3-(Trifluoromethoxy)aniline → 6-Bromo-N-(3-(trifluoromethoxy)phenyl)imidazo[1,2-a]pyridine-2-carboxamide
反応式
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:5]=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7].[Br:13][C:14]1[CH:15]=[CH:16][C:17]2[N:18]([CH:20]=[C:21]([C:23](OCC)=[O:24])[N:22]=2)[CH:19]=1>>[Br:13][C:14]1[CH:15]=[CH:16][C:17]2[N:18]([CH:20]=[C:21]([C:23]([NH:7][C:6]3[CH:8]=[CH:9][CH:10]=[C:4]([O:3][C:2]([F:11])([F:12])[F:1])[CH:5]=3)=[O:24])[N:22]=2)[CH:19]=1参加物
3
実験手順
The title compound was prepared by essentially following the same procedures described for Intermediate I, using 3-(trifluoromethoxy)aniline and ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate as starting materials.
出典と根拠
- ORDレコード
- ord-f0519d74b8b44097a2d813d0a89f2df9
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09271969B2
反応ノート
読み込み中…