WO2007034282A3 - Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a - Google Patents

Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a Download PDF

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Publication number
WO2007034282A3
WO2007034282A3 PCT/IB2006/002568 IB2006002568W WO2007034282A3 WO 2007034282 A3 WO2007034282 A3 WO 2007034282A3 IB 2006002568 W IB2006002568 W IB 2006002568W WO 2007034282 A3 WO2007034282 A3 WO 2007034282A3
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WIPO (PCT)
Prior art keywords
diaryl
heterocycle
receptor antagonists
imidazole compounds
compounds condensed
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PCT/IB2006/002568
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English (en)
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WO2007034282A2 (fr
Inventor
Michelle Marie Claffey
Steven Wayne Goldstein
Stanley Jung
Arthur Nagel
Volker Shulze
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Pfizer Prod Inc
Michelle Marie Claffey
Steven Wayne Goldstein
Stanley Jung
Arthur Nagel
Volker Shulze
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Application filed by Pfizer Prod Inc, Michelle Marie Claffey, Steven Wayne Goldstein, Stanley Jung, Arthur Nagel, Volker Shulze filed Critical Pfizer Prod Inc
Publication of WO2007034282A2 publication Critical patent/WO2007034282A2/fr
Publication of WO2007034282A3 publication Critical patent/WO2007034282A3/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention porte sur des composés aryles substitués imidazo[4,5-c] pyridine. Ces composés sont utiles dans des compositions pharmaceutiques comme antagonistes du C3a pour traiter différents états médicaux associés à la cascade du complément. L'invention porte également sur des méthodes de traitement desdits états.
PCT/IB2006/002568 2005-09-19 2006-09-18 Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a WO2007034282A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71851705P 2005-09-19 2005-09-19
US60/718,517 2005-09-19

Publications (2)

Publication Number Publication Date
WO2007034282A2 WO2007034282A2 (fr) 2007-03-29
WO2007034282A3 true WO2007034282A3 (fr) 2007-05-18

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Family Applications (1)

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PCT/IB2006/002568 WO2007034282A2 (fr) 2005-09-19 2006-09-18 Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a

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US11566026B2 (en) 2016-12-22 2023-01-31 Incyte Corporation Heterocyclic compounds as immunomodulators

