Water → tert-butyl ((2S)-1-((2-(4-propoxyphenyl)-1-benzofuran-6-yl)oxy)propan-2-yl)carbamate
反応式
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[O:12][C:13]3[CH:19]=[C:18]([OH:20])[CH:17]=[CH:16][C:14]=3[CH:15]=2)=[CH:7][CH:6]=1)[CH2:2][CH3:3].[H-].[Na+].CC1C=CC(S(O[CH2:34][C@@H:35]([NH:37][C:38]([O:40][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:39])[CH3:36])(=O)=O)=CC=1.O>CN(C=O)C>[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[O:12][C:13]3[CH:19]=[C:18]([O:20][CH2:36][C@@H:35]([NH:37][C:38](=[O:39])[O:40][C:41]([CH3:42])([CH3:44])[CH3:43])[CH3:34])[CH:17]=[CH:16][C:14]=3[CH:15]=2)=[CH:7][CH:6]=1)[CH2:2][CH3:3]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 2-(4-propoxyphenyl)-1-benzofuran-6-ol (918 mg) in DMF (10 mL) was added sodium hydride (60% oil, 137 mg), and the mixture was stirred at room temperature for 10 min. To the reaction mixture was added (2S)-2-[(tert-butoxycarbonyl)amino]propyl 4-methylbenzenesulfonate (1.13 g), and the mixture was stirred at 60° C. for 1 hr. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (460 mg).
後処理
- stirringthe mixture was stirred at 60° C. for 1 hr
- extractionthe mixture was extracted with ethyl acetate
- washThe obtained organic layer was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was evaporated under reduced pressure
- customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate)
出典と根拠
- ORDレコード
- ord-2738675bca0c4bd9990c4f5869be681f
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133129B2
反応ノート
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