KR920019730A - 시클로알킬 우레아 화합물 - Google Patents
시클로알킬 우레아 화합물 Download PDFInfo
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Abstract
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Claims (7)
- 하기일반식[I]의 시클로알킬 우레아 화합물(I) 또는 그의 약제학적으로 허용가능한 염 :상기식에서, R1은 하기식(a)의 기 :(상기식중, R6, R7및 R8은 동일 또는 상이하고, 그 각각은 수소 또는 탄소수 1∼8인 알킬이며, 단, R6, R7및 R8의 둘 또는 셋이 수소인 화합물은 제외된다), 할로알킬, 시클로알킬, 탄소수 1∼5인 알콕시, 페닐, 아르알킬 또는 헤테로알릴 ; 또는 탄소수 1∼4인 알킬, 탄소수 1∼8인 알콕시, 시클로알킬, 시클로알킬옥시, 할로알킬, 할로알콕시, 할로겐, 니트로, 아미노 및 치환된 아미노에서 선택된 1∼3개의 치환체로 방향족 고리가 각각 치환된 페닐, 아르알킬 또는 헤테로아릴이며 ; R2는 수소, 페닐 또는 탄소수 1∼4인 알킬, 탄소수 1∼4인 알콕시, 할로알킬 및 할로겐에서 선택되는 1∼3개의 치환체로 치환된 페닐이고, 상기 R1및 R2는 시클로알킬 고리의 동일한 탄소상에 치환되어 있어도 무방하고 ; R1및 R2는 함께 탄소수 3∼7인 치환 또는 비치환 시클릭탄화수소 또는 치환 또는 비치환 스피란을 형성할 수 있으며 ; R3은 수소, 탄소수 1∼8인 알킬, 시킬로알킬, 시클로알킬알킬, 알콕시알킬, 알킬티오알킬, 알킬렌디옥시로 치환된 아르알킬, 아르알킬옥시알킬 ; 탄소수 1∼4인 알킬, 탄소수 1∼5인 알콕시, 할로겐, 니트로, 히드록시, 아미노, 치환된 아미노, 할로알킬, 알킬티오, 벤질옥시 및 벤질티오에서 선택된 1∼3개의 치환체로 각각의 방향족 고리가 치환된 아르알킬 또는 아르알킬옥시, 헤테로아릴알킬, 페녹시알킬 또는 할로겐, 탄소수 1∼4일 알킬, 탄소수 1∼4인 알콕시, 니트로, 아미노 및 할로알킬에서 선택된 1∼3개의 치환체로 각각의 방향족 고리가 치환된 헤테로 아릴알킬 또는 페녹시알킬, 또는 하기식(c) 또는 (d)의 기 :(상기중에서 m은 1 또는 2이고 R11은 수소 또는 탄소수 1∼4인 알킬이며, R12는 수소탄소수 1∼4인 알킬 또는 아르알킬이다)이고 ; R4는 탄소수 1∼4인 알킬, 탄소수 1∼4인 알콕시, 할로알킬, 할로겐, 아미노 및 치환된 아미노에서 선택되는 1∼3개의 치환체로 치환된 페닐이며 ; n은 1,2 또는 3이다.