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JP4101852B2 (ja) 2004-05-26 2008-06-18 エーザイ・アール・アンド・ディー・マネジメント株式会社 シンナミド化合物
CA2580119A1 (fr) 2004-10-26 2006-05-04 Eisai R & D Management Co., Ltd. Forme amorphe d'un derive de cinnamide
KR20080069221A (ko) 2005-11-24 2008-07-25 에자이 알앤드디 매니지먼트 가부시키가이샤 모르폴린 타입의 신나미드 화합물
TWI370130B (en) 2005-11-24 2012-08-11 Eisai R&D Man Co Ltd Two cyclic cinnamide compound
TWI378091B (en) 2006-03-09 2012-12-01 Eisai R&D Man Co Ltd Multi-cyclic cinnamide derivatives
US7737141B2 (en) 2006-07-28 2010-06-15 Eisai R&D Management Co., Ltd. Prodrug of cinnamide compound
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US7935815B2 (en) 2007-08-31 2011-05-03 Eisai R&D Management Co., Ltd. Imidazoyl pyridine compounds and salts thereof
TW200916469A (en) * 2007-08-31 2009-04-16 Eisai R & Amp D Man Co Ltd Multi-cyclic compounds
JP5669579B2 (ja) 2007-09-05 2015-02-12 ザ ガバナーズ オブ ザ ユニバーシティ オブ アルバータ オルト置換アリールボロン酸を使用する化学反応のためのカルボン酸の有機触媒活性化方法
CA2704137A1 (fr) * 2007-10-30 2009-05-07 Nihon Medi-Physics Co., Ltd. Utilisation d'un nouveau compose presentant une affinite pour les substances amyloides et procede de production dudit compose
US8445674B2 (en) 2009-10-21 2013-05-21 Hoffmann-La Roche Inc Heterocyclyl compounds
PL2547678T3 (pl) * 2010-03-18 2016-10-31 Związki przeciwzapalne
US8410117B2 (en) * 2010-03-26 2013-04-02 Hoffmann-La Roche Inc. Imidazopyrimidine derivatives
CA2820262A1 (fr) 2010-12-08 2012-06-14 Vanderbilt University Utilisation de composes bicycliques de pyrazole en tant que modulateurs allosteriques des recepteurs mglur5
WO2012125732A1 (fr) * 2011-03-15 2012-09-20 Vanderbilt University Imadazapyrinidin-5(6h)-ones substituées en tant que modulateurs allostériques des récepteurs mglur5
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BR112015025140A2 (pt) * 2013-05-23 2017-07-18 Hoffmann La Roche 2-fenilimidazo[1,2-a]pirimidinas como agentes de imagem
AU2016269839B2 (en) 2015-06-03 2021-07-08 The University Of Queensland Mobilizing agents and uses therefor
MA52119A (fr) 2015-10-19 2018-08-29 Ncyte Corp Composés hétérocycliques utilisés comme immunomodulateurs
SG11201804152RA (en) 2015-11-19 2018-06-28 Incyte Corp Heterocyclic compounds as immunomodulators
CN105439965B (zh) * 2015-11-20 2018-05-22 江苏恒安化工有限公司 喹喔啉杂环及其衍生物的合成方法
ES2844374T3 (es) 2015-12-22 2021-07-22 Incyte Corp Compuestos heterocíclicos como inmunomoduladores
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CN106588673B (zh) * 2016-12-20 2018-06-26 金凯(辽宁)化工有限公司 一种2-甲基-5-氨基三氟甲苯的制备方法
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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2343748A1 (fr) * 1976-03-10 1977-10-07 Metabio Derives de 2,3-dihydro imidazo (2,1-b) thiazole, leur procede de preparation et leur application en therapeutique
EP0404190A1 (fr) * 1989-06-23 1990-12-27 Takeda Chemical Industries, Ltd. Composés hétérocycliques condensés, leur préparation et leur utilisation
WO1999015490A1 (fr) * 1997-09-23 1999-04-01 Smithkline Beecham Corporation Ligands pour recepteurs de c3a
JPH11116481A (ja) * 1997-10-06 1999-04-27 Sumitomo Pharmaceut Co Ltd スタット6活性化阻害剤
WO2001057038A1 (fr) * 2000-02-01 2001-08-09 Basf Aktiengesellschaft Composes heterocycliques et leur utilisation comme inhibiteurs de parp
US6551723B1 (en) * 1998-08-18 2003-04-22 Fuji Photo Film Co., Ltd. Organic electroluminescence element material and organic electroluminescence element comprising same
JP2003277743A (ja) * 2002-03-22 2003-10-02 Idemitsu Kosan Co Ltd 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子
WO2004063159A1 (fr) * 2003-01-10 2004-07-29 Idemitsu Kosan Co., Ltd. Derive heterocyclique azote et element electroluminescent organique utilisant ce derive
WO2005043630A1 (fr) * 2003-10-31 2005-05-12 Idemitsu Kosan Co., Ltd. Transistor a couches minces organique

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2343748A1 (fr) * 1976-03-10 1977-10-07 Metabio Derives de 2,3-dihydro imidazo (2,1-b) thiazole, leur procede de preparation et leur application en therapeutique
EP0404190A1 (fr) * 1989-06-23 1990-12-27 Takeda Chemical Industries, Ltd. Composés hétérocycliques condensés, leur préparation et leur utilisation
WO1999015490A1 (fr) * 1997-09-23 1999-04-01 Smithkline Beecham Corporation Ligands pour recepteurs de c3a
JPH11116481A (ja) * 1997-10-06 1999-04-27 Sumitomo Pharmaceut Co Ltd スタット6活性化阻害剤
US6551723B1 (en) * 1998-08-18 2003-04-22 Fuji Photo Film Co., Ltd. Organic electroluminescence element material and organic electroluminescence element comprising same
WO2001057038A1 (fr) * 2000-02-01 2001-08-09 Basf Aktiengesellschaft Composes heterocycliques et leur utilisation comme inhibiteurs de parp
JP2003277743A (ja) * 2002-03-22 2003-10-02 Idemitsu Kosan Co Ltd 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子
WO2004063159A1 (fr) * 2003-01-10 2004-07-29 Idemitsu Kosan Co., Ltd. Derive heterocyclique azote et element electroluminescent organique utilisant ce derive
EP1582516A1 (fr) * 2003-01-10 2005-10-05 Idemitsu Kosan Co., Ltd. Derive heterocyclique azote et element electroluminescent organique utilisant ce derive
WO2005043630A1 (fr) * 2003-10-31 2005-05-12 Idemitsu Kosan Co., Ltd. Transistor a couches minces organique
EP1679747A1 (fr) * 2003-10-31 2006-07-12 Idemitsu Kosan Co., Ltd. Transistor a couches minces organique

