KR900001684A - (1-히드록시-2- 피페리딜알킬)-인돌-2-온, 2-퀴놀리논, 2- 벤조[b] 아자피논, 벤즈이미다졸-2-온 및 퀴나졸린-2-온의 유도체, 그의 제조 및 치료요법에서의 그의 적용 - Google Patents
(1-히드록시-2- 피페리딜알킬)-인돌-2-온, 2-퀴놀리논, 2- 벤조[b] 아자피논, 벤즈이미다졸-2-온 및 퀴나졸린-2-온의 유도체, 그의 제조 및 치료요법에서의 그의 적용 Download PDFInfo
- Publication number
- KR900001684A KR900001684A KR1019890009861A KR890009861A KR900001684A KR 900001684 A KR900001684 A KR 900001684A KR 1019890009861 A KR1019890009861 A KR 1019890009861A KR 890009861 A KR890009861 A KR 890009861A KR 900001684 A KR900001684 A KR 900001684A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- compound according
- methyl group
- halogen atom
- hydrogen atom
- Prior art date
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
- A61P25/28—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
- A61P35/00—Antineoplastic agents
-
- 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
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (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)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Furan Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 일반식(I)에 해당하는 순수한 광학 이성질체 또는 그 혼합물 형태의 화합물 및 약리학적으로 허용되는 산과의 부가염.상기식에서,Z는 -CH2-,C(CH3)2-, -CH=CH-, -(CH2)2-, -(CH2)3-, -NH- 또는 -N(CH3)CH2-(여기서 질소원자는 카르보닐기에 결합되어 있다)인 식의 기를 나타내고, R1은 수소원자 또는 C1-C4알칼기를 나타내고, R2는 수소원자 또는 메틸기를 나타내고, R3는 할롤겐원자 또는 메틸기로 치환될 수 있는 페녹시기, 또는 나프틸옥시기, 또는 할로겐원자 또는 메틸기로 치환될 수 있는 페닐메틸기, 또는 Z가 -CH=CH-또는 -(CH2)2-인 식의 기를 나타내지 않을때 치환되지 않은 페닐메틸기, 또는 비스(4-플루오로페닐)메틸기, 또는 할로겐원자 또는 메틸기로 치환될 수 있는 페닐메톡시기, 또는 (2-나프틸)메톡시기, 또는 할로겐원자 또는 메틸기로 치환될 수 있는 페녹시메틸기, 또는 피리디닐옥시기이고, R4는 수소원자를 나타내고, 또는 더욱이, R3와 R4가 함께, 그리고 피페리딘 링고 같이 스피로(2,3-디히드로 벤조푸란-2,4′-피페리드-1-일)기를 형성한다.
- 제 1 항에 있어서, Z가 -CH2- 를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, Z가C(CH3)2-를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, Z가 -CH=CH-를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, Z가 -(CH2)2-를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, Z가 -(CH2)3-를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, Z가 -NH- 를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 있어서, -N(CH3)CH2-를 나타내는 것을 특징으로 하는 화합물.
- 제 1 항에 따른 화합물의 제조방법에 있어서, 다음 일반식(II)(상기식에서, Z,R1과 R2는 제 1 항에서 정의한 것과 같고 X는 염소 또는 브롬과 같은 할로겐원자를 나타낸다)의 할로겐화 케톤이 탄산나트륨 또는 탄산칼륨과 같은 무기염기 존재하에서 또는 과량의 일반식(III)의 피페리딘의 존재하에서, 저급알코올 또는 아세토니트릴과 같은 용매속에서, 그리고 필요하다면 물의 존재하에서 가장 먼저 일반식(III)(상기식에서 R3와 R4는 제 1 항에서 정의한 것과 같다)의 피페리딘과 반응하고, 이와같이 얻어진 일반식(IV)의 케톤이 알칼리 또는 산 매질속에서 수소화 붕소나타륨 또는 수소화 붕소칼륨에 의해 환원되는 것을 특징으로 하는 방법.
