HCID 178471895, 화합물 → ethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoate
반응식
[CH:1]1([NH:4][CH:5]=[C:6]([C:12](=[O:29])[C:13]2[C:18]([N+:19]([O-])=O)=[C:17]([F:22])[C:16]([F:23])=[C:15]([O:24][CH:25]([F:27])[F:26])[C:14]=2[F:28])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1>C(O)C>[CH:1]1([NH:4][CH:5]=[C:6]([C:12](=[O:29])[C:13]2[C:18]([NH2:19])=[C:17]([F:22])[C:16]([F:23])=[C:15]([O:24][CH:25]([F:26])[F:27])[C:14]=2[F:28])[C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1참가 물질
실험 절차
33.63 g (0.079 mole) of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate [(XIXa): X=X'=F, R1 =OCHF2, R17 =C2H5 ] were dissolved in 1300 ml of ethanol with heating. A stream of hydrogen was then bubbled through the solution in the presence of 8.4 g of 5% w/w palladium-on-carbon at room temperature for 40 minutes, whilst stirring. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The resulting residue was then purified by silica gel column chromatography using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 25.1 g of ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIXb): X=X'=F, R1 =OCHF2, R17 =C2H5 ] as a pale yellow powder, melting at 103°-104° C.
후처리
- temperaturewith heating
- customA stream of hydrogen was then bubbled through the solution in the presence of 8.4 g of 5% w/w palladium-on-carbon at room temperature for 40 minutes
- filtrationAt the end of this time, the reaction mixture was filtered
- concentrationthe filtrate was concentrated by evaporation under reduced pressure
- customThe resulting residue was then purified by silica gel column chromatography
- additionby volume mixture of toluene and ethyl acetate as the eluent
출처 및 근거
- ORD 기록
- ord-cde91cd436284f6eb7edf689d4d4bd9e
- 출처 데이터셋
- uspto-grants-1991_12
- 특허 번호
- US05073556
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