- 제1항에 있어서, R1이 페닐 또는 탄소수 1∼4인 알킬, 탄소수 1∼8인 알콕시, 할로알킬, 할로겐, 니트로, 아미노 및 치환된 아미노에서 선택된 1∼3개의 치환체로 치환된 페닐이고 ; R2는 페닐 또는 탄소수 1∼4인 알킬, 탄소수 1∼4인 알콕시, 트리플루오로메틸 및 할로겐에서 선택된 1∼3개의 치환체로 치환된 페닐이고, 상기 R1및 R3가 시킬로알킬 고리의 동일한 탄소상에 치환되어 있어도 무방하고 ; 또는 R1및 R2는 치환 또는 비치환된 탄소수 3∼7의 시클릭탄화수소를 형성하거나 치환 또는 비치환된 스피란을 형성해도 무방하며 ; R3는 수소, 탄소수 1∼8인 알킬, 시클로알킬, 시크로알킬알킬, 알킬티오, 알키렌 디옥시로 치환된 아르알킬, 아르알킬; 탄소수 1∼4 알킬, 탄소수 1∼5인 알콕시, 할로겐, 니트로, 할로알킬, 알킬티오, 벤질옥시 및 벤질티오에서 선택된 1∼3개의 치환체로 방향족 고리가 치환된 아르알킬 ; 또는 헤테로 아릴알킬이고 ; R4는 탄소수 1∼4인 알킬, 탄소수 1∼4인 알콕시, 트리플루오로메틸, 할로겐 및 치환된 아미노에서 선택된 1∼3개의 치환체로 치환된 페닐이며 ; n이 2인 화합물 또는 그의 약제학적으로 허용가능한 염.
- 제1항에 있어서, R1이 탄소수 3∼5인 2차 또는 3차 알킬, 시클로알킬 또는 페닐이고 ; R2는 수소이며 : R3는 수소, 탄소수 1∼8인 알킬, 시클로알킬, 시클로알킬알킬, 알킬렌디옥시로 치환된 아르알킬, 아르알킬 ; 탄소수 1∼4인 알킬, 탄소수 1∼5인 알콕시, 할로겐, 니트로, 히드록시, 할로알킬, 알킬티오, 벤질옥시 및 벤질티오에서 선택된 1∼3개의 치환체로 방향족 고리가 치환된 아르알킬, 또는 헤테로아릴알킬이고 ; R4는 탄소수 9인 알킬, 탄소수 1∼4인 알콕시 및 할로겐에서 선택된 1∼3개의 치환체로 치환된 페닐이며 ; n이 2인 화합물 또는 그의 약제학적으로 허용가능한 염.
- 제1항에 있어서, N-(2,6-디이소프로필페닐)-N'-(2-페닐시클로헥실)우레아, N-(2,6-디이소프로필페닐)-N'-헵틸-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-벤질-N'-(4-페닐시클로헥실)-우레아, N-(2,6-디에틸페닐)-N'-벤질-N'-(4-페닐시클로헥실)우레아, N-(2,4-디플루오로페닐)-N'-벤질-N'-(4-페닐시클로헥실)우레아, N-(2,4-디이소프로필페닐)-N'-(3,4-디메톡시벤질)-N'-(4-페닐시클로)우레아, N-(2,4,6-트리메톡시페닐)-N'-벤질-N'-(4-페닐시클로헥실)우레아, N-(2,6-디이소프로필페닐)-N'-벤질-N'-(4-t-부틸시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(2-메틸벤질)-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(2-클로로벤질)-N'-(4-페닐시클로헥실)우레아, N-(2,6-디이소프로필페닐)-N'-(2-페닐에틸)-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(3-페닐프로필)-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(1,1'-비시클로헥실-4-일)우레아, 트랜스-N-(2,6-디에틸페닐)-N'-시클로헥실메틸-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-시클로헥실메틸-N'-(4-페닐시클로헥실)우레아, N-(2,6-디이소프로필페닐)-N'-테닐-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-프르푸릴-N'-(4-페닐시클로헥실)우레아, N-(2,6-디에틸페닐)-N'-(2-메틸벤질)-N'-(4-페닐시클로헥실)우레아, N-(2,6-디에틸페닐)-N'-(2-클로로벤질)-N'-(4-페닐시클로헥실)우레아 및 트랜스-N-(2,6-디이소프로필페닐)-N'-(2-피리딜메틸)N'-(4-페닐시클로헥실)우레아로 구성된 군에서 선택되는 화합물 그의 약제학적으로 허용가능한 염.
