JP2003509494A - ムスカリン拮抗薬 - Google Patents

ムスカリン拮抗薬

Info

Publication number
JP2003509494A
JP2003509494A JP2001524970A JP2001524970A JP2003509494A JP 2003509494 A JP2003509494 A JP 2003509494A JP 2001524970 A JP2001524970 A JP 2001524970A JP 2001524970 A JP2001524970 A JP 2001524970A JP 2003509494 A JP2003509494 A JP 2003509494A
Authority
JP
Japan
Prior art keywords
compound
formula
added
etoac
compounds
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
JP2001524970A
Other languages
English (en)
Japanese (ja)
Other versions
JP2003509494A5 (enExample
Inventor
ジョン ダブリュー. クレイダー,
ジョセフ エイ. コズロウスキ,
スチュアート ダブリュー. マッコンビー,
マイケル ダブリュー. ミラー,
スーザン エフ. ヴァイス,
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 JP2003509494A publication Critical patent/JP2003509494A/ja
Publication of JP2003509494A5 publication Critical patent/JP2003509494A5/ja
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/30Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
    • C07D211/32Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
JP2001524970A 1999-09-22 2000-07-05 ムスカリン拮抗薬 Pending JP2003509494A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US40139199A 1999-09-22 1999-09-22
US09/401,391 1999-09-22
PCT/US2000/018358 WO2001021590A1 (en) 1999-09-22 2000-07-05 Muscarinic antagonists

Publications (2)

Publication Number Publication Date
JP2003509494A true JP2003509494A (ja) 2003-03-11
JP2003509494A5 JP2003509494A5 (enExample) 2007-08-16

Family

ID=23587566

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001524970A Pending JP2003509494A (ja) 1999-09-22 2000-07-05 ムスカリン拮抗薬

Country Status (14)

Country Link
EP (1) EP1214299B1 (enExample)
JP (1) JP2003509494A (enExample)
CN (1) CN1167682C (enExample)
AR (1) AR025459A1 (enExample)
AT (1) ATE264301T1 (enExample)
AU (1) AU5786300A (enExample)
CA (1) CA2384018C (enExample)
CO (1) CO5180624A1 (enExample)
DE (1) DE60009931T2 (enExample)
ES (1) ES2215055T3 (enExample)
HK (1) HK1043590A1 (enExample)
MX (1) MXPA02003136A (enExample)
PE (1) PE20010649A1 (enExample)
WO (1) WO2001021590A1 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL117149A0 (en) * 1995-02-23 1996-06-18 Schering Corp Muscarinic antagonists
CN1301972C (zh) * 2001-10-10 2007-02-28 先灵公司 作为毒覃碱拮抗剂的哌啶化合物
JPWO2004069828A1 (ja) * 2003-02-04 2006-05-25 三菱ウェルファーマ株式会社 ピペリジン化合物およびその医薬用途
EP2533645B1 (en) 2010-02-09 2016-07-27 The Johns Hopkins University Methods and compositions for improving cognitive function
WO2014078568A1 (en) 2012-11-14 2014-05-22 The Johns Hopkins University Methods and compositions for treating schizophrenia
JP6478923B2 (ja) 2013-02-07 2019-03-06 ヘプタレス セラピューティクス リミテッドHeptares Therapeutics Limited ムスカリンm4受容体アゴニストとしてのピペリジン−1−イル及びアゼピン−1−イルカルボキシレート
CN105142623A (zh) 2013-03-15 2015-12-09 艾吉因生物股份有限公司 用于改善认知功能的方法和组合物
EP2968237A4 (en) 2013-03-15 2016-08-31 Univ Johns Hopkins METHOD AND COMPOSITIONS FOR IMPROVING COGNITIVE FUNCTION
CN107810002B (zh) 2015-05-22 2021-01-05 艾吉因生物股份有限公司 左乙拉西坦的延时释放药物组合物
HK1253029A1 (zh) 2015-11-06 2019-06-06 Neurocrine Biosciences, Inc. 作为毒蕈碱性受体4(m4)拮抗剂用於治疗神经系统疾病的n-[2-(1-苄基哌啶-4-基)乙基]-4-(吡嗪-2-基)-哌嗪-1-甲酰胺衍生物及相关化合物
EP4069367B1 (en) 2019-12-06 2024-05-15 Neurocrine Biosciences, Inc. Muscarinic receptor 4 antagonists and methods of use

