반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([NH2:20])[CH:11]=[N:12][C:13]=2[O:14][CH2:15][C:16]([F:19])([F:18])[F:17])=[CH:4][CH:3]=1.[S:21]1[CH:25]=[CH:24][N:23]=[C:22]1[C:26](O)=[O:27]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[C:10]([NH:20][C:26]([C:22]3[S:21][CH:25]=[CH:24][N:23]=3)=[O:27])[CH:11]=[N:12][C:13]=2[O:14][CH2:15][C:16]([F:17])([F:18])[F:19])=[CH:6][CH:7]=1참가 물질
3
실험 절차
The title compound was synthesized in analogy to Example 1, using 5-(4-chloro-phenyl)-6-(2,2, 2-trifluoro-ethoxy)-pyridin-3-ylamine and 2-thiazolecarboxylic acid as starting materials, MS (LC/MS): 414.0 (M+H).
출처 및 근거
- ORD 기록
- ord-1a2aca18d076416c8877ebd66194f311
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08410107B2
연결된 노트
불러오는 중…