5-(4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione → 5-(-[4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]phenyl]methyl)thiazolidine-2,4-dione
반응식
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][O:17][C:18]2[CH:31]=[CH:30][C:21]([CH:22]=[C:23]3[S:27][C:26](=[O:28])[NH:25][C:24]3=[O:29])=[CH:20][CH:19]=2)=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H][H]>C(OCC)(=O)C.[Pd]>[C:1]([O:5][C:6]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][O:17][C:18]2[CH:31]=[CH:30][C:21]([CH2:22][CH:23]3[S:27][C:26](=[O:28])[NH:25][C:24]3=[O:29])=[CH:20][CH:19]=2)=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
A solution of 0.5 g (1.14 mmole) 5-(4-[2-(4-tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione in ethyl acetate was hydrogenated in the presence of 5% palladium on charcoal at room temperature and atmospheric pressure until hydrogen uptake ceased. The solution was filtered through celite, the filter pad was washed with ethyl acetate and the filtrate was evaporated to give 0.5 g (yield 99%) of 5-(-[4-[2-(4-tert-butyloxycarbonylaminophenyl)ethoxy]phenyl]methyl)thiazolidine-2,4-dione.
후처리
- filtrationThe solution was filtered through celite
- washthe filter pad was washed with ethyl acetate
- customthe filtrate was evaporated
출처 및 근거
- ORD 기록
- ord-d62f5c846e2a404ebb9acfc1910157cc
- 출처 데이터셋
- uspto-grants-2001_09
- 특허 번호
- US06288096B1
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