反応式
Cl[C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1.[NH:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1>C(O)C>[N:11]1([C:2]2[NH:6][C:5]3[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=3[N:3]=2)[CH2:15][CH2:14][CH2:13][CH2:12]1参加物
4
反応条件
- 温度
- 165 °C
実験手順
2-Chloro-1H-benzimidazole (10.0 g, 0.066 mol), pyrrolidine (18.5 g, 0.26 mol), and ethanol (100 mL) were combined. The resulting solution was heated at 160-170° C. for 6 hours and then the solvent was evaporated. The resulting residue was mixed with water. The mixture was made strongly acidic with hydrochloric acid and then made basic with ammonium hydroxide. The resulting solid was isolated by filtration, washed with water and then air dried to provide 11.8 g of crude product as a tan powder. This material was recrystallized from ethyl acetate/methanol to provide 4.9 g of 2-pyrrolidino-1H-benzimidazole.
後処理
- customthe solvent was evaporated
- additionThe resulting residue was mixed with water
- customThe resulting solid was isolated by filtration
- washwashed with water
- customair dried
- customto provide 11.8 g of crude product as a tan powder
- customThis material was recrystallized from ethyl acetate/methanol
出典と根拠
- ORDレコード
- ord-980e01e96f4642daa159b97b379cfc6c
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07393859B2
関連ノート
読み込み中…