反応式
[C:1]([C:3]1[CH:4]=[C:5]([NH:9][C:10](=[O:12])[CH3:11])[CH:6]=[CH:7][CH:8]=1)#[CH:2].[CH2:13]([O:15][C:16]([C:18]1[N:19]([CH3:25])[C:20](Br)=[N:21][C:22]=1[CH3:23])=[O:17])[CH3:14]>>[CH2:13]([O:15][C:16]([C:18]1[N:19]([CH3:25])[C:20]([C:2]#[C:1][C:3]2[CH:8]=[CH:7][CH:6]=[C:5]([NH:9][C:10](=[O:12])[CH3:11])[CH:4]=2)=[N:21][C:22]=1[CH3:23])=[O:17])[CH3:14]参加物
3
実験手順
The title compound, MS: m/e=326.8 (M+H+), was prepared in accordance with the general method of example 1b from N-(3-ethynyl-phenyl)-acetamide and 2-bromo-3,5-dimethyl-3H-imidazole-4-carboxylic acid ethyl ester.
出典と根拠
- ORDレコード
- ord-5d7fdcec14f54bf692b945ee61aee2e2
- 出典データセット
- uspto-grants-2005_12
- 特許番号
- US06972299B2
関連ノート
読み込み中…