Tetrabutylammonium Fluoride → Methyl 3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1-prop-2-yn-1-yl-1H-indole-6-carboxylate
반응식
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[CH:19]1([C:25]2[C:33]3[C:28](=[CH:29][C:30]([C:34]([O:36][CH3:37])=[O:35])=[CH:31][CH:32]=3)[N:27]([CH2:38][C:39]#[CH:40])[C:26]=2[C:41]2[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[CH:43][C:42]=2[CH2:49][O:50][Si](C(C)C)(C(C)C)C(C)C)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>C1COCC1.CCOC(C)=O>[CH:19]1([C:25]2[C:33]3[C:28](=[CH:29][C:30]([C:34]([O:36][CH3:37])=[O:35])=[CH:31][CH:32]=3)[N:27]([CH2:38][C:39]#[CH:40])[C:26]=2[C:41]2[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[CH:43][C:42]=2[CH2:49][OH:50])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1참가 물질
5
반응 조건
- 온도
- 0 °C
실험 절차
Tetrabutylammonium fluoride (1.3 eq., 1M solution in THF) was added dropwise to an ice cooled solution of methyl 3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1-prop-2-yn-1-yl-1H-indole-6-carboxylate in THF (0.036M). The mixture was stirred at 0° C. for 1 h then diluted with EtOAc, washed with saturated aq. NH4Cl, water and brine. The organic phase was dried over Na2SO4 and evaporated in vacuo. The residual material was subjected to flash chromatography (PE:EtOAc, 3:1). After evaporation of the solvent the product was obtained as white solid (64%). MS (ES+): 432.5 (M+H+).
후처리
- washwashed with saturated aq. NH4Cl, water and brine
- dry with materialThe organic phase was dried over Na2SO4
- customevaporated in vacuo
- customAfter evaporation of the solvent the product
출처 및 근거
- ORD 기록
- ord-113387404cd845a4a2130d12b5810501
- 출처 데이터셋
- uspto-grants-2012_07
- 특허 번호
- US08232390B2
반응 노트
불러오는 중…