반응식
[OH-].[Na+].[F:3][C:4]1[CH:5]=[CH:6][C:7]([C:28]2[C:33]([CH3:34])=[CH:32][C:31]([CH2:35][CH2:36][C:37]([OH:40])([CH3:39])[CH3:38])=[CH:30][C:29]=2[CH3:41])=[C:8]2[C:12]=1[C@H:11]([O:13][C:14]1[CH:27]=[CH:26][C:17]3[C@H:18]([CH2:21][C:22]([O:24]C)=[O:23])[CH2:19][O:20][C:16]=3[CH:15]=1)[CH2:10][CH2:9]2>CO>[F:3][C:4]1[CH:5]=[CH:6][C:7]([C:28]2[C:33]([CH3:34])=[CH:32][C:31]([CH2:35][CH2:36][C:37]([OH:40])([CH3:38])[CH3:39])=[CH:30][C:29]=2[CH3:41])=[C:8]2[C:12]=1[C@H:11]([O:13][C:14]1[CH:27]=[CH:26][C:17]3[C@H:18]([CH2:21][C:22]([OH:24])=[O:23])[CH2:19][O:20][C:16]=3[CH:15]=1)[CH2:10][CH2:9]2참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 50 °C
실험 절차
1 M aqueous NaOH solution (310 μL) is added to a solution of methyl 2-((S)-6-((R)-7-fluoro-4-(4-(3-hydroxy-3-methylbutyl)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate (110 mg) in methanol (4 mL). The mixture is stirred at room temperature for 12 hours and at 50° C. for 2 days. 1 M aqueous NaOH solution (100 μL) is added and the mixture is stirred at 50° C. for 1 hour. Methanol is evaporated in vacuo, the residue is diluted with water and neutralized with 1 M aqueous HCl. The resulting mixture is extracted with ethyl acetate, and the combined organic phases are washed with brine and dried (MgSO4). The solvent is evaporated to give the title compound. Yield: 80 mg; LC (method 8): tR=0.59 min; Mass spectrum (ESI+): m/z=519 [M+H]+.
후처리
- stirringthe mixture is stirred at 50° C. for 1 hour
- customMethanol is evaporated in vacuo
- additionthe residue is diluted with water and neutralized with 1 M aqueous HCl
- extractionThe resulting mixture is extracted with ethyl acetate
- washthe combined organic phases are washed with brine
- dry with materialdried (MgSO4)
- customThe solvent is evaporated
출처 및 근거
- ORD 기록
- ord-efbe6109626048c3a398ab640781c4f8
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642585B2
연결된 노트
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