KR900009596A - N-피리디닐-9h-카바졸-9-아민, 이의 제조방법 및 이의 약제로서의 용도 - Google Patents
N-피리디닐-9h-카바졸-9-아민, 이의 제조방법 및 이의 약제로서의 용도 Download PDFInfo
- Publication number
- KR900009596A KR900009596A KR1019890019472A KR890019472A KR900009596A KR 900009596 A KR900009596 A KR 900009596A KR 1019890019472 A KR1019890019472 A KR 1019890019472A KR 890019472 A KR890019472 A KR 890019472A KR 900009596 A KR900009596 A KR 900009596A
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- compound
- lower alkyl
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Hydrogenated Pyridines (AREA)
- Indole Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (11)
- 하기 일반식(Ⅰ)의 화합물 또는 이의 약제학적으로 허용되는 산 부가염.상기식에서, X는 수소, 저급 알킬, 저급 알콕시 또는 할로겐이며; Y는 수소, 저급 알킬 또는 할로겐이고; Z는 수소, 저급 알킬, 또는 할로겐이며; R은 수소, 저급 알킬, 저급 알케닐, 저급 알킬카보닐, 디메틸아미노저급 알킬 또는(여기서, m은 1 내지 6의 정수이다)이고, 단, R이 저급 알케닐인 경우 이중 결합은 질소원자에 대해 알파가 아니다.
- 제1항에 있어서, X가 수소 또는 할로겐이고, Y가 수소 또는 할로겐이며, Z가 수소인 화합물.
- 제2항에 있어서, R이 수소, 저급 알킬 또는 저급 알케닐인 화합물.
- 제1항에 있어서, N-(4-피리디닐)-9H-카바졸-9-아민 또는 이의 약제학적으로 허용되는 산 부가염인 화합물.
- 제1항에 있어서, N-메틸-N-(4-피리디닐)-9H-카바졸-9-아민 또는 이의 약제학적으로 허용되는 산 부가염인 화합물.
- 제1항에 있어서, N-에틸-N-(4-피리디닐)-9H-카바졸-9-아민 또는 이의 약제학적으로 허용되는 산 부가염인 화합물.
- 제1항에 있어서, N-(프로필)-N-(4-피리디닐)-9H-카바졸-9-아민 또는 이의 약제학적으로 허용되는 산 부가염인 화합물.
- 제1항에 있어서, 3-브로모-N-(4-피리디닐)-9H-카바졸-9-아민 또는 이의 약제학적으로 허용되는 산 부가염인 화합물.
- 활성성분인 제1항에서 정의한 화합물 및 적절한 담체를 포함하는 약제학적 조성물.
- 진통, 진경, 항우울 및/또는 기억증진 활성을 가지는 약제를 제조하기 위한, 제1항에서 정의한 화합물의 용도.
- a) 하기 일반식(Ⅱ)의 화합물을 하기 일반식(Ⅲ)의 화합물과 반응시켜 R이 수소 또는 저급 알킬인 일반식(Ⅰ)의 화합물을 수득하고, b) 임의로, R이 수소인 일반식(Ⅰ)의 화합물을 강염기의 존재하에서 일반식 R2W(여기서, W는 염소 또는 브롬이고, R2는 저급 알킬, 저급 알케닐 또는 디메틸아미노 저급 알킬이다)의 화합물과 반응시켜, R이 저급 알킬, 저급 알케닐 또는 디메틸아미노저급 알킬인 일반식(Ⅰ)의 화합물을 수득하거나, c) 임의로, R이 수소인 일반식(Ⅰ)의 화합물을 일반식(R30)2S02(여기서, R3은 저급 알킬이다) 또는 일반식 R4OSO2C6H4CH3(여기서, R4는 저급 알킬또는 래디칼 -(CH2)r-이다)의 화합물과 반응시켜 R이 저급 알킬 또는 래디칼-(CH2)r-인 일반식(Ⅰ)의 화합물을 수득하거나, 또는 d) 임의로, R이 수소인 일반식(Ⅰ)의 화합물을 임의로 일반식 R5-CO-CI (여기서, R5는 저급 알킬이다)의 알카노일클로라이드와 반응시켜, R이 저급 알킬카보닐인 일반식(Ⅰ)의 화합물을 수득한 후, 임의로 통상적인 방법에 따라 이의 약제학적으로 허용되는 산 부가염을 제조함을 특징으로 하여, 하기 일반식(Ⅰ)의 화합물을 제조하는 방법.상기식에서, X는 수소, 저급 알킬, 저급 알콕시 또는 할로겐이며; Y는 수소, 저급 알킬 또는 할로겐이고; Z는 수소, 저급 알킬 또는 할로겐이며; R는 수소, 저급 알킬, 저급 알케닐, 저급 알킬카보닐, 디메틸아미노저급 알킬 또는 -(CH2)m-(여기서, m은 1 내지 6의 정수이다)이고 R1은 수소 또는 저급 알킬이며, 단. R이 저급 알케닐인 경우 이중 결합은 질소원자에 대해 알파가 아니다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/289,887 US4868190A (en) | 1988-12-27 | 1988-12-27 | N-pyridinyl-9H-carbazol-9-amines |
| US289887 | 1988-12-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR900009596A true KR900009596A (ko) | 1990-07-05 |
Family
ID=23113557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019890019472A Withdrawn KR900009596A (ko) | 1988-12-27 | 1989-12-26 | N-피리디닐-9h-카바졸-9-아민, 이의 제조방법 및 이의 약제로서의 용도 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4868190A (ko) |
| EP (1) | EP0376155B1 (ko) |
| JP (1) | JPH0725749B2 (ko) |