- 제 1 항에 따른 화합물을 함유하는 것을 특징으로 하는 약학적 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8809449A FR2634206B1 (fr) | 1988-07-12 | 1988-07-12 | Derives de (hydroxy-1 piperidinyl-2 alkyl) indolones-2 et quinoleinones-2, leur preparation et leur application en therapeutique |
FR88/16373 | 1988-07-12 | ||
FR88/09449 | 1988-07-12 | ||
FR888816373A FR2640266B2 (fr) | 1988-07-12 | 1988-12-13 | Derives de (hydroxy-1 piperidinyl-2 alkyl) indolones-2, quinoleinones-2, benzo(b)azepinones-2 et benzimidazolones-2, leur preparation et leur application en therapeutique |
Publications (1)
Publication Number | Publication Date |
---|---|
KR900001684A true KR900001684A (ko) | 1990-02-27 |
Family
ID=26226791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890009861A KR900001684A (ko) | 1988-07-12 | 1989-07-11 | (1-히드록시-2- 피페리딜알킬)-인돌-2-온, 2-퀴놀리논, 2- 벤조[b] 아자피논, 벤즈이미다졸-2-온 및 퀴나졸린-2-온의 유도체, 그의 제조 및 치료요법에서의 그의 적용 |
Country Status (18)
Country | Link |
---|---|
US (1) | US5034401A (ko) |
EP (1) | EP0351282B1 (ko) |
JP (1) | JPH0272173A (ko) |
KR (1) | KR900001684A (ko) |
AT (1) | ATE96437T1 (ko) |
AU (1) | AU618378B2 (ko) |
CA (1) | CA1317292C (ko) |
DE (1) | DE68910210T2 (ko) |
DK (1) | DK341989A (ko) |
ES (1) | ES2062064T3 (ko) |
FI (1) | FI93012C (ko) |
FR (1) | FR2640266B2 (ko) |
HU (1) | HU201544B (ko) |
IE (1) | IE62216B1 (ko) |
IL (1) | IL90908A0 (ko) |
NO (1) | NO174100C (ko) |
NZ (1) | NZ229903A (ko) |
PT (1) | PT91126B (ko) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5182278A (en) * | 1989-02-28 | 1993-01-26 | Adir Et Compagnie | Analgesic benzoxazolinones having at the 6-position a 1-hydroxy-3-morpholinopropyl side chain |
CA2023492A1 (en) * | 1989-08-31 | 1991-03-01 | Barry Clifford Lange | Herbicidal glutarimides |
DK0554247T3 (da) * | 1990-05-10 | 2000-08-07 | Pfizer | Neurobeskyttende indolon og beslægtede derivater |
JP2807577B2 (ja) * | 1990-06-15 | 1998-10-08 | エーザイ株式会社 | 環状アミド誘導体 |
FR2668149B1 (fr) * | 1990-10-18 | 1994-09-23 | Synthelabo | Le 1-(3,4-dihydro-2-oxo-1h-quinolein-6-yl)-2-[4-(2-phenyl-ethyl)piperidin-1-yl]ethanol, sa preparation et son application en therapeutique. |
TW197435B (ko) * | 1990-11-22 | 1993-01-01 | Takeda Pharm Industry Co Ltd | |
NZ243065A (en) * | 1991-06-13 | 1995-07-26 | Lundbeck & Co As H | Piperidine derivatives and pharmaceutical compositions |
EP0524846A1 (fr) * | 1991-06-27 | 1993-01-27 | Synthelabo | Dérivés de 2-(pipéridin-1-y1) éthanol, leur préparation et leur application en thérapeutique |
FR2678270B1 (fr) * | 1991-06-27 | 1995-01-13 | Synthelabo | Derives de 2-(piperidin-1-yl)ethanol, leur preparation et leur application en therapeutique. |
HUT70528A (en) * | 1991-07-17 | 1995-10-30 | Pfizer | 2-(4-hydroxypiperidino)-1-alkanol derivatives as antiischemic agents and process for production thereof |
TW263504B (ko) | 1991-10-03 | 1995-11-21 | Pfizer | |
