FI113178B - Menetelmä valmistaa terapeuttisesti arvokas 5,6-dihydro-4H-tiatsolo[5,4-d]-, -oksatsolo[4,5-d]- tai - imidatso[4,5-d][1]-bentsatsepiini-6-fenyylikarbonyylijohdannainen - Google Patents

Menetelmä valmistaa terapeuttisesti arvokas 5,6-dihydro-4H-tiatsolo[5,4-d]-, -oksatsolo[4,5-d]- tai - imidatso[4,5-d][1]-bentsatsepiini-6-fenyylikarbonyylijohdannainen Download PDF

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Publication number
FI113178B
FI113178B FI960260A FI960260A FI113178B FI 113178 B FI113178 B FI 113178B FI 960260 A FI960260 A FI 960260A FI 960260 A FI960260 A FI 960260A FI 113178 B FI113178 B FI 113178B
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FI
Finland
Prior art keywords
group
carbonyl
benzazepin
benzazepine
formula
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Application number
FI960260A
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English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI960260A0 (fi
FI960260A (fi
Inventor
Akira Matsuhisa
Nobuaki Taniguchi
Akihiro Tanaka
Ken-Ichiro Sakamoto
Hiroyuki Koshio
Takeyuki Yatsu
Atsuki Yamazaki
Original Assignee
Yamanouchi Pharma Co Ltd
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Application filed by Yamanouchi Pharma Co Ltd filed Critical Yamanouchi Pharma Co Ltd
Publication of FI960260A0 publication Critical patent/FI960260A0/fi
Publication of FI960260A publication Critical patent/FI960260A/fi
Application granted granted Critical
Publication of FI113178B publication Critical patent/FI113178B/fi

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    • 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
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • 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
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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
    • A61P9/08—Vasodilators for multiple indications
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16—Benzazepines; Hydrogenated benzazepines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic 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
    • C07D513/02—Heterocyclic 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
    • C07D513/04—Ortho-condensed systems

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Output Control And Ontrol Of Special Type Engine (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
FI960260A 1993-07-21 1996-01-19 Menetelmä valmistaa terapeuttisesti arvokas 5,6-dihydro-4H-tiatsolo[5,4-d]-, -oksatsolo[4,5-d]- tai - imidatso[4,5-d][1]-bentsatsepiini-6-fenyylikarbonyylijohdannainen FI113178B (fi)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP18043593 1993-07-21
JP18043593 1993-07-21
PCT/JP1994/001183 WO1995003305A1 (fr) 1993-07-21 1994-07-19 Derive de benzazepine de fusion et composition pharmaceutique renfermant ce derive
JP9401183 1994-07-19

Publications (3)

Publication Number Publication Date
FI960260A0 FI960260A0 (fi) 1996-01-19
FI960260A FI960260A (fi) 1996-01-19
FI113178B true FI113178B (fi) 2004-03-15

Family

ID=16083198

Family Applications (1)

Application Number Title Priority Date Filing Date
FI960260A FI113178B (fi) 1993-07-21 1996-01-19 Menetelmä valmistaa terapeuttisesti arvokas 5,6-dihydro-4H-tiatsolo[5,4-d]-, -oksatsolo[4,5-d]- tai - imidatso[4,5-d][1]-bentsatsepiini-6-fenyylikarbonyylijohdannainen

Country Status (18)

Country Link
US (2) US5723606A (fr)
EP (2) EP0709386B1 (fr)
KR (1) KR100304331B1 (fr)
CN (1) CN1040210C (fr)
AT (2) ATE277003T1 (fr)
AU (2) AU683483B2 (fr)
CA (1) CA2167673C (fr)
DE (2) DE69434032T2 (fr)
ES (2) ES2228405T3 (fr)
FI (1) FI113178B (fr)
HU (1) HUT74582A (fr)
NO (1) NO306303B1 (fr)
NZ (1) NZ268671A (fr)
PL (1) PL177738B1 (fr)
RU (1) RU2129123C1 (fr)
TW (1) TW279163B (fr)
UA (1) UA64690C2 (fr)
WO (1) WO1995003305A1 (fr)

