KR100848429B1 - 치환된 알킬아민 유도체 및 그의 사용 방법 - Google Patents
치환된 알킬아민 유도체 및 그의 사용 방법 Download PDFInfo
- Publication number
- KR100848429B1 KR100848429B1 KR1020037009274A KR20037009274A KR100848429B1 KR 100848429 B1 KR100848429 B1 KR 100848429B1 KR 1020037009274 A KR1020037009274 A KR 1020037009274A KR 20037009274 A KR20037009274 A KR 20037009274A KR 100848429 B1 KR100848429 B1 KR 100848429B1
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- KR
- South Korea
- Prior art keywords
- amino
- substituted
- ylmethyl
- boc
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 CCCCC(C)(CCCCN(C)NC*)N=C=C Chemical compound CCCCC(C)(CCCCN(C)NC*)N=C=C 0.000 description 9
- CUJNZTKYZLLKBY-UHFFFAOYSA-N CC(C)(C)c1n[nH]c(C)c1 Chemical compound CC(C)(C)c1n[nH]c(C)c1 CUJNZTKYZLLKBY-UHFFFAOYSA-N 0.000 description 1
- PTVCFDQSJWNKIJ-UHFFFAOYSA-N CC(C)(CN(C(C)=O)c1c2)c1ccc2NC(c1c(NCC2CCOCC2)nccc1)=O Chemical compound CC(C)(CN(C(C)=O)c1c2)c1ccc2NC(c1c(NCC2CCOCC2)nccc1)=O PTVCFDQSJWNKIJ-UHFFFAOYSA-N 0.000 description 1
- DHVHQZSWWJWAHU-UHFFFAOYSA-N CC(C)c(cc1)ccc1NC(c(cc1)c(NCc2ccncc2)nc1F)=O Chemical compound CC(C)c(cc1)ccc1NC(c(cc1)c(NCc2ccncc2)nc1F)=O DHVHQZSWWJWAHU-UHFFFAOYSA-N 0.000 description 1
- FUBGESDOASSFLE-UHFFFAOYSA-N Cc(cc1)nc(NCc2ccncc2)c1C(Nc(cc1)cc(Cl)c1Cl)=O Chemical compound Cc(cc1)nc(NCc2ccncc2)c1C(Nc(cc1)cc(Cl)c1Cl)=O FUBGESDOASSFLE-UHFFFAOYSA-N 0.000 description 1
- LUYISICIYVKBTA-UHFFFAOYSA-N Cc1cc2cccnc2cc1 Chemical compound Cc1cc2cccnc2cc1 LUYISICIYVKBTA-UHFFFAOYSA-N 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N Cc1cccnc1C Chemical compound Cc1cccnc1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- NURQLCJSMXZBPC-UHFFFAOYSA-N Cc1ccncc1C Chemical compound Cc1ccncc1C NURQLCJSMXZBPC-UHFFFAOYSA-N 0.000 description 1
- DJBWOZWLNICJDD-UHFFFAOYSA-N O=C(c(cc1)c(NCc2ccncc2)nc1Cl)Nc(cc1)ccc1Cl Chemical compound O=C(c(cc1)c(NCc2ccncc2)nc1Cl)Nc(cc1)ccc1Cl DJBWOZWLNICJDD-UHFFFAOYSA-N 0.000 description 1
- VZOQOTFQDURGAQ-UHFFFAOYSA-N O=C(c(cc1)c(NCc2ccncc2)nc1Cl)Nc1cc(F)ccc1 Chemical compound O=C(c(cc1)c(NCc2ccncc2)nc1Cl)Nc1cc(F)ccc1 VZOQOTFQDURGAQ-UHFFFAOYSA-N 0.000 description 1
- DVIUDAIRNHXRFA-UHFFFAOYSA-N O=C(c(cc1)c(NCc2ccncc2)nc1F)Nc1cccc(C(F)(F)F)c1 Chemical compound O=C(c(cc1)c(NCc2ccncc2)nc1F)Nc1cccc(C(F)(F)F)c1 DVIUDAIRNHXRFA-UHFFFAOYSA-N 0.000 description 1
- DTGXNZDPFAXKMU-UHFFFAOYSA-N O=C(c1c(NCc2ccncc2)nccc1)Nc1cccc(C(F)(F)F)c1 Chemical compound O=C(c1c(NCc2ccncc2)nccc1)Nc1cccc(C(F)(F)F)c1 DTGXNZDPFAXKMU-UHFFFAOYSA-N 0.000 description 1
- RLCSOSKPEXBPHZ-UHFFFAOYSA-N O=C(c1cccnc1NCc1ccncc1)Nc(cc1)ccc1-[n]1cncc1 Chemical compound O=C(c1cccnc1NCc1ccncc1)Nc(cc1)ccc1-[n]1cncc1 RLCSOSKPEXBPHZ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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| AP2004003100A0 (en) | 2002-02-11 | 2004-09-30 | Pfizer | Nicotinamide derivatives useful as PDE4 inhibitors |
| US20030195192A1 (en) | 2002-04-05 | 2003-10-16 | Fortuna Haviv | Nicotinamides having antiangiogenic activity |
| US7517894B2 (en) | 2002-07-31 | 2009-04-14 | Bayer Schering Pharma Ag | VEGFR-2 and VEGFR-3 inhibitory anthranilamide pyridines |
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| WO2000027280A1 (en) * | 1998-11-06 | 2000-05-18 | London Health Sciences Centre | A multi-channel data acquisition system for the real-time spatial, temporal monitoring and classification of high frequency bandwidth neuronal activity |
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