JP2002527513A - ヒスタミン−ｈ３アゴニストまたはアンタゴニストとしてのｎ−（イミダゾリルアルキル）置換環式アミン - Google Patents

ヒスタミン−ｈ３アゴニストまたはアンタゴニストとしてのｎ−（イミダゾリルアルキル）置換環式アミン

Info

Publication number
JP2002527513A
JP2002527513A JP2000577165A JP2000577165A JP2002527513A JP 2002527513 A JP2002527513 A JP 2002527513A JP 2000577165 A JP2000577165 A JP 2000577165A JP 2000577165 A JP2000577165 A JP 2000577165A JP 2002527513 A JP2002527513 A JP 2002527513A
Authority
JP
Japan
Prior art keywords
compound
compound according
ring
aryl
substituted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2000577165A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002527513A5 (https=
Inventor
ロナルド ウォリン，
スチュアート ビー． ローゼンブラム，
アドリアーノ アフォンソ，
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Sharp and Dohme LLC
Original Assignee
Schering Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Schering Corp filed Critical Schering Corp
Publication of JP2002527513A publication Critical patent/JP2002527513A/ja
Publication of JP2002527513A5 publication Critical patent/JP2002527513A5/ja
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • 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
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics
    • 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
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • 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
    • A61P9/12—Antihypertensives
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Ophthalmology & Optometry (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2000577165A 1998-10-16 1999-10-15 ヒスタミン−ｈ３アゴニストまたはアンタゴニストとしてのｎ−（イミダゾリルアルキル）置換環式アミン Pending JP2002527513A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09/173,642 US6133291A (en) 1998-10-16 1998-10-16 N-(imidazolylalkyl)substituted cyclic amines as histamine-H3 agonists or antagonists
US09/173,642 1998-10-16
PCT/US1999/021461 WO2000023438A1 (en) 1998-10-16 1999-10-15 N-(imidazolylalkyl)substituted cyclic amines as histamine-h3 agonists or antagonists

Publications (2)

Publication Number Publication Date
JP2002527513A true JP2002527513A (ja) 2002-08-27
JP2002527513A5 JP2002527513A5 (https=) 2006-09-28

Family

ID=22632924

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000577165A Pending JP2002527513A (ja) 1998-10-16 1999-10-15 ヒスタミン−ｈ３アゴニストまたはアンタゴニストとしてのｎ−（イミダゾリルアルキル）置換環式アミン

Country Status (10)

Country Link
US (1) US6133291A (https=)
EP (1) EP1121354B1 (https=)
JP (1) JP2002527513A (https=)
CN (1) CN1198817C (https=)
AT (1) ATE284398T1 (https=)
AU (1) AU1092800A (https=)
CA (1) CA2346436A1 (https=)
DE (1) DE69922528T2 (https=)
ES (1) ES2229782T3 (https=)
WO (1) WO2000023438A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008543940A (ja) * 2005-06-20 2008-12-04 シェーリング コーポレイション ヒスタミンｈ３アンタゴニストとして有用な、炭素結合した置換ピペリジンおよびその誘導体

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7361666B2 (en) 1999-05-25 2008-04-22 Sepracor, Inc. Heterocyclic analgesic compounds and methods of use thereof
US6635661B2 (en) 2000-05-25 2003-10-21 Sepracor Inc. Heterocyclic analgesic compounds and methods of use thereof
US6677332B1 (en) 1999-05-25 2004-01-13 Sepracor, Inc. Heterocyclic analgesic compounds and methods of use thereof
US6645980B1 (en) 2000-05-25 2003-11-11 Sepracor Inc. Heterocyclic analgesic compounds and methods of use thereof
US6476050B2 (en) 2000-03-14 2002-11-05 Sepracor, Inc. 3-substituted piperidines comprising urea functionality, and methods of use thereof
ATE283853T1 (de) * 2000-09-20 2004-12-15 Schering Corp Substituierte imidazole als duale histamine h1 und h3 agonisten oder antagonisten
FR2827863A1 (fr) * 2001-07-27 2003-01-31 Sanofi Synthelabo Derives d'aminoalkylimidazole, leur preparation et leur utilisation en therapeutique
KR100432577B1 (ko) 2002-02-08 2004-05-24 주식회사유한양행 이미다졸 유도체의 제조방법
PT1499316E (pt) * 2002-04-18 2008-06-30 Schering Corp Derivados de (1-4-piperidinil)benzimidazole úteis como antagonistas de histamina h3
WO2004000831A1 (en) * 2002-06-24 2003-12-31 Schering Corporation Indole derivatives useful as histamine h3 antagonists
US7880017B2 (en) 2003-11-11 2011-02-01 Allergan, Inc. Process for the synthesis of imidazoles
US7183305B2 (en) 2003-11-11 2007-02-27 Allergan, Inc. Process for the synthesis of imidazoles
CL2007002958A1 (es) * 2006-10-12 2008-05-09 Epix Delaware Inc Compuestos derivados de heteroaril-carboxamida, antagonistas del receptor de quimioquina; composicion farmaceutica; y uso para el tratamiento o prevencion de enfermedades tales como rechazo de transplante de organos, artritis reumatoidea, lupus, entr
WO2009076512A1 (en) 2007-12-11 2009-06-18 Epix Delaware, Inc. Carboxamidξ compounds and their use as chemokine receptor agonists
WO2013151982A1 (en) 2012-04-03 2013-10-10 Arena Pharmaceuticals, Inc. Methods and compounds useful in treating pruritus, and methods for identifying such compounds
WO2016100940A1 (en) 2014-12-19 2016-06-23 The Broad Institute, Inc. Dopamine d2 receptor ligands
US10752588B2 (en) * 2014-12-19 2020-08-25 The Broad Institute, Inc. Dopamine D2 receptor ligands

