Water → 1,1-Dimethylethyl [(4r)-4-(5-chloro-2-cyano-4-fluorophenoxy)-4-(1-methyl-1h-imidazol-2-yl)butyl]-carbamate
반응식
[CH3:1][C:2]([O:5][C:6](=[O:19])[NH:7][CH2:8][CH2:9][CH2:10][C@@H:11]([OH:18])[C:12]1[N:13]([CH3:17])[CH:14]=[CH:15][N:16]=1)([CH3:4])[CH3:3].[H-].[Na+].[Cl:22][C:23]1[C:30]([F:31])=[CH:29][C:26]([C:27]#[N:28])=[C:25](F)[CH:24]=1.O>CN(C)C=O>[Cl:22][C:23]1[C:30]([F:31])=[CH:29][C:26]([C:27]#[N:28])=[C:25]([CH:24]=1)[O:18][C@@H:11]([C:12]1[N:13]([CH3:17])[CH:14]=[CH:15][N:16]=1)[CH2:10][CH2:9][CH2:8][NH:7][C:6](=[O:19])[O:5][C:2]([CH3:1])([CH3:3])[CH3:4]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
The product of step (b) (0.24 g, 0.9 mmol) was dissolved in dry dimethylformamide (20 ml), sodium hydride (60% dispersion in oil, 0.04 g, 0.95 mmol) was added in one portion and the mixture stirred at room temperature for 0.5 h. 4-Chloro-2,5-difluorobenzonitrile (0.16 g, 0.9 mmol), as a solution in dry dimethylformamide (5 ml), was added dropwise and the reaction stirred for 18hat room temperature. Water (25 ml) was added and the reaction mixture extracted with ethyl acetate (3×60 ml). The combined organic extracts were washed with water (2×20 ml), dried (magnesium sulphate) and evaporated. The residue was eluted down a flash chromatography column using hexane:ethyl acetate (1:3) as eluent to give the sub-title compound as a white crystalline solid (0.34 g, 88%).
후처리
- stirringthe reaction stirred for 18hat room temperature
- extractionthe reaction mixture extracted with ethyl acetate (3×60 ml)
- washThe combined organic extracts were washed with water (2×20 ml)
- dry with materialdried (magnesium sulphate)
- customevaporated
- washThe residue was eluted down a flash chromatography column
출처 및 근거
- ORD 기록
- ord-45c373d6c6844181bfd1b0354ab65a95
- 출처 데이터셋
- uspto-grants-2004_06
- 특허 번호
- US06743939B2
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