Acetyl chloride → 2-Methyl-2-(2-pyridyl)-1H-benzimidazole
反応式
CO[C:3]1[CH:15]=[CH:14][C:6]([NH:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10]N=2)=[C:5]([NH2:16])[CH:4]=1.[C:17](Cl)(=O)C.[N:21]1C=CC=C[C:22]=1N1C2C=CC=CC=2N=C1/C=C/C1C=CC=CC=1>>[CH3:17][C:8]1([C:13]2[CH:12]=[CH:11][CH:10]=[CH:22][N:21]=2)[NH:7][C:6]2[CH:14]=[CH:15][CH:3]=[CH:4][C:5]=2[NH:16]1参加物
4
実験手順
The titled compound was prepared from 4-methoxy-2-amino-N-(2-pyridyl)aniline and acetyl chloride according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A).
出典と根拠
- ORDレコード
- ord-9c78612176904a94bf27399d98c02448
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06713482B2
反応ノート
読み込み中…