | 1994-12-29 | 1996-02-06 | Allergan, Inc. | Acetylenes disubstituted with a 5-amino or substituted 5-amino substituted tetrahydronaphthyl group and with an aryl or heteroaryl group having retinoid-like biological activity |
CU23088A3 (es) | 1997-03-24 | 2005-10-19 | Altana Pharma Ag | Compuestos de tetra-hidropiridina. |
EP1003495A4 (en) | 1997-07-22 | 2002-08-28 | Lilly Co Eli | PHARMACEUTICAL COMPOUNDS |
GB9716244D0 (en) | 1997-07-31 | 1997-10-08 | Electrophoretics International | Pharmaceutical compounds |
US6333337B1 (en) | 1998-01-27 | 2001-12-25 | Icagen, Inc. | Potassium channel inhibitors |
US7468422B2 (en) * | 1998-03-05 | 2008-12-23 | Centre National De La Recherche Scientifique - Cnrs | Mechanosensitive mammalian potassium channel activatable by polyunsaturated fatty acids |
US6013830A (en) | 1998-03-30 | 2000-01-11 | Sepracor Inc. | Asymmetric grignard synthesis with cyclic 1,2 aminoalcohols |
AU5682299A (en) | 1998-08-21 | 2000-03-14 | Scripps Research Institute, The | Catalytic asymmetric aminohydroxylation with amino-substituted heterocycles |
JP2000256255A (ja) | 1999-03-10 | 2000-09-19 | Kuraray Co Ltd | (±)−トランス−ペルメトリン酸の光学分割法 |
SE9903930D0 (sv) | 1999-10-29 | 1999-10-29 | Astra Pharma Inc | Novel compounds and a novel process for their preparation |
DE10038639A1 (de) | 2000-07-28 | 2002-02-21 | Schering Ag | Nichtsteroidale Entzündungshemmer |
ATE393141T1 (de) * | 2000-08-21 | 2008-05-15 | Pacific Corp | Neue thiourea-derivate und pharmazeutische zusammensetzungen die diese enthalten |
ES2193839B1 (es) | 2001-06-22 | 2005-02-16 | Almirall Prodesfarma, S.A. | Nuevos derivados de 6-fenildihidropirrolpirimidindiona. |
CA2461218C (en) | 2001-09-21 | 2011-02-01 | Eli Lilly And Company | Muscarinic agonists |
GT200200188A (es) | 2001-09-24 | 2003-06-25 | Preparacion y uso de derivados de imidazol para el tratamiento de la obesidad | |
DK1446387T3 (da) * | 2001-11-21 | 2009-12-21 | Pharmacia & Upjohn Co Llc | Substituerede aryl, 1,4-pyrazinderivater |
US6875866B2 (en) | 2002-02-21 | 2005-04-05 | Schering Corporation | Process for synthesis of D1 receptor antagonists |
ES2298508T3 (es) | 2002-03-26 | 2008-05-16 | Boehringer Ingelheim Pharmaceuticals Inc. | Mimeticos de glucocorticoides, metodos para prepararlos, composiciones farmaceuticas y sus usos. |
US6897224B2 (en) | 2002-04-02 | 2005-05-24 | Schering Ag | Quinoline and isoquinoline derivatives, a process for their production and their use as inflammation inhibitors |
DE10215316C1 (de) | 2002-04-02 | 2003-12-18 | Schering Ag | Chinolin- und Isochinolin-Derivate, ein pharmazeutisches Mittel und ihre Verwendung als Entzündungshemmer |
JP4722490B2 (ja) | 2002-08-26 | 2011-07-13 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | シクロペンタ[b]ナフタレン誘導体 |
CA2512257A1 (en) | 2003-01-03 | 2004-07-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1-propanol and 1-propylamine derivatives and their use as glucocorticoid ligands |
US20040224992A1 (en) | 2003-02-27 | 2004-11-11 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
US20050090559A1 (en) | 2003-07-01 | 2005-04-28 | Markus Berger | Heterocyclically-substituted pentanol derivatives, process for their production and their use as anti-inflammatory agents |
MXPA06000169A (es) | 2003-07-01 | 2006-04-27 | Schering Ag | Derivados de pentanol heterociclicamente sustituidos, procedimiento para su preparacion y su uso como anti-inflamatorios. |
WO2005021682A1 (de) | 2003-08-22 | 2005-03-10 | Merck Patent Gmbh | Cyclopenta[a]naphthalinderivate |
CN1239441C (zh) | 2003-09-12 | 2006-02-01 | 中国科学院上海有机化学研究所 | 利用固载化的双辛可尼类生物碱配体催化不对称羟胺化和双羟化反应的方法 |
RS20060250A (en) | 2003-10-08 | 2008-08-07 | Schering Aktiengesellschaft, | 1-amino-2-oxy-substituted tetrahydronaphtalene derivatives, method for the production thereof, and their use as antiphlogistics |
