반응식
[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][N:6]2S(C1C=CC(C)=CC=1)(=O)=O.[CH3:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][C:24]=1[S:30](Cl)(=[O:32])=[O:31]>>[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][N:6]2[S:30]([C:24]1[CH:25]=[C:26]([CH3:29])[CH:27]=[CH:28][C:23]=1[O:22][CH3:21])(=[O:32])=[O:31]참가 물질
3
실험 절차
The procedure for Intermediate 3 was followed using (2-methoxy-5-methylphenyl)sulfonyl chloride. Yield 1.4 g (72%). MS (ESI+) for C16H14BrNO3S m/z 382 (M+H)+.
출처 및 근거
- ORD 기록
- ord-b5096f3a8d1e4e658724f6b636ebf32a
- 출처 데이터셋
- uspto-grants-2010_10
- 특허 번호
- US07812017B2
연결된 노트
불러오는 중…