FR2684379B1 (fr) * | 1991-12-02 | 1995-04-28 | Synthelabo | Derives de piperidine, leur preparation et leur application en therapeutique. |
US5462934A (en) * | 1992-03-09 | 1995-10-31 | Takeda Chemical Industries | Condensed heterocyclic ketone derivatives and their use |
TW218875B (ko) * | 1992-03-09 | 1994-01-11 | Takeda Pharm Industry Co Ltd | |
FR2688504B1 (fr) * | 1992-03-13 | 1995-05-05 | Synthelabo | Derives de 2-(piperidin-1-yl)ethanol, leur preparation et leur application en therapeutique. |
US6255322B1 (en) | 1992-06-19 | 2001-07-03 | Pfizer Inc. | 2-(4-hydroxypiperidino)-1-alkanol derivatives as antiischemic agents |
US5436255A (en) * | 1992-07-23 | 1995-07-25 | Pfizer Inc. | Method of treating diseases susceptable to treatment by blocking NMDA-receptors |
CZ280669B6 (cs) * | 1992-10-30 | 1996-03-13 | Pfizer Inc. | Deriváty 3,4-dihydro-2(1H)-chinolonu a farmaceutický prostředek na jejich bázi |
US5498610A (en) * | 1992-11-06 | 1996-03-12 | Pfizer Inc. | Neuroprotective indolone and related derivatives |
ATE183184T1 (de) * | 1994-01-31 | 1999-08-15 | Pfizer | Neuroprotektive chroman verbindungen |
ES2128629T3 (es) * | 1994-10-31 | 1999-05-16 | Merck Patent Gmbh | Derivados de bencilpiperidina con afinidad elevada a puntos de enlace de receptores de aminoacidos. |
FR2738568B1 (fr) * | 1995-09-08 | 1997-10-17 | Synthelabo | Derives de 4-(cycloalkyl)piperidines et 4-(cycloalkylalkyl) piperidines, leur preparation et leur application en therapeutique |
WO1997009309A1 (fr) * | 1995-09-08 | 1997-03-13 | Synthelabo | Derives de 4-(cycloalkyl)piperidines et de 4-(cycloalkylalkyl)pi peridines, leur preparation et leur application en therapeutique |
ZA9610745B (en) * | 1995-12-22 | 1997-06-24 | Warner Lambert Co | 4-Subsituted piperidine analogs and their use as subtype selective nmda receptor antagonists |
ZA9610741B (en) | 1995-12-22 | 1997-06-24 | Warner Lambert Co | 4-Substituted piperidine analogs and their use as subtype selective nmda receptor antagonists |
ZA9610736B (en) | 1995-12-22 | 1997-06-27 | Warner Lambert Co | 2-Substituted piperidine analogs and their use as subtypeselective nmda receptor antagonists |
ZA9610738B (en) | 1995-12-22 | 1997-06-24 | Warner Lambert Co | Subtype selective nmda receptor ligands and the use thereof |
CA2306477A1 (en) * | 1997-11-05 | 1999-05-20 | Neurosearch A/S | Azaring-ether derivatives and their use as nicotinic ach receptor modulators |
GB9725541D0 (en) * | 1997-12-02 | 1998-02-04 | Pharmacia & Upjohn Spa | Amino-benzothiazole derivatives |
AR033485A1 (es) * | 2001-09-25 | 2003-12-26 | Otsuka Pharma Co Ltd | Sustancia medicinal de aripiprazol de baja higroscopicidad y proceso para la preparacion de la misma |
NZ604423A (en) * | 2010-06-24 | 2015-01-30 | Alkermes Pharma Ireland Ltd | Prodrugs of nh-acidic compounds: ester, carbonate, carbamate and phosphonate derivatives |