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0358924A (ja) * 1989-07-25 1991-03-14 Smith Kline Ltd ヒスタミンｈ↓３―作動薬
JPH06511009A (ja) * 1991-12-18 1994-12-08 シェリング・コーポレーション 窒素含有４または５員複素環で置換されたイミダゾリルまたはイミダゾイルアルキル化合物
JPH06511252A (ja) * 1991-12-18 1994-12-15 シェリング・コーポレーション 窒素含有６員複素環で置換されたイミダゾイルアルキル化合物
JPH06511251A (ja) * 1991-12-18 1994-12-15 シェリング・コーポレーション ヒスタミンｈ↓３アゴニスト／アンタゴニストとしてのイミダゾリル−アルキル−ピペラジンおよび−ジアゼピン誘導体
WO1996040126A1 (en) * 1995-06-07 1996-12-19 Gliatech, Inc. 1h-4(5)-substituted imidazole derivatives
JPH10501001A (ja) * 1995-03-21 1998-01-27 アンスティテュ ナシオナル ドゥ ラ サントゥ エ ドゥ ラ ルシェルシュ メディカル（イーエヌエスエーエールエム） ヒスタミンｈ▲下３▼受容体−（アンタ）アゴニストイミダゾール誘導体類

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4006137A (en) * 1975-08-21 1977-02-01 E. R. Squibb & Sons, Inc. 2-Ethenyl imidazolium derivatives
ZA792608B (en) * 1978-05-30 1980-06-25 Smith Kline French Lab Nitro compounds
JPS6287573A (ja) * 1985-10-11 1987-04-22 Banyu Pharmaceut Co Ltd 四級アンモニウム塩の製造法
GB9115740D0 (en) * 1991-07-20 1991-09-04 Smithkline Beecham Plc Medicaments
US5807872A (en) * 1992-12-16 1998-09-15 Schering Corporation Imidazoylalkyl substituted with a six membered nitrogen containing heterocyclic ring
FI92843C (fi) * 1993-02-25 1995-01-10 Eija Anitta Maeensivu Uusi menetelmä optisesti aktiivisten glyserolijohdannaisten valmistamiseksi
ATE234290T1 (de) * 1993-11-15 2003-03-15 Schering Corp Phenylalkyl-imidazole als h3-rezeptor- antagonisten

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0358924A (ja) * 1989-07-25 1991-03-14 Smith Kline Ltd ヒスタミンｈ↓３―作動薬
JPH06511009A (ja) * 1991-12-18 1994-12-08 シェリング・コーポレーション 窒素含有４または５員複素環で置換されたイミダゾリルまたはイミダゾイルアルキル化合物
JPH06511252A (ja) * 1991-12-18 1994-12-15 シェリング・コーポレーション 窒素含有６員複素環で置換されたイミダゾイルアルキル化合物
JPH06511251A (ja) * 1991-12-18 1994-12-15 シェリング・コーポレーション ヒスタミンｈ↓３アゴニスト／アンタゴニストとしてのイミダゾリル−アルキル−ピペラジンおよび−ジアゼピン誘導体
JPH10501001A (ja) * 1995-03-21 1998-01-27 アンスティテュ ナシオナル ドゥ ラ サントゥ エ ドゥ ラ ルシェルシュ メディカル（イーエヌエスエーエールエム） ヒスタミンｈ▲下３▼受容体−（アンタ）アゴニストイミダゾール誘導体類
WO1996040126A1 (en) * 1995-06-07 1996-12-19 Gliatech, Inc. 1h-4(5)-substituted imidazole derivatives

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
JPN5001020822, Ｊ．−Ｃ．ＳＣＨＷＡＲＴＺ， Ｈ．Ｌ．ＨＡＡＳ（ＥＤＳ．）, ＴＨＥ ＨＩＳＴＡＭＩＮＥ ＲＥＣＥＰＴＥＲ, 1992, Ｐ５７−７２, US, ＷＩＬＥＹ−ＬＩＳＳ，ＩＮＣ． *
JPN6009060701, Ｊ．Ｍｅｄ．Ｃｈｅｍ．, 1996, ３９（５）, １１５７−１１６３ *
JPN6009060704, Ｊ．Ｍｅｄ．Ｃｈｅｍ．, 1996, ３９（１９）, ３８０６−３８１３ *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008543940A (ja) * 2005-06-20 2008-12-04 シェーリング コーポレイション ヒスタミンｈ３アンタゴニストとして有用な、炭素結合した置換ピペリジンおよびその誘導体

Also Published As

Publication number Publication date
ES2229782T3 (es) 2005-04-16
WO2000023438A1 (en) 2000-04-27
US6133291A (en) 2000-10-17
EP1121354A1 (en) 2001-08-08
EP1121354B1 (en) 2004-12-08
AU1092800A (en) 2000-05-08
CN1323302A (zh) 2001-11-21
CN1198817C (zh) 2005-04-27
CA2346436A1 (en) 2000-04-27
ATE284398T1 (de) 2004-12-15
DE69922528T2 (de) 2005-12-15
DE69922528D1 (de) 2005-01-13

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