Imidazole → 4-(1H-Imidazol-1-yl)-3-(trifluoromethyl)-benzonitrile
反応式
Cl[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[C:10]([F:13])([F:12])[F:11].[NH:14]1[CH:18]=[CH:17][N:16]=[CH:15]1>>[N:14]1([C:2]2[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=2[C:10]([F:13])([F:12])[F:11])[CH:18]=[CH:17][N:16]=[CH:15]1参加物
3
実験手順
The title compound is prepared using an analogous method as described in Example 1.1, utilising 4-chloro-3-(trifluoromethyl)-benzonitrile (Lancaster Synthesis, GmbH) and imidazole (Fluka, Buchs, Switzerland), with a reaction temperature of 110° C.
出典と根拠
- ORDレコード
- ord-8a144d5b61524a3d8d490a715cf2dd9e
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07655669B2
反応ノート
読み込み中…