MA41169A (fr) * | 2014-12-17 | 2017-10-24 | Acraf | Composés antibactériens à large spectre d'activité |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3217011A (en) * | 1965-05-07 | 1965-11-09 | Sterling Drug Inc | 1-(indolyglyoxalyl)-piperidines |
JPS51125291A (en) * | 1974-12-07 | 1976-11-01 | Otsuka Pharmaceut Co Ltd | A process for preparing novel carbostyryl derivatives |
JPS51118772A (en) * | 1975-04-09 | 1976-10-18 | Otsuka Pharmaceut Co Ltd | Method for preparing carbostyryl derivatives |
PH17194A (en) * | 1980-03-06 | 1984-06-19 | Otsuka Pharma Co Ltd | Novel carbostyril derivatives,and pharmaceutical composition containing the same |
FR2528043A1 (fr) * | 1982-06-03 | 1983-12-09 | Roussel Uclaf | Nouveaux derives de la 1,3-dihydro 4-/1-hydroxy-2-amino-ethyl/2h-indol-2-one, leurs sels, procede de preparation, application a titre de medicaments et compositions les renfermant |
FR2581993B1 (fr) * | 1985-05-14 | 1988-03-18 | Synthelabo | Derives de (benzoyl-4 piperidino)-2 phenyl-1 alcanols, leur preparation et leur application en therapeutique |
US4788201A (en) * | 1987-01-22 | 1988-11-29 | Hoechst-Roussel Pharmaceuticals Inc. | 3-methylenespiro (benzofuranpiperidines) |
-
1988
- 1988-12-13 FR FR888816373A patent/FR2640266B2/fr not_active Expired - Lifetime
-
1989
- 1989-07-03 EP EP89401898A patent/EP0351282B1/fr not_active Expired - Lifetime
- 1989-07-03 AT AT89401898T patent/ATE96437T1/de not_active IP Right Cessation
- 1989-07-03 DE DE89401898T patent/DE68910210T2/de not_active Expired - Fee Related
- 1989-07-03 ES ES89401898T patent/ES2062064T3/es not_active Expired - Lifetime
- 1989-07-10 IL IL90908A patent/IL90908A0/xx not_active IP Right Cessation
- 1989-07-11 NO NO892870A patent/NO174100C/no not_active IP Right Cessation
- 1989-07-11 CA CA000605386A patent/CA1317292C/en not_active Expired - Fee Related
- 1989-07-11 FI FI893365A patent/FI93012C/fi not_active IP Right Cessation
- 1989-07-11 HU HU893488A patent/HU201544B/hu not_active IP Right Cessation
- 1989-07-11 JP JP1180140A patent/JPH0272173A/ja active Pending
- 1989-07-11 AU AU38029/89A patent/AU618378B2/en not_active Ceased
- 1989-07-11 KR KR1019890009861A patent/KR900001684A/ko not_active Application Discontinuation
- 1989-07-11 NZ NZ229903A patent/NZ229903A/en unknown
- 1989-07-11 US US07/378,094 patent/US5034401A/en not_active Expired - Lifetime
- 1989-07-11 PT PT91126A patent/PT91126B/pt active IP Right Grant
- 1989-07-11 DK DK341989A patent/DK341989A/da not_active Application Discontinuation
- 1989-07-11 IE IE223789A patent/IE62216B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FI93012B (fi) | 1994-10-31 |
HU201544B (en) | 1990-11-28 |
NZ229903A (en) | 1991-04-26 |
DE68910210T2 (de) | 1994-05-11 |
PT91126B (pt) | 1994-12-30 |
AU3802989A (en) | 1990-01-18 |
CA1317292C (en) | 1993-05-04 |
ATE96437T1 (de) | 1993-11-15 |
ES2062064T3 (es) | 1994-12-16 |
FI93012C (fi) | 1995-02-10 |
FR2640266B2 (fr) | 1992-07-10 |