- 제1항에 있어서, 트랜스-N-(2,6-디이소프로필페닐)-N'-벤질-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(2-메틸벤질)-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디이소프로필페닐)-N'-(2-클로로벤질)-N'-(4-페닐시클로헥실)우레아, 트랜스-N-(2,6-디에틸페닐)-N'-시클로헥실메틸-N'-(4-페닐시클로헥실)우레아로 구성된 군에서 선택되는 화합물 또는 그의 약제학적으로 허용가능한 염.
- 제1항에 있어서, N-(2,6-디이소프로필테닐)-N'-(4,4-디페닐시클로헥실)우레아인 화합물 또는 그의 약제학적으로 허용가능한 염.
- 제1항에 기재된 바와같은 화합물 그의 약제학적으로 허용가능한 염의 유효량 및 약제학적 담체로 구성된 약제학적 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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JP91-100450 | 1991-04-04 | ||
JP10045091 | 1991-04-04 | ||
JP19486991 | 1991-07-08 | ||
JP91-194869 | 1991-07-08 | ||
JP91-348898 | 1991-12-04 | ||
JP34889891 | 1991-12-04 |
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KR920019730A true KR920019730A (ko) | 1992-11-19 |
KR940011151B1 KR940011151B1 (ko) | 1994-11-24 |
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EP (1) | EP0507291A1 (ko) |
KR (1) | KR940011151B1 (ko) |
CA (1) | CA2065086A1 (ko) |
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TW (1) | TW209868B (ko) |
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CA2197364A1 (en) * | 1996-02-15 | 1997-08-16 | Toshikazu Suzuki | Phenol compound and process for preparing the same |
SE9802209D0 (sv) | 1998-06-22 | 1998-06-22 | Astra Pharma Inc | Novel compounds |
FR2781222A1 (fr) * | 1998-07-17 | 2000-01-21 | Lipha | Composes cycliques utilisables dans le traitement de dyslipidemies, de l'atherosclerose et du diabete, compositions pharmaceutiques les contenant et procede de preparation |
AU2001255620A1 (en) | 2000-04-26 | 2001-11-07 | Warner-Lambert Company | Cyclohexylamine derivative as subtype selective NMDA receptor antagonists |
WO2003047568A1 (en) | 2001-12-04 | 2003-06-12 | Schering Corporation | N-aryl-n'-arylcycloalkyl-urea derivatives as mch antagonists for the treatment of obesity |
EP3452450A1 (en) * | 2016-05-04 | 2019-03-13 | Bristol-Myers Squibb Company | Inhibitors of indoleamine 2,3-dioxygenase and methods of their use |
CN110498769A (zh) * | 2018-05-17 | 2019-11-26 | 南京药捷安康生物科技有限公司 | Ido抑制剂与应用 |
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EP0344425B1 (en) * | 1988-03-30 | 1993-12-08 | Warner-Lambert Company | N-[[(2,6-disubstituted)phenyl]-N'- arylalkyl] ureas as antihypercholesterolemic and antiatherosclerotic agents |
US4868210A (en) * | 1988-03-30 | 1989-09-19 | Warner-Lambert Company | Antihyperlipidemic and antiatherosclerotic compounds and compositions |
CA2010184A1 (en) * | 1989-02-17 | 1990-08-17 | Bharat K. Trivedi | Antihyperlipidemic and antiatherosclerotic trisubstituted urea compounds |
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1992
- 1992-04-01 TW TW081102460A patent/TW209868B/zh active
- 1992-04-02 EP EP92105655A patent/EP0507291A1/en not_active Withdrawn
- 1992-04-03 CA CA002065086A patent/CA2065086A1/en not_active Abandoned
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CA2065086A1 (en) | 1992-10-05 |
EP0507291A1 (en) | 1992-10-07 |
HUT61724A (en) | 1993-03-01 |
HU9201138D0 (en) | 1992-06-29 |
TW209868B (ko) | 1993-07-21 |
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