| KR (1) | KR900009596A (ko) |
| AT (1) | ATE79118T1 (ko) |
| AU (1) | AU623205B2 (ko) |
| CA (1) | CA2006529C (ko) |
| DE (1) | DE68902386T2 (ko) |
| DK (1) | DK662189A (ko) |
| ES (1) | ES2044043T3 (ko) |
| FI (1) | FI896243A7 (ko) |
| GR (1) | GR3006140T3 (ko) |
| IE (1) | IE894175L (ko) |
| IL (1) | IL92867A0 (ko) |
| NO (1) | NO895222L (ko) |
| NZ (1) | NZ231943A (ko) |
| PH (1) | PH27122A (ko) |
| PT (1) | PT92696A (ko) |
| ZA (1) | ZA899904B (ko) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4916135A (en) * | 1989-05-08 | 1990-04-10 | Hoechst Roussel Pharmaceuticals Inc. | N-heteroaryl-4-quinolinamines |
| FI95466C (fi) * | 1989-08-02 | 1996-02-12 | Hoechst Roussel Pharma | Menetelmä terapeuttisesti aktiivisten 2,3-dihydro-1-(pyridyyliamino)indolien valmistamiseksi |
| US4994472A (en) * | 1989-08-02 | 1991-02-19 | Hoechst-Roussel Pharmaceuticals Incorporated | 1-(pyridinylamino)-2-pyrrolidinones as pain relievers |
| US5179099A (en) * | 1989-08-02 | 1993-01-12 | Hoechst-Roussel Pharmaceuticals Incorporated | 2,3-dihydro-1-(pyridinylamino)-indoles |
| US4983608A (en) * | 1989-09-05 | 1991-01-08 | Hoechst-Roussell Pharmaceuticals, Inc. | N-substituted-4-pyrimidinamines and pyrimidinediamines |
| DK0840609T3 (da) * | 1995-07-27 | 2002-09-30 | Aventis Pharma Inc | Anvendelse af usubstituerede og substituerede N-(pyrrol-1-yl)pyridinaminer som antikonvulsive midler |
| HUP9802413A3 (en) * | 1995-07-27 | 2002-02-28 | Aventis Pharmaceuticals Inc Br | Use of n-(pyrrol-1-yl)pyridinamines as anticonvulsant agents and for the preparation of a pharmaceutical composition for the treatment of convulsions |
| ZA989365B (en) * | 1997-10-15 | 1999-04-15 | Boehringer Mannheim Pharm Corp | Preparation for treating alzheimer's disease |
| CZ2003445A3 (cs) * | 2000-07-21 | 2004-08-18 | Ortho@Mcneilápharmaceuticalźáinc | Karbamátové sloučeniny pro prevenci nebo léčbu neuropatické bolesti a bolesti asociované s histaminovou a migrenózní bolestí hlavy |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH475982A (de) * | 1966-11-16 | 1969-07-31 | Wander Ag Dr A | Verfahren zur Herstellung von Carbazolderivaten |
| EP0073849A1 (en) * | 1981-09-03 | 1983-03-16 | Schering Corporation | Novel phenyl-1,2,3,4-tetrahydrocarbazoles, their preparation and pharmaceutical compositions containing them |
| US4752610A (en) * | 1985-12-04 | 1988-06-21 | Hoechst-Roussel Pharmaceuticals Inc. | N-(pyrrol-1-yl)pyridinamines having memory enhancing properties |
| US4792562A (en) * | 1985-12-04 | 1988-12-20 | Hoechst-Roussel Pharmaceuticals, Inc. | N-(pyrrol-1-yl)pyridinamines having memory enhancing activity |
| EP0287982B1 (en) * | 1987-04-24 | 1994-12-07 | Hoechst-Roussel Pharmaceuticals Incorporated | N-(Pyridinyl)-1H-indol-1-amines, a process for their preparation and their use as medicaments |
