Water → tert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-(3-hydroxypropoxy)pyrrolidine-1-carboxylate
反応式
[Si]([O:8][CH2:9][CH2:10][CH2:11][O:12][C@H:13]1[CH2:17][N:16]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[C@H:15]([C:25]([N:27]([CH3:29])[CH3:28])=[O:26])[CH2:14]1)(C(C)(C)C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-].O>C1COCC1>[CH3:29][N:27]([CH3:28])[C:25]([C@@H:15]1[CH2:14][C@@H:13]([O:12][CH2:11][CH2:10][CH2:9][OH:8])[CH2:17][N:16]1[C:18]([O:20][C:21]([CH3:23])([CH3:22])[CH3:24])=[O:19])=[O:26]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 2.10 g of the compound obtained in Step 139-1 in THF (100 ml) was added a solution 1 mol/L TBAF in THF (10 ml) under ice cooling and the reaction mixture was stirred at room temperature for two hours. Water was poured, the solution was extracted twice with CHCl3; the combined organic layer was washed with saturated brine and dried over MgSO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N; mobile phase: CHCl3/MeOH=20/1 to 10/1; v/v) to obtain 1.79 g of the title compound.
後処理
- extractionthe solution was extracted twice with CHCl3
- washthe combined organic layer was washed with saturated brine
- dry with materialdried over MgSO4
- customthe drying agent was separated by filtration
- customthe solvent was evaporated under reduced pressure
- customThe obtained residue was purified by column chromatography (silicagel 60N; mobile phase: CHCl3/MeOH=20/1 to 10/1; v/v)
出典と根拠
- ORDレコード
- ord-4550fb3c03414ae7a5b0e59b97e9ef18
- 出典データセット
- uspto-grants-2011_10
- 特許番号
- US08030499B2
反応ノート
読み込み中…