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11501014A (ja) * 1995-02-23 1999-01-26 シェーリング コーポレイション ムスカリン様アンタゴニストとしてのベンジルピペリジンおよびピペラジン
JP2000501117A (ja) * 1996-08-08 2000-02-02 シェーリング コーポレイション ムスカリン様アンタゴニスト
JP2002519349A (ja) * 1998-06-30 2002-07-02 シェーリング コーポレイション ムスカリン性アンタゴニスト

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5691323A (en) * 1995-05-12 1997-11-25 Merck & Co., Inc. Muscarine antagonists
US6066636A (en) * 1998-06-30 2000-05-23 Schering Corporation Muscarinic antagonists

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11501014A (ja) * 1995-02-23 1999-01-26 シェーリング コーポレイション ムスカリン様アンタゴニストとしてのベンジルピペリジンおよびピペラジン
JP2000501117A (ja) * 1996-08-08 2000-02-02 シェーリング コーポレイション ムスカリン様アンタゴニスト
JP2002519349A (ja) * 1998-06-30 2002-07-02 シェーリング コーポレイション ムスカリン性アンタゴニスト

Also Published As

Publication number Publication date
CA2384018A1 (en) 2001-03-29
HK1043590A1 (zh) 2002-09-20
AR025459A1 (es) 2002-11-27
ES2215055T3 (es) 2004-10-01
AU5786300A (en) 2001-04-24
EP1214299B1 (en) 2004-04-14
DE60009931T2 (de) 2005-04-07
DE60009931D1 (de) 2004-05-19
CN1374949A (zh) 2002-10-16
CA2384018C (en) 2010-01-12
ATE264301T1 (de) 2004-04-15
CN1167682C (zh) 2004-09-22
PE20010649A1 (es) 2001-06-19
WO2001021590A1 (en) 2001-03-29
CO5180624A1 (es) 2002-07-30
EP1214299A1 (en) 2002-06-19
MXPA02003136A (es) 2002-09-30

Similar Documents

Publication Publication Date Title
US6294554B1 (en) Muscarinic antagonists
AU701452B2 (en) Benzylpiperidines and piperazines as muscarinic antagonists
JP4012068B2 (ja) ムスカリンアンタゴニスト
CA2263167C (en) Ether muscarinic antagonists
AU2003262420A1 (en) Derivatives of N-[phenyl(piperidin-2-yl)methyl]benzamide, the preparation method thereof and application of same in therapeutics
CA2259655C (en) 1,4-di-sustituted piperidines as muscarinic antagonists
EP0100200A1 (en) 2-Substituted 4-amino-6,7-dimethoxyquinolines
NO781935L (no) Fremgangsmaate ved fremstilling av fthalazinderivater
EP0937715B1 (en) Tetrahydrobenzindole compounds
JP3269574B2 (ja) メタノアントラセン化合物、これを含有する神経精神障害を治療するための調剤学的組成物、およびこの化合物を製造するための方法および中間体
JP2003509494A (ja) ムスカリン拮抗薬
US4243666A (en) 4-Amino-2-piperidino-quinazolines
EP0326106B1 (en) Alkylene diamines
EP1630159A1 (en) 5-HT7 receptor antagonists
US5472966A (en) Antidepressant heteroarylaminoalkyl derivatives of naphthyl-monazines
SK137597A3 (en) 1-£'omega'-(3,4-dihydro-2-naphthalenyl)alkyl| cyclic amine derivatives, process for producing the same, and medicinal composition containing the same
WO2007139211A1 (ja) 光学活性ピペリジン化合物の製法
JPH0741481A (ja) 両性型三環系化合物
EP0707579B1 (en) Piperidinyl substituted methanoanthracenes as d1/d2-antagonists and 5ht2-serotanin-antagonists
JPWO2000053600A1 (ja) 新規ピペリジン誘導体
CS214797B2 (cs) Způsob výroby nových derivátů 4-amino-2-piperidinochinazolinu
IE47977B1 (en) 6,7-di(loweralkoxy)-4-amino-2-(substituted piperidino)quinazolines
WO2012085935A2 (en) Compounds as inhibitors of renin

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20070620

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20070620

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A132

Effective date: 20100706

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20101005

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20101013

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20101105

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20101112

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20110624