反応式
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.[Br:12][C:13]1[CH:14]=[CH:15][C:16]2[N:17]([CH:19]=[C:20]([C:22](OCC)=[O:23])[N:21]=2)[CH:18]=1>>[Br:12][C:13]1[CH:14]=[CH:15][C:16]2[N:17]([CH:19]=[C:20]([C:22]([NH:7][C:6]3[CH:8]=[CH:9][C:3]([C:2]([F:10])([F:11])[F:1])=[CH:4][CH:5]=3)=[O:23])[N:21]=2)[CH:18]=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 4-(trifluoromethyl)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-d30046cef179424984895a7f1afb7cdb
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09271969B2
関連ノート
読み込み中…