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US5693635A (en) * 1993-07-29 1997-12-02 American Cyanamid Company Tricyclic benzazepine vasopressin antagonists
AR002459A1 (es) * 1995-01-17 1998-03-25 American Cyanamid Co Antagonistas de vasopresina de benzacepina triciclicos, una composicion farmaceutica que los contiene, un metodo para tratar enfermedades y unprocedimiento para su preparacion.
US6268359B1 (en) 1998-01-28 2001-07-31 Senju Pharmaceutical Co., Ltd. Preventives or remedies for vision disorders
AR018818A1 (es) * 1998-04-03 2001-12-12 Yamano Masaki Una composicion farmaceutica para la terapia de un edema.
AU4168999A (en) * 1998-06-19 2000-01-05 Wakamoto Pharmaceutical Co., Ltd. Ocular tension lowering agents and phosphoric ester derivatives
US7015212B1 (en) 1999-05-12 2006-03-21 The United States Of America As Represented By The Department Of Health And Human Services Thiazepine inhibitors of HIV-1 integrase
US6765004B1 (en) * 1999-06-17 2004-07-20 Ortho-Mcneil Pharmaceutical, Inc. Indoloazepines as vasopressin receptor antagonists
US6437006B1 (en) 1999-09-27 2002-08-20 American Cyanamid Company Pharmaceutical carrier formulation
WO2001054698A1 (fr) * 2000-01-26 2001-08-02 Warner-Lambert Company Procede permettant d'empecher ou de traiter des occlusions intestinales postoperatoires
ES2272341T3 (es) * 2000-01-26 2007-05-01 Astellas Pharma Inc. Combinaciones de inhibidores de enzima y de antagonistas.
US20030103983A1 (en) * 2002-05-09 2003-06-05 Pressler Milton Lethan Ace inhibitor-vasopressin antagonist combinations
US20030008860A1 (en) * 2002-05-09 2003-01-09 Bakker-Arkema Rebecca Guggemos Treatment of congestive heart failure
AU779929B2 (en) * 2000-10-04 2005-02-17 Warner-Lambert Company Treatment of pulmonary hypertension
ES2288899T3 (es) 2000-10-04 2008-02-01 Astellas Pharma Inc. Uso de un antagonista de vasopresina tal como conivaptan en la fabricacion de un medicamento para el tratamiento de la hipertension pulmonar.
AU2002224115A1 (en) * 2000-11-28 2002-06-11 Yamanouchi Pharmaceutical Co., Ltd. 1,4,5,6-tetrahydroimidazo(4,5-d)diazepine derivatives or salts thereof
CN103214450B (zh) * 2005-12-28 2016-10-05 弗特克斯药品有限公司 作为atp-结合盒转运蛋白调节剂的1-(苯并[d][1,3]间二氧杂环戊烯-5-基)-n-(苯基)环丙烷-甲酰胺衍生物
US7671221B2 (en) * 2005-12-28 2010-03-02 Vertex Pharmaceuticals Incorporated Modulators of ATP-Binding Cassette transporters
US20080221084A1 (en) * 2006-10-30 2008-09-11 Otsuka Pharmaceutical Co., Ltd. Method for reducing infarction using vasopressin antagonist compounds, and compositions and combinations therefor
US20090069295A1 (en) * 2007-09-09 2009-03-12 Protia, Llc Deuterium-enriched conivaptan
JP2011509261A (ja) * 2008-01-07 2011-03-24 シンタ ファーマシューティカルズ コーポレーション 炎症および免疫関連用途向けの化合物
US8263630B2 (en) * 2008-02-12 2012-09-11 Bristol-Myers Squibb Company 1,2,3-triazoles as 11-beta hydroxysteroid dehydrogenase type I inhibitors
CA2728767A1 (fr) * 2008-06-26 2009-12-30 Amgen Inc. Alcools d'alcynyle utilises comme inhibiteurs de kinases
CN102753530B (zh) 2009-10-26 2015-06-17 大塚制药株式会社 苯并氮杂*化合物
WO2014062888A1 (fr) 2012-10-18 2014-04-24 University Of South Florida Compositions et procédés de traitement d'accident vasculaire cérébral
CN103497195B (zh) * 2013-10-21 2016-01-27 北京科莱博医药开发有限责任公司 盐酸考尼伐坦新晶型及其制备方法
CN105310978A (zh) * 2014-08-04 2016-02-10 李峰 一种含有活性成分盐酸考尼伐坦的药物组合物及其制剂
CN105884778A (zh) * 2014-09-24 2016-08-24 李峰 一种化合物和制备方法
CN105153168A (zh) * 2015-09-29 2015-12-16 上海天慈国际药业有限公司 N-[4-(2-甲基-4,5-二氢-3H-咪唑并[4,5-d][1]苯并氮杂卓-6-甲酰基)苯基]-2-苯基苯甲酰胺盐酸盐的制备方法
CN106317060B (zh) * 2016-08-22 2019-02-15 山东罗欣药业集团恒欣药业有限公司 一种盐酸考尼伐坦的制备方法
US11498903B2 (en) 2017-08-17 2022-11-15 Bristol-Myers Squibb Company 2-(1,1′-biphenyl)-1H-benzodimidazole derivatives and related compounds as apelin and APJ agonists for treating cardiovascular diseases
HU231206B1 (hu) 2017-12-15 2021-10-28 Richter Gedeon Nyrt. Triazolobenzazepinek
TW201938171A (zh) 2017-12-15 2019-10-01 匈牙利商羅特格登公司 作為血管升壓素Ｖ１ａ受體拮抗劑之三環化合物
JP2023546527A (ja) * 2020-11-26 2023-11-02 シャンハイ ジェミンケア ファーマシューティカル カンパニー，リミティド 新規ベンズアゼピンスピロ環式誘導体

