反应详情

130 Milligrams of lithium aluminum hydride was suspended in 70 ml of tetrahydrofuran, then 2.2 g of 6-amino-3,4-dihydro-2(1H)-quinolinone was added gradually thereto, and the mixture was stirred at room temperature overnight. The reaction mixture was further stirred for 2 hours under refluxing condition, then 1 g of methyl 1-benzyl-6-chlorobenzimidazol-2-carboxylate was added, the reaction was continued by refluxing for 3 hours. After the reaction was finished, then water and 10% aqueous solution of potassium hydroxide were added, the reaction mixture was diluted with ethyl acetate and filtered with Celite, and the filtrate was washed with chloroform, the solvent was removed by distillation under reduced pressure. To the residue thus obtained was added ethanol and heated, the insoluble matters were collected by filtration and recrystallized from dimethylformamide, there was obtained 0.11 g of 1-benzyl-6-chloro-2-(3,4-dihydro-2(1H)-quinolinon-6-ylaminocarbonyl)benzimidazole as in the form of yellow powdery product.

1. stirringThe reaction mixture was further stirred for 2 hours
2. temperatureunder refluxing condition
3. temperatureby refluxing for 3 hours
4. filtrationfiltered with Celite
5. washthe filtrate was washed with chloroform
6. customthe solvent was removed by distillation under reduced pressure
7. customTo the residue thus obtained
8. temperatureheated
9. filtrationthe insoluble matters were collected by filtration
10. customrecrystallized from dimethylformamide