Sodium hydride → 4-{[(1R,3S,4S)-3-([tert-butyl(dimethyl)silyl]oxy}-4-({[tert-butyl(dimethyl)silyl]oxy)methyl)cyclopentyl]oxy}-3-nitropyridin-2-amine
반응식
[Si:1]([O:8][CH2:9][CH:10]1[CH2:14][CH:13]([OH:15])[CH2:12][CH2:11]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[H-].[Na+].[NH2:18][C:19]1[C:24]([N+:25]([O-:27])=[O:26])=[C:23](Cl)[CH:22]=[CH:21][N:20]=1>C1COCC1>[Si:1]([O:8][C@@H:11]1[C@H:10]([CH2:9][O:8][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])[CH2:14][C@@H:13]([O:15][C:23]2[CH:22]=[CH:21][N:20]=[C:19]([NH2:18])[C:24]=2[N+:25]([O-:27])=[O:26])[CH2:12]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of (1R,3S,4S)-3-f[tert-butyl(dimethyl)silyl]oxy}-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanol (0.782 g, 0.00217 mol) in THF (30.0 mL) was added NaH (0.156 g, 0.00650 mol) and the mixture was stirred for 1 h. To this was added 2-amino-4-chloro-3-nitropyridine (0.376 g, 0.00217 mol) and the mixture was stirred overnight. The solution was concentrated and the residue was purified by flash chromatography (25% EtOAc/hexanes) to afford the title compound (0.381 g, 35%) as a yellow solid.
후처리
- stirringthe mixture was stirred overnight
- concentrationThe solution was concentrated
- customthe residue was purified by flash chromatography (25% EtOAc/hexanes)
출처 및 근거
- ORD 기록
- ord-bd01f0f83d13403c83f67fede5a2ed1d
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08901136B2
반응 노트
불러오는 중…