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US5011628A (en) * 1988-06-15 1991-04-30 Givaudan Corporation N,N'-diarylbenzamidines useful as ultraviolet light absorbers
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JP2905909B2 (ja) * 1991-04-19 1999-06-14 大塚製薬株式会社 バソプレシン拮抗剤
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JPH03255077A (ja) * 1990-03-01 1991-11-13 Taiji Nakayama ピリミジン誘導体およびそれを有効成分とする血小板凝集阻止剤
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JP3255077B2 (ja) * 1997-04-23 2002-02-12 日本電気株式会社 電話機

Also Published As

Publication number Publication date
NO960231L (no) 1996-03-21
EP0709386A1 (fr) 1996-05-01
EP0709386B1 (fr) 2003-05-07
PL312654A1 (en) 1996-04-29
DE69432632T2 (de) 2004-02-19
ES2228405T3 (es) 2005-04-16
DE69432632D1 (de) 2003-06-12
ES2198418T3 (es) 2004-02-01
FI960260A0 (fi) 1996-01-19
NZ268671A (en) 1997-09-22
AU3990697A (en) 1997-12-18
AU683483B2 (en) 1997-11-13
CA2167673C (fr) 2004-09-21
FI960260A (fi) 1996-01-19
ATE239726T1 (de) 2003-05-15
CN1127508A (zh) 1996-07-24
KR960703917A (ko) 1996-08-31
ATE277003T1 (de) 2004-10-15
AU7195794A (en) 1995-02-20
HU9600102D0 (en) 1996-03-28
CN1040210C (zh) 1998-10-14
EP1097920A1 (fr) 2001-05-09
WO1995003305A1 (fr) 1995-02-02
KR100304331B1 (ko) 2001-11-22
CA2167673A1 (fr) 1995-02-02
NO960231D0 (no) 1996-01-19
UA64690C2 (en) 2004-03-15
US5723606A (en) 1998-03-03
US5856564A (en) 1999-01-05
EP0709386A4 (fr) 1997-06-25
DE69434032T2 (de) 2005-09-22
PL177738B1 (pl) 2000-01-31
HUT74582A (en) 1997-01-28
EP1097920B1 (fr) 2004-09-22
RU2129123C1 (ru) 1999-04-20
NO306303B1 (no) 1999-10-18
TW279163B (fr) 1996-06-21
DE69434032D1 (de) 2004-10-28

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