US7662821B2 (en) * | 2003-10-08 | 2010-02-16 | Bayer Schering Pharma Ag | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7638515B2 (en) * | 2003-10-08 | 2009-12-29 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7179919B2 (en) | 2004-03-18 | 2007-02-20 | Boehringer Ingelheim Pharmaceuticals, Inc. | Stereoselective synthesis of certain trifluoromethyl-substituted alcohols |
US20080153859A1 (en) | 2004-04-05 | 2008-06-26 | Hartmut Rehwinkel | Multiply-substituted tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US20050222154A1 (en) * | 2004-04-05 | 2005-10-06 | Hartmut Rehwinkel | Multiply-substituted tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
GB0418045D0 (en) | 2004-08-12 | 2004-09-15 | Glaxo Group Ltd | Compounds |
DE102004044680B3 (de) | 2004-09-09 | 2006-06-08 | Schering Ag | Alkyliden-Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer sowie diese enthaltende pharmazeutische Präparate |
US20060084652A1 (en) | 2004-09-09 | 2006-04-20 | Stefan Baeurle | Alkylidene-tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US20060165615A1 (en) * | 2004-11-23 | 2006-07-27 | Shende Rajesh V | Non-oxidative tooth whiteners for dentifrice application |
US20060167025A1 (en) | 2004-12-22 | 2006-07-27 | Markus Berger | Tricyclic amino alcohols, processes for synthesis of same and use of same as anti-inflammatory drugs |
DE102004063227A1 (de) | 2004-12-22 | 2006-07-06 | Schering Ag | Tricylische Aminoalkohole, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
US20060229305A1 (en) | 2005-03-22 | 2006-10-12 | Markus Berger | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
DE102005014089A1 (de) | 2005-03-22 | 2006-09-28 | Schering Ag | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
US20060247292A1 (en) | 2005-03-22 | 2006-11-02 | Hartmut Rehwinkel | Benzocycloheptene derivatives, process for their production and their use as anti-inflammatory agents |
US20070015750A1 (en) | 2005-04-14 | 2007-01-18 | Stefan Baeurle | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US20070015761A1 (en) | 2005-04-14 | 2007-01-18 | Anne Mengel | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
ES2414479T3 (es) | 2005-04-14 | 2013-07-19 | Glaxo Group Limited | Indazoles como ligandos del receptor de glucocorticoides |
US20070129359A1 (en) | 2005-04-14 | 2007-06-07 | Christoph Huwe | Tetrahydronaphthalene derivatives, processes for their preparation and their use as antiinflammatory agents |
DE102005017286B3 (de) | 2005-04-14 | 2006-12-28 | Schering Ag | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
JP4980366B2 (ja) | 2005-12-09 | 2012-07-18 | エフ.ホフマン−ラ ロシュ アーゲー | 抗炎症剤としてのグルココルチコイド受容体モジュレーター |
EP1834948A1 (de) | 2006-03-15 | 2007-09-19 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
-
2004
- 2004-10-06 RS YUP-2006/0250A patent/RS20060250A/sr unknown
- 2004-10-06 EP EP04790271A patent/EP1670458B1/de not_active Expired - Lifetime
- 2004-10-06 NZ NZ546473A patent/NZ546473A/en not_active IP Right Cessation
- 2004-10-06 PT PT04790271T patent/PT1670458E/pt unknown
- 2004-10-06 CA CA002539587A patent/CA2539587A1/en not_active Abandoned
- 2004-10-06 ME MEP-159/08A patent/MEP15908A/xx unknown
- 2004-10-06 SI SI200430231T patent/SI1670458T1/sl unknown
- 2004-10-06 PL PL04790271T patent/PL1670458T3/pl unknown
- 2004-10-06 AT AT04790271T patent/ATE348609T1/de active
- 2004-10-06 JP JP2006530142A patent/JP4638438B2/ja not_active Expired - Fee Related
- 2004-10-06 DE DE502004002403T patent/DE502004002403D1/de not_active Expired - Lifetime
- 2004-10-06 ES ES04790271T patent/ES2279454T3/es not_active Expired - Lifetime
- 2004-10-06 WO PCT/EP2004/011370 patent/WO2005034939A1/de active IP Right Grant
