Tetrabutylammonium Fluoride → methyl 1-allyl-3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1H-indole-6-carboxylate
反応式
[CH2:1]([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH3:16])=[O:14])[CH:11]=2)[C:6]([CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[C:5]1[C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[CH:25][C:24]=1[CH2:31][O:32][Si](C(C)C)(C(C)C)C(C)C)[CH:2]=[CH2:3].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[CH2:1]([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH3:16])=[O:14])[CH:11]=2)[C:6]([CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[C:5]1[C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[CH:25][C:24]=1[CH2:31][OH:32])[CH:2]=[CH2:3]参加物
4
実験手順
Methyl 1-allyl-3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1H-indole-6-carboxylate (1 eq) was dissolved in THF (0.28M solution) and a 1M solution of tetrabutylammonium fluoride in THF (1 eq) was added. The mixture was stirred at RT for 2 h, then all volatiles were evaporated in vacuo and the residual material was dissolved in Et2O. The solution was washed with 1N HCl, saturated aq. NaHCO3 solution and with brine. The organic phase was dried over Na2SO4 and evaporated in vacuo. The residual material was purified by FC (PE:EtOAc, 8:2). After evaporation of the solvents the product was obtained as colourless foam (88%). (ES+): m/z 434.2 (M+H)+.
後処理
- customall volatiles were evaporated in vacuo
- dissolutionthe residual material was dissolved in Et2O
- washThe solution was washed with 1N HCl, saturated aq. NaHCO3 solution and with brine
- dry with materialThe organic phase was dried over Na2SO4
- customevaporated in vacuo
- customThe residual material was purified by FC (PE:EtOAc, 8:2)
- customAfter evaporation of the solvents the product
出典と根拠
- ORDレコード
- ord-32d345ae3910424da8d23045ad11626e
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07989438B2
反応ノート
読み込み中…