KR910002858A - 4H-인돌로[1,2-d][1,2,4]트리아졸로[4,3-a][1,4]벤조디아제핀, 이의 제조방법 및 약제로서의 용도 - Google Patents
4H-인돌로[1,2-d][1,2,4]트리아졸로[4,3-a][1,4]벤조디아제핀, 이의 제조방법 및 약제로서의 용도 Download PDFInfo
- Publication number
- KR910002858A KR910002858A KR1019900009914A KR900009914A KR910002858A KR 910002858 A KR910002858 A KR 910002858A KR 1019900009914 A KR1019900009914 A KR 1019900009914A KR 900009914 A KR900009914 A KR 900009914A KR 910002858 A KR910002858 A KR 910002858A
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- Prior art keywords
- compound
- formula
- halogen
- methyl
- indolo
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- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pain & Pain Management (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 하기 일반식(Ⅰ)의 화합물 또는 이의 약제학적으로 허용가능한 산부가염:상기식에서 X는 H, 할로겐, -OH, -OHC3, -NC2또는 -CF3이고; Y는 H, Cℓ 또는 Br이며: Z는 H, 할로겐, -OH 또는 -OCH3이고 ; R은 H, 저급 알킬, -CH2OH 또는 디저급 알킬아미노 메틸이다.
- 제1항에 있어서, X가 H 또는 할로겐이고, Z이 H인 화합물.
- 제2항에 있어서, R이 저급 알킬 또는 디저급 알킬 아미노메틸인 화합물.
- 제3항에 있어서, R이 메틸 또는 디메틸아미노 메틸인 화합물.
- 제1항에 있어서, 12-클로로-1-메틸-4H-인돌로[1,2-d][1,2,4]트리아졸로[4,3-a][1,4]벤조디아제핀 또는 이의 약제학적으로 허용 가능한 산부가염인 화합물.
- 제1항에 있어서, 10-클로로-1-메틸-4H-인돌로[1,2-d][1,2,4]트리아졸로[4,3-a][1,4]벤조디아제핀 또는 이의 약제학적으로 허용 가능한 산부가염인 화합물.
- 하기 일반식(Ⅵ)의 화합물:상기식에서 X는 H, 할로겐, -OH, -OCH3, -NO2또는 -CF3이고; Y는 H, Cℓ 또는 Br이며; Z는 H, 할로겐, -OH 또는 -CH3이다.
- 제1항에서 정의된 화합물 및 이를 위한 적합한 담체를 함유하는 약제학적 조성물.
- 진통 활성을 갖는 약제의 제조를 위한 화합물의 용도.
- 하기 일반식(Ⅵ)의 화합물을 하기 일반식(Ⅶ)의 화합물과 반응시키고, 임의로 Y가 수소인 일반식(Ⅰ)의 화합물을 N-클로로석신이미드 또는 N-브로모석신이미드와 반응시켜 Y가 Cℓ 또는 Br인 일반식(Ⅰ)의 화합물을 수득함을 특징으로 하여, 제1항에서 정의된 화합물을 제조하는 방법:상기식에서, X, Y, Z 및 R은 상기 정의한 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US375444 | 1989-07-03 | ||
US07/375,444 US4897392A (en) | 1989-07-03 | 1989-07-03 | 4H-indolo(1,2-d)(1,2,4)triazolo(4,3-A)(1,4)benzodiazepines |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910002858A true KR910002858A (ko) | 1991-02-26 |
Family
ID=23480913
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900009914A KR910002858A (ko) | 1989-07-03 | 1990-07-02 | 4H-인돌로[1,2-d][1,2,4]트리아졸로[4,3-a][1,4]벤조디아제핀, 이의 제조방법 및 약제로서의 용도 |
Country Status (13)
Country | Link |
---|---|
US (1) | US4897392A (ko) |
EP (1) | EP0406719A1 (ko) |
JP (1) | JPH0344392A (ko) |
KR (1) | KR910002858A (ko) |
AU (1) | AU5801490A (ko) |
CA (1) | CA2020297A1 (ko) |
FI (1) | FI903297A0 (ko) |
IE (1) | IE902393A1 (ko) |
IL (1) | IL94950A0 (ko) |
NO (1) | NO902934L (ko) |
NZ (1) | NZ234316A (ko) |
PT (1) | PT94567A (ko) |
ZA (1) | ZA905149B (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201311B (ko) * | 1991-06-17 | 1993-03-01 | Hoffmann La Roche | |
US6515122B1 (en) * | 1999-09-24 | 2003-02-04 | Lion Bioscience Ag | Tetracyclic benzimidazole derivatives and combinatorial libraries thereof |
BRPI0517412A (pt) * | 2004-10-12 | 2008-10-07 | Hoffmann La Roche | derivados de benzodiazepina substituìdos |