- 2004-10-06 BR BRPI0415209-3A patent/BRPI0415209A/pt not_active IP Right Cessation
- 2004-10-06 AU AU2004280088A patent/AU2004280088B2/en not_active Ceased
- 2004-10-06 EA EA200600621A patent/EA010186B1/ru not_active IP Right Cessation
- 2004-10-06 DK DK04790271T patent/DK1670458T3/da active
- 2004-10-08 MY MYPI20044145A patent/MY141853A/en unknown
- 2004-10-08 AR ARP040103651A patent/AR046062A1/es not_active Application Discontinuation
- 2004-10-08 TW TW093130577A patent/TWI306455B/zh not_active IP Right Cessation
- 2004-10-08 US US10/960,754 patent/US7659297B2/en not_active Expired - Fee Related
- 2004-11-03 HN HN2004000446A patent/HN2004000446A/es unknown
- 2004-11-11 PE PE2004001100A patent/PE20060604A1/es not_active Application Discontinuation
-
2006
- 2006-03-20 IL IL174405A patent/IL174405A/en not_active IP Right Cessation
- 2006-04-24 CR CR8357A patent/CR8357A/es not_active Application Discontinuation
- 2006-05-02 EC EC2006006539A patent/ECSP066539A/es unknown
- 2006-05-05 NO NO20062020A patent/NO20062020L/no not_active Application Discontinuation
-
2007
- 2007-02-15 HK HK07101854.6A patent/HK1097734A1/xx not_active IP Right Cessation
- 2007-03-20 CY CY20071100384T patent/CY1107596T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20060604A1 (es) | Derivados del tetrahidronaftaleno como agentes antiinflamatorios y procedimiento para su preparacion | |
PE20060185A1 (es) | ANTAGONISTA DEL RECEPTOR A2A DE LA ADENOSINA CON ESTRUCTURA DE PIRAZOLO--[4,3-e]-1,2,4-TRIAZOLO-[1,5-c]-PIRIMIDINA | |
PE20020366A1 (es) | Derivados de piperazina como ligandos del receptor 5ht2 | |
PE20060010A1 (es) | 2,3,4,5-TETRAHIDRO-1H-BENZO[d]AZEPINAS 6-SUSTITUIDAS COMO AGONISTAS DEL RECEPTOR 5-HT2C | |
PE20070808A1 (es) | COMPUESTOS DERIVADOS DE ISOQUINOLINA COMO INHIBIDORES DE Rho-QUINASA | |
PE20120058A1 (es) | Derivados de imidazopirazina como inhibidores de syk | |
PE20051141A1 (es) | Inhibidores de la polimerasa viral | |
PE20090960A1 (es) | Derivados de quinazolinadiona, su preparacion y sus aplicaciones terapeuticas | |
PE20030039A1 (es) | Derivados de indol con afinidad por el receptor 5-ht6 | |
PE20080842A1 (es) | Benzoxazoles y oxazolopiridinas que son utiles como inhibidores de las cinasas janus | |
PE20061106A1 (es) | Derivados de 2-(4-oxo-4h-quinazolin-3-il)acetamida | |
PE20050194A1 (es) | Derivados de piridina-2-carboxamida como activadores de glucoquinasa | |
PE20080211A1 (es) | Compuestos derivados de 6-(bencilo sustituido con heterociclilo)-4-oxoquinolina como inhibidores de integrasa del vih | |
PE20080841A1 (es) | Derivados de quinazolinona e isoquinolinona y su uso para el tratamiento o prevencion de trastornos relacionados con el estres o la depresion | |
PE20060957A1 (es) | Compuestos pirazolopiridinas su preparacion y composiciones farmaceuticas | |
PE20141827A1 (es) | Inhibidores de proteinas quinasas | |
PE20090441A1 (es) | DERIVADOS DE IMIDAZO[1,2-a]PIRIDIN-2-ILMETIL PIPERIDINA SUSTITUIDA | |
CO5721002A2 (es) | Derivados de acido 3-(4-benciloxifenil) propanoico | |
PE20040914A1 (es) | Derivados de pirrolopirimidina como inhibidores de tirosina quinasas | |
PE20070407A1 (es) | Compuestos derivados de pirazina como antagonistas del receptor a2b de adenosina | |
PE20030940A1 (es) | Derivados de piridina y pirimidina | |
EA200801001A1 (ru) | Соединения, которые обладают активностью по отношению к рецепторам м, и их применения в медицине | |
PE20120593A1 (es) | Derivados fusionados de pirimidin-4-ona como antagonistas del receptor de angiotensina ii y como agonistas del receptor ppar gamma | |
PE20021043A1 (es) | DERIVADOS DE PIRAZINO[1,2-a]INDOL COMO AGONISTAS DEL RECEPTOR 5HT2 | |
PE20011030A1 (es) | Combinaciones farmaceuticas que comprenden tegaserod y omeprazol |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |