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[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])[CH2:5][NH2:6].[Cl:14][C:15]1[S:19][C:18]([NH:20][S:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28](O)=[O:29])=[C:26]([C:33]#[N:34])[CH:25]=2)(=[O:23])=[O:22])=[N:17][CH:16]=1>>[Cl:14][C:15]1[S:19][C:18]([NH:20][S:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28]([NH:6][CH2:5][C:4]3[CH:7]=[CH:8][C:9]([C:10]([F:11])([F:12])[F:13])=[C:2]([F:1])[CH:3]=3)=[O:29])=[C:26]([C:33]#[N:34])[CH:25]=2)(=[O:23])=[O:22])=[N:17][CH:16]=1참가 물질
3
실험 절차
The title compound was prepared from 3-fluoro-4-(trifluoromethyl)benzylamine and 4-{[(5-chloro-1,3-thiazol-2-yl)amino]sulfonyl}-2-cyanobenzoic acid of Preparation 22, following Method O described for Example 344. The reaction mixture was stirred at room temperature for 18 hours.
출처 및 근거
- ORD 기록
- ord-0421cfd3fdb94f7581d5516e348cb354
- 출처 데이터셋
- uspto-grants-2013_01
- 특허 번호
- US08357711B2
연결된 노트
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