CA2584259C (en) * | 2004-10-20 | 2013-04-02 | F. Hoffmann-La Roche Ag | Imidazo-benzodiazepine derivatives |
EP1807432A1 (en) * | 2004-10-20 | 2007-07-18 | F. Hoffmann-Roche AG | Halogen substituted benzodiazepine derivatives |
CA2590333C (en) * | 2004-12-14 | 2013-01-08 | F. Hoffmann-La Roche Ag | Tetracyclic imidazo-benzodiazepines as gaba receptors modulators |
US8431568B2 (en) * | 2008-03-27 | 2013-04-30 | Bristol-Myers Squibb Company | Aromatic heterocyclic fused indolobenzadiazepine HCV NS5B inhibitors |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3375246A (en) * | 1965-06-11 | 1968-03-26 | Sandoz Ag | Isoindolines |
US3642778A (en) * | 1969-10-22 | 1972-02-15 | Robins Co Inc A H | Benzimidazo(1 2-d)(1 4)benzodiazepin-6(5h)-ones |
US3642779A (en) * | 1969-10-22 | 1972-02-15 | Robins Co Inc A H | Indolo(1 2-d)(1 4)benzodiazepin-6-ones |
US4013763A (en) * | 1974-07-12 | 1977-03-22 | Takeda Chemical Industries, Ltd. | Heterocyclic compounds |
JPS5572177A (en) * | 1978-11-27 | 1980-05-30 | Shionogi & Co Ltd | 4,1-benzoxazepine or 4,1-benzothiazepine |
US4587244A (en) * | 1984-04-11 | 1986-05-06 | Mcneilab, Inc. | Amidine benzodiazepines, methods for their use and intermediates |
US4596799A (en) * | 1985-01-29 | 1986-06-24 | Ciba-Geigy Corporation | 9H-pyrrolo[2,1-c]-1,2,4-triazolo[4,3-a][1,4]benzodiazepines |
US4737496A (en) * | 1986-10-01 | 1988-04-12 | Ciba-Geigy Corporation | 1,3,4,16b-tetrahydro-2H,10H-indolo[2,1-c]pyrazino-[1,2-a][1,4]benzodiazepines useful as serotonin-2 receptor antagonists |
-
1989
- 1989-07-03 US US07/375,444 patent/US4897392A/en not_active Expired - Fee Related
-
1990
- 1990-06-29 IE IE239390A patent/IE902393A1/en unknown
- 1990-06-29 EP EP90112436A patent/EP0406719A1/en not_active Withdrawn
- 1990-06-29 NZ NZ234316A patent/NZ234316A/en unknown
- 1990-06-29 FI FI903297A patent/FI903297A0/fi not_active Application Discontinuation
- 1990-07-02 PT PT94567A patent/PT94567A/pt not_active Application Discontinuation
- 1990-07-02 IL IL94950A patent/IL94950A0/xx unknown
- 1990-07-02 ZA ZA905149A patent/ZA905149B/xx unknown
- 1990-07-02 AU AU58014/90A patent/AU5801490A/en not_active Abandoned
- 1990-07-02 KR KR1019900009914A patent/KR910002858A/ko not_active Application Discontinuation
- 1990-07-02 NO NO90902934A patent/NO902934L/no unknown
- 1990-07-02 JP JP2172848A patent/JPH0344392A/ja active Pending
- 1990-07-03 CA CA002020297A patent/CA2020297A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
IE902393A1 (en) | 1991-06-19 |
PT94567A (pt) | 1991-03-20 |
EP0406719A1 (en) | 1991-01-09 |
US4897392A (en) | 1990-01-30 |
IL94950A0 (en) | 1991-06-10 |
NZ234316A (en) | 1992-03-26 |
NO902934L (no) | 1991-01-04 |
JPH0344392A (ja) | 1991-02-26 |
CA2020297A1 (en) | 1991-01-04 |
AU5801490A (en) | 1991-01-03 |
ZA905149B (en) | 1991-04-24 |
FI903297A0 (fi) | 1990-06-29 |
NO902934D0 (no) | 1990-07-02 |
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