Aniline → [5-Fluoro-2-methyl-3-(2-phenylsulfamoylbenzyl)indol-1-yl]acetic acid methyl ester
반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[CH3:15][O:16][C:17](=[O:41])[CH2:18][N:19]1[C:27]2[C:22](=[CH:23][C:24]([F:28])=[CH:25][CH:26]=2)[C:21]([CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=2[S:36](Cl)(=[O:38])=[O:37])=[C:20]1[CH3:40]>ClCCl>[CH3:15][O:16][C:17](=[O:41])[CH2:18][N:19]1[C:27]2[C:22](=[CH:23][C:24]([F:28])=[CH:25][CH:26]=2)[C:21]([CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=2[S:36](=[O:38])(=[O:37])[NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:20]1[CH3:40]참가 물질
5
실험 절차
A mixture of aniline (0.022 mL), triethylamine (0.051 mL) and dichloromethane (0.5 mL) was treated with [3-(2-chlorosulfonylbenzyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester (0.10 g), and resulting mixture was stirred at room temperature for 4 days. The mixture was diluted with dichloromethane, washed with water and concentrated under reduced pressure to afford the title compound as a colourless gum (0.078 g).
후처리
- customresulting mixture
- washwashed with water
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-8dc7d95e33364601a613861b52f5e7a1
- 출처 데이터셋
- uspto-grants-2013_03
- 특허 번호
- US08394836B2
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