反応式
[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]=1参加物
3
反応物 2
生成物 1
実験手順
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]+.
出典と根拠
- ORDレコード
- ord-1f330cca793645e39367c31670f98779
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08653127B2
関連ノート
読み込み中…