| US4806554A (en) * | 1988-01-11 | 1989-02-21 | Hoechst-Roussel Pharmaceuticals, Inc. | Pyrazol and indazolpyridinamines |
| US4916135A (en) * | 1989-05-08 | 1990-04-10 | Hoechst Roussel Pharmaceuticals Inc. | N-heteroaryl-4-quinolinamines |
| FI95466C (fi) * | 1989-08-02 | 1996-02-12 | Hoechst Roussel Pharma | Menetelmä terapeuttisesti aktiivisten 2,3-dihydro-1-(pyridyyliamino)indolien valmistamiseksi |
| US5006537A (en) * | 1989-08-02 | 1991-04-09 | Hoechst-Roussel Pharmaceuticals, Inc. | 1,3-dihydro-1-(pyridinylamino)-2H-indol-2-ones |
-
1988
- 1988-12-27 US US07/289,887 patent/US4868190A/en not_active Expired - Lifetime
-
1989
- 1989-12-21 IE IE894175A patent/IE894175L/xx unknown
- 1989-12-21 EP EP89123612A patent/EP0376155B1/en not_active Expired - Lifetime
- 1989-12-21 ES ES89123612T patent/ES2044043T3/es not_active Expired - Lifetime
- 1989-12-21 NZ NZ231943A patent/NZ231943A/en unknown
- 1989-12-21 DE DE8989123612T patent/DE68902386T2/de not_active Expired - Fee Related
- 1989-12-21 AT AT89123612T patent/ATE79118T1/de not_active IP Right Cessation
- 1989-12-22 PT PT92696A patent/PT92696A/pt unknown
- 1989-12-22 DK DK662189A patent/DK662189A/da not_active Application Discontinuation
- 1989-12-22 FI FI896243A patent/FI896243A7/fi not_active Application Discontinuation
- 1989-12-22 AU AU47203/89A patent/AU623205B2/en not_active Ceased
- 1989-12-22 CA CA002006529A patent/CA2006529C/en not_active Expired - Fee Related
- 1989-12-22 NO NO89895222A patent/NO895222L/no unknown
- 1989-12-25 IL IL92867A patent/IL92867A0/xx unknown
- 1989-12-26 KR KR1019890019472A patent/KR900009596A/ko not_active Withdrawn
- 1989-12-26 PH PH39801A patent/PH27122A/en unknown
- 1989-12-26 JP JP1335256A patent/JPH0725749B2/ja not_active Expired - Fee Related
- 1989-12-27 ZA ZA899904A patent/ZA899904B/xx unknown
-
1992
- 1992-11-04 GR GR920402184T patent/GR3006140T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2006529A1 (en) | 1990-06-27 |
| ES2044043T3 (es) | 1994-01-01 |
| US4868190A (en) | 1989-09-19 |
| JPH02247173A (ja) | 1990-10-02 |
| DK662189A (da) | 1990-06-28 |
| AU623205B2 (en) | 1992-05-07 |
| ATE79118T1 (de) | 1992-08-15 |
| EP0376155A1 (en) | 1990-07-04 |
| ZA899904B (en) | 1991-02-27 |
| AU4720389A (en) | 1990-07-05 |
| IL92867A0 (en) | 1990-09-17 |
| NZ231943A (en) | 1992-06-25 |
| FI896243A7 (fi) | 1990-06-28 |
| DE68902386D1 (de) | 1992-09-10 |
| CA2006529C (en) | 1999-08-10 |
| PT92696A (pt) | 1990-06-29 |
| PH27122A (en) | 1993-03-16 |
| NO895222L (no) | 1990-06-28 |
| IE894175L (en) | 1990-06-27 |
| GR3006140T3 (ko) | 1993-06-21 |
| DK662189D0 (da) | 1989-12-22 |
| FI896243A0 (fi) | 1989-12-22 |
| NO895222D0 (no) | 1989-12-22 |
| DE68902386T2 (de) | 1993-02-11 |
| EP0376155B1 (en) | 1992-08-05 |
| JPH0725749B2 (ja) | 1995-03-22 |
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