DK341989A (da) | 1990-04-25 |
JPH0272173A (ja) | 1990-03-12 |
NO892870L (no) | 1990-01-15 |
FI893365A (fi) | 1990-01-13 |
US5034401A (en) | 1991-07-23 |
PT91126A (pt) | 1990-02-08 |
EP0351282B1 (fr) | 1993-10-27 |
DE68910210D1 (de) | 1993-12-02 |
IE892237L (en) | 1990-01-12 |
FI893365A0 (fi) | 1989-07-11 |
IE62216B1 (en) | 1995-01-11 |
DK341989D0 (da) | 1989-07-11 |
HUT50328A (en) | 1990-01-29 |
IL90908A0 (en) | 1990-02-09 |
AU618378B2 (en) | 1991-12-19 |
FR2640266A2 (fr) | 1990-06-15 |
NO892870D0 (no) | 1989-07-11 |
NO174100B (no) | 1993-12-06 |
NO174100C (no) | 1994-03-16 |
EP0351282A1 (fr) | 1990-01-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR900001684A (ko) | (1-히드록시-2- 피페리딜알킬)-인돌-2-온, 2-퀴놀리논, 2- 벤조[b] 아자피논, 벤즈이미다졸-2-온 및 퀴나졸린-2-온의 유도체, 그의 제조 및 치료요법에서의 그의 적용 | |
NO934740L (no) | Forbindinger vedrörende benzotiofener | |
SE423812B (sv) | Forfarande for framstellning av terapeutiskt aktiva derivat av azetidin-2-karboxylsyra, prolin och pipekolinsyra | |
KR880011135A (ko) | 콜린성계 상에 작용하는 신규 티아졸 유도체, 그의 제조방법 및 약학 조성물 | |
KR890002121A (ko) | 신규 벤조피란 유도체, 그의 제조방법 및 이를 함유하는 제약학적 조성물 | |
ATE239619T1 (de) | Aufzeichnungsmaterial sowie bilddruckverfahren das dieses material verwendet | |
DE69316068D1 (de) | 1-[2-(Arylsulfonylamino)-1-oxoethyl]piperidin-Derivate, ihre Herstellung und therapeutische Verwendung | |
EA200100310A1 (ru) | Кислородсодержащие гетероциклические соединения | |
ATE361283T1 (de) | Oxazolylarylpropionsäure derivate und ihre verwendung als ppar agonisten | |
ZA917606B (en) | Pharmaceutical azagranatane derivatives | |
NO910304D0 (no) | Nye leukotrien-b4-derivater, fremgangsmaate for deres fremstilling og deres anvendelse som legemiddel. | |
KR920004381A (ko) | 치환된 피리미딘 유도체, 이의 제조방법 및 약제로서의 이의 용도 | |
SE7703000L (sv) | Forfarande for framstellning av karbostyrilderivat | |
DE3876711D1 (de) | Piperidin-derivate, deren herstellung und deren verwendung als heilmittel. | |
FI883484A0 (fi) | Benzimidazolderivat, deras framstaellning och anvaendning vid terapi. | |
DE59206593D1 (de) | Verwendung von 2-Iminothiazolidin-4-onderivaten als neuartige Arzneimittelwirkstoffe | |
DK0411394T3 (da) | Imidazoquinolon-derivater | |
SE8703494D0 (sv) | Mellanprodukter anvendbara vid framstellning av 2-tiofen-ettiksyraderivat | |
ES8105981A1 (es) | Procedimiento para la preparacion de derivados de 4-(nafta- leniloxi)piperidina | |
KR840005092A (ko) | 벤조페논 유도체의 제조방법 | |
ES443357A1 (es) | Un procedimiento de preparacion de benzodioxanos-1,4. | |
SE8207294D0 (sv) | 1,4-tiazankarboxylsyraderivat, deras framstellning och anvendning och kompositioner vari dessa derivat ingar | |
KR830009000A (ko) | 2-벤조일아미노-치환벤질아민 유도체 및 그 제조방법 | |
KR920002574A (ko) | 6-(3-치환된 아미노프로피오닐)-7-데아세틸포르스콜린 유도체의 제조방법 | |
KR840003248A (ko) | 피란유도체와 그의 제조법 및 진드기 박멸제(殺壁蟲劑) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E601 | Decision to refuse application |