반응식
[CH3:1][C:2]([CH3:30])([CH3:29])[C@H:3]([NH:7][C:8]([N:10]1[C:18]2[CH2:17][CH2:16][N:15]([CH3:19])[CH2:14][C:13]=2[C:12]([C:20]2[CH:25]=[C:24]([F:26])[C:23](F)=[CH:22][C:21]=2[F:28])=[N:11]1)=[O:9])[C:4]([OH:6])=[O:5].FC1C=CC(F)=CC=1C(Cl)=O>>[F:28][C:21]1[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:20]=1[C:12]1[C:13]2[CH2:14][N:15]([CH3:19])[CH2:16][CH2:17][C:18]=2[N:10]([C:8]([NH:7][C@@H:3]([C:2]([CH3:30])([CH3:29])[CH3:1])[C:4]([OH:6])=[O:5])=[O:9])[N:11]=1참가 물질
3
반응물 2
생성물 1
실험 절차
Compound 81 was prepared according to the procedure described for the synthesis of compound 71 by replacing 2,4,5-trifluorobenzoyl chloride with 2,5-difluoro-benzoyl chloride in the synthesis of intermediate 19. LCMS (+ESI) m/z=407.2 [M+H]+.
출처 및 근거
- ORD 기록
- ord-1f330cca793645e39367c31670f98779
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08653127B2
연결된 노트
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