Phenacyl bromide → 2-(2-Hydroxyethylamino)-1-phenacylbenzimidazole dihydrobromide
反応式
[OH:1][CH2:2][CH2:3][NH:4][C:5]1[NH:6][C:7]2[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=2[N:9]=1.[CH2:14]([Br:23])[C:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:16]>CC(O)C>[BrH:23].[BrH:23].[OH:1][CH2:2][CH2:3][NH:4][C:5]1[N:6]([CH2:14][C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:16])[C:7]2[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=2[N:9]=1参加物
4
実験手順
Heat at reflux for three hours 8.95 g (50 mmol) of 2-(2-hydroxyethylamino)benzimidazole and 10 g of phenacyl bromide in 100 ml of 2-propanol. Allow to cool. Suction-filter the resulting precipitate and wash with acetone. The title compound is obtained.
後処理
- temperatureHeat
- temperatureto cool
- filtrationSuction-filter the resulting precipitate
- washwash with acetone
出典と根拠
- ORDレコード
- ord-6a76d4a93fea4c46b3f99c791933bc4f
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05623073
反応ノート
読み込み中…