Реакция #640531
ord-57cb82a95d384ee4b75e6f8e4bb38f56
Уравнение реакции
4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
→
title compound
4-[1-(3-Amino-4-chlorophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
Реагенты
Условия реакции
Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ФильтрацияFiltration and evaporation at reduced pressure
- 2Другоеgives the crude product
- 3ДругоеPurification
- 4Экстракцияby extraction with ethyl acetate and chromatography on silicagel
Методика
To a stirred solution of 4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine (0.07 g, 0.175 mmol) in ethanol (6 ml) and water (1 ml) is added two drops of concentrated hydrochloric acid and iron powder (0.1 g, 17.5 mmol). The reaction mixture is heated at 80° C. for 8 hours. Filtration and evaporation at reduced pressure gives