WO2008010061A3 - 3-azabicyclo[3.1.0]hexanes ligands du récepteur vanilloïde, compositions pharmaceutiques les contenant et leurs procédés de préparation - Google Patents

3-azabicyclo[3.1.0]hexanes ligands du récepteur vanilloïde, compositions pharmaceutiques les contenant et leurs procédés de préparation Download PDF

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Publication number
WO2008010061A3
WO2008010061A3 PCT/IB2007/002002 IB2007002002W WO2008010061A3 WO 2008010061 A3 WO2008010061 A3 WO 2008010061A3 IB 2007002002 W IB2007002002 W IB 2007002002W WO 2008010061 A3 WO2008010061 A3 WO 2008010061A3
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Prior art keywords
azabicyclo
processes
hexane
receptor ligands
preparation
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PCT/IB2007/002002
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English (en)
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WO2008010061A2 (fr
Inventor
Laxmikant Atmaram Gharat
Neelima Khairatkar Joshi
Jitendra Maganbhai Gajera
Pravin Sabhajit Yadav
Original Assignee
Glenmark Pharmaceuticals Sa
Laxmikant Atmaram Gharat
Neelima Khairatkar Joshi
Jitendra Maganbhai Gajera
Pravin Sabhajit Yadav
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Application filed by Glenmark Pharmaceuticals Sa, Laxmikant Atmaram Gharat, Neelima Khairatkar Joshi, Jitendra Maganbhai Gajera, Pravin Sabhajit Yadav filed Critical Glenmark Pharmaceuticals Sa
Publication of WO2008010061A2 publication Critical patent/WO2008010061A2/fr
Publication of WO2008010061A3 publication Critical patent/WO2008010061A3/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/04—Antipruritics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/12—Keratolytics, e.g. wart or anti-corn preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/14—Drugs for dermatological disorders for baldness or alopecia
    • 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
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • A61P25/06—Antimigraine agents
    • 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
    • A61P25/22—Anxiolytics
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Dermatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La présente invention concerne des dérivés substitués de 3-azabicyclo[3.1.0]hexane utilisables en tant que ligands du récepteur vanilloïde, ainsi que des procédés qui les utilisent pour traiter des maladies, des affections et/ou des troubles induits par les récepteurs vanilloïdes et des procédés permettant de les préparer.
PCT/IB2007/002002 2006-07-17 2007-07-16 3-azabicyclo[3.1.0]hexanes ligands du récepteur vanilloïde, compositions pharmaceutiques les contenant et leurs procédés de préparation WO2008010061A2 (fr)

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
IN1136/MUM/2006 2006-07-17
IN1136MU2006 2006-07-17
US83556006P 2006-08-03 2006-08-03
US60/835,560 2006-08-03
IN381/MUM/2007 2007-02-27
IN381MU2007 2007-02-27
US89367507P 2007-03-08 2007-03-08
US60/893,675 2007-03-08
US94771507P 2007-07-03 2007-07-03
US60/947,715 2007-07-03

Publications (2)

Publication Number Publication Date
WO2008010061A2 WO2008010061A2 (fr) 2008-01-24
WO2008010061A3 true WO2008010061A3 (fr) 2008-04-17

Family

ID=38928004

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2007/002002 WO2008010061A2 (fr) 2006-07-17 2007-07-16 3-azabicyclo[3.1.0]hexanes ligands du récepteur vanilloïde, compositions pharmaceutiques les contenant et leurs procédés de préparation

Country Status (2)

Country Link
AR (1) AR061905A1 (fr)
WO (1) WO2008010061A2 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CL2008002053A1 (es) 2007-07-17 2009-05-22 Hoffmann La Roche Metodo para la purificacion de una eritropoyetina monopeguilada (epompeg) que consiste en proporcionar una solucion que contiene eritropoyetina mono, poli y no peguilada y hacerla pasar por dos pasos de cromatografia de intercambio cationico y metodo para producir epo mpeg que incluye metodo de purificacion.
AR067536A1 (es) 2007-07-17 2009-10-14 Hoffmann La Roche Metodo para obtener una eritropoyetina mono-pegilada en una forma sustancialmente homogenea
EP2025674A1 (fr) 2007-08-15 2009-02-18 sanofi-aventis Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament
WO2009034433A2 (fr) * 2007-09-10 2009-03-19 Glenmark Pharmaceuticals, S.A. Dérivés de 3-azabicyclo [3.1.0] hexane utilisés comme ligands des récepteurs vanilloïdes
WO2009090548A2 (fr) * 2008-01-17 2009-07-23 Glenmark Pharmaceuticals, S.A. Dérivés de 3-azabicyclo[3.1.0]hexane utilisés comme ligands des récepteurs vanilloïdes
CA2806634A1 (fr) * 2010-08-20 2012-02-23 Gruenenthal Gmbh Derives de carboxamide et d'uree cycliques substitues en tant que ligands du recepteur vanilloide
JP6774403B2 (ja) * 2014-06-12 2020-10-21 アロサイト ファーマスーティカルズ アーゲー 小分子ｌｆａ−１阻害薬
BR112021024108A2 (pt) 2019-05-31 2022-03-22 Ikena Oncology Inc Inibidores de tead e usos dos mesmos
MX2021014441A (es) 2019-05-31 2022-01-06 Ikena Oncology Inc Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos.
AU2020365108A1 (en) 2019-10-18 2022-04-21 Atengen, Inc. 3-phenylsulphonyl-quinoline derivatives as agents for treating pathogenic blood vessels disorders
RU2755206C1 (ru) 2020-05-20 2021-09-14 Федеральное государственное бюджетное учреждение науки Тихоокеанский институт биоорганической химии им. Г.Б. Елякова Дальневосточного отделения Российской академии наук (ТИБОХ ДВО РАН) Средство пролонгированного анальгетического действия и лекарственный препарат на его основе

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993018001A1 (fr) * 1992-03-02 1993-09-16 Pfizer Inc. Preparation d'intermediaires dans la synthese d'antibiotiques a la quinoline
US5475116A (en) * 1994-04-29 1995-12-12 Pfizer Inc. Aza bicyclo[3,1,0]hexane intermediates useful in the synthesis of quinolones
US6184380B1 (en) * 1999-01-25 2001-02-06 Pfizer Inc. Process for preparing naphthyridones and intermediates
US6194438B1 (en) * 1998-12-02 2001-02-27 Pfizer Inc. Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one, and compositions and methods for inhibiting abnormal cell growth comprising said derivatives
WO2002090326A1 (fr) * 2001-05-02 2002-11-14 Smithkline Beecham P.L.C. Urees heterocycliques, leur preparation et leur utilisation comme antagonistes du recepteur vanilloide
WO2004052857A1 (fr) * 2002-12-10 2004-06-24 Ranbaxy Laboratories Limited Derives d'azabicyclo [3.1.0] hexane 3,6-disubstitues utilises comme antagonistes du recepteur muscarinique
WO2004078749A1 (fr) * 2003-03-06 2004-09-16 Glaxo Group Limited Derives d'uree heterocycliques pour le traitement de la douleur
WO2005051390A1 (fr) * 2003-10-29 2005-06-09 Merck Sharp & Dohme Limited Derives de 4-fluoro-4-(pyridin-2-yl)-piperidine-1-carboxamide et composes associes modulant la fonction du recepteur vanilloide (vr1) pour le traitement de la douleur
WO2007029086A2 (fr) * 2005-09-05 2007-03-15 Ranbaxy Laboratories Limited Derives de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-iv
WO2007077508A2 (fr) * 2005-12-30 2007-07-12 Ranbaxy Laboratories Limited Dérivés de bêta-aminoacides comme inhibiteurs de la dipeptidylpeptidase iv

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993018001A1 (fr) * 1992-03-02 1993-09-16 Pfizer Inc. Preparation d'intermediaires dans la synthese d'antibiotiques a la quinoline
US5475116A (en) * 1994-04-29 1995-12-12 Pfizer Inc. Aza bicyclo[3,1,0]hexane intermediates useful in the synthesis of quinolones
US6194438B1 (en) * 1998-12-02 2001-02-27 Pfizer Inc. Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one, and compositions and methods for inhibiting abnormal cell growth comprising said derivatives
US6184380B1 (en) * 1999-01-25 2001-02-06 Pfizer Inc. Process for preparing naphthyridones and intermediates
WO2002090326A1 (fr) * 2001-05-02 2002-11-14 Smithkline Beecham P.L.C. Urees heterocycliques, leur preparation et leur utilisation comme antagonistes du recepteur vanilloide
WO2004052857A1 (fr) * 2002-12-10 2004-06-24 Ranbaxy Laboratories Limited Derives d'azabicyclo [3.1.0] hexane 3,6-disubstitues utilises comme antagonistes du recepteur muscarinique
WO2004078749A1 (fr) * 2003-03-06 2004-09-16 Glaxo Group Limited Derives d'uree heterocycliques pour le traitement de la douleur
WO2005051390A1 (fr) * 2003-10-29 2005-06-09 Merck Sharp & Dohme Limited Derives de 4-fluoro-4-(pyridin-2-yl)-piperidine-1-carboxamide et composes associes modulant la fonction du recepteur vanilloide (vr1) pour le traitement de la douleur
WO2007029086A2 (fr) * 2005-09-05 2007-03-15 Ranbaxy Laboratories Limited Derives de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-iv
WO2007077508A2 (fr) * 2005-12-30 2007-07-12 Ranbaxy Laboratories Limited Dérivés de bêta-aminoacides comme inhibiteurs de la dipeptidylpeptidase iv

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CHEM. EUROP. J., vol. 8, no. 16, 2002, pages 3789 - 3801 *
DATABASE BEILSTEIN BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002465472, Database accession no. BRN:8563110 *
DATABASE BEILSTEIN BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002465473, Database accession no. BRN:9222926 *
ELMAR VILSMAIER ET AL: "Reductive decyanation of N-protected 6-Amino-3-azabicyclo(3.1.0)hexan ecarbonitriles", TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol. 54, no. 23, 1998, pages 6403 - 6414, XP002081309, ISSN: 0040-4020 *
GILLASPY M L ET AL: "A Simple Method for the Formation of Cyclopropylamines: The First Synthesis of Tricyclopropylamine", TETRAHEDRON LETTERS, ELSEVIER, AMSTERDAM, NL, vol. 36, no. 41, 9 October 1995 (1995-10-09), pages 7399 - 7402, XP004027008, ISSN: 0040-4039 *
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AR061905A1 (es) 2008-10-01
WO2008010061A2 (fr) 2008-01-24

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