Non-Patent Citations (13)

* Cited by examiner, † Cited by third party
Title
A. ANDREANI, M.RAMBALDI, A. LOCATELLI, AM. ISETTA: "synthesis and mitogenic activity of new imidazo[2,1-b]thiazoles", EUR. J. MED., vol. 26, 1991, pages 335 - 337, XP009080499 *
B. MEKONNEN, G. CRANK, D. CRAIG: "a new and facile synthesis of imidazo[2,1-b]oxazoles", J. HETEROCYCLIC CHEM., vol. 34, 1997, pages 589 - 599, XP002424348 *
BARLIN G B ET AL: "IMIDAZO1,2-BPYRIDAZINES. XXI. SYNTHESES OF SOME 3-ACYLAMINOMETHYL-6-(CHLORO AND IODO)-2-(SUBSTITUTED PHENYL) IMIDAZO1,2-BPYRIDAZINES AND -IMIDAZO 1,2-APYRIDINES AND THEIR INTERACTION WITH CENTRAL AND MITOCHONDRIAL BENZODIAZEPINE RECEPTORS", AUSTRALIAN JOURNAL OF CHEMISTRY, vol. 50, 1997, pages 61 - 67, XP001007026, ISSN: 0004-9425 *
BUU-HOI, NG. PH. ET AL: "Biphenyl analogs of p-hydroxypropiophenone", RECUEIL DES TRAVAUX CHIMIQUES DES PAYS-BAS ET DE LA BELGIQUE , 72, 774-80 CODEN: RTCPB4; ISSN: 0370-7539, 1953, XP002016690 *
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; XP002424408, Database accession no. beilstein RN : 1022905 *
F. BARBA, B. BATANERO: "a novel and convenient electrochemical synthesis of 3,7-diaryl-2H-imidazo[2,1-b][1,3,4]oxadiazines", JOURNAL OF ORGANIC CHEMISTRY, vol. 58, no. 24, 1993, pages 6889 - 6891, XP009080473 *
FANG, CHONGBO ET AL: "Synthesis and luteal cell killing activity of 2-substituted phenyl-1,2,4- triazolo [5,1-a]pyridine derivatives", ZHONGGUO YAOWU HUAXUE ZAZHI , 12(3), 134-137, 163 CODEN: ZYHZEF; ISSN: 1005-0108, 2002, XP009080425 *
G. B. BARLIN, L.P. DAVIES, S.J. IRELAND, J. ZHANG: "Imidazo1,2-b]pyridazines. part XIII", AUST. J. CHEM., vol. 45, 1992, pages 1281 - 1300, XP009080477 *
GRANT E B ET AL: "Design, synthesis, and biological activity of diiminoisoindolines as complement component 3a antagonists", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, OXFORD, GB, vol. 11, no. 21, 2001, pages 2817 - 2820, XP002984323, ISSN: 0960-894X *
ISMAIL, MOHAMED A. ET AL: "Novel Dicationic Imidazo[1,2-a]pyridines and 5,6,7,8-Tetrahydro- imidazo[1,2-a]pyridines as Antiprotozoal Agents", JOURNAL OF MEDICINAL CHEMISTRY , 47(14), 3658-3664 CODEN: JMCMAR; ISSN: 0022-2623, 2004, XP002424347 *
LIU, TAO ET AL: "Non-steroidal pregnancy-terminating agents: design, synthesis and structure-activity relationships of 2-aryl-1,2,4- triazolo [1,5-a]pyridine", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS , 12(17), 2411-2413 CODEN: BMCLE8; ISSN: 0960-894X, 2002, XP002424346 *
PAUCHARD, JEAN PAUL ET AL: "Anil synthesis. 17. Preparation of styryl derivatives of 2-phenyl-4H-1,2,4- triazolo [1,5-a]pyridine", HELVETICA CHIMICA ACTA , 61(1), 142-70 CODEN: HCACAV; ISSN: 0018-019X, 1978, XP002424345 *
S.N. SAWHNEY, D.R. KODALI, G.S. DHINDSA, S.P. SINGH: "synthesis & antiinflammatory activity of some arylimidazo[2,1-b]thiazolyl- & arylimidazo[2,1-b]benzothiazolyl-acetic acids", INDIAN JOURNAL OF CHEMISTRY, vol. 21b, February 1982 (1982-02-01), pages 134 - 138, XP009080136 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11566026B2 (en) 2016-12-22 2023-01-31 Incyte Corporation Heterocyclic compounds as immunomodulators

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