反応式
F[C:2]1[CH:3]=[C:4]([N:8]2[CH:12]=[C:11]([C:13]#[C:14][C:15]3[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=3)[C:18]#[N:19])[N:10]=[C:9]2[CH3:23])[CH:5]=[N:6][CH:7]=1.Cl.[CH3:25][NH:26][CH3:27]>>[CH3:25][N:26]([CH3:27])[C:2]1[CH:3]=[C:4]([N:8]2[CH:12]=[C:11]([C:13]#[C:14][C:15]3[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=3)[C:18]#[N:19])[N:10]=[C:9]2[CH3:23])[CH:5]=[N:6][CH:7]=1参加物
3
実験手順
The title compound, MS: m/e=328.4 (M+), was prepared in accordance with the general method of example 27 from 3-[1-(5-fluoro-pyridin-3-yl)-2-methyl-1H-imidazol-4-ylethynyl]-benzonitrile and dimethylamine hydrochloride.
出典と根拠
- ORDレコード
- ord-b2ed5ff836664658b102f6cb0d37ccfe
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07241760B2
関連ノート
読み込み中…