반응식
[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]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
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.
후처리
- 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)
출처 및 근거
- ORD 기록
- ord-4550fb3c03414ae7a5b0e59b97e9ef18
- 출처 데이터셋
- uspto-grants-2011_10
- 특허 번호
- US08030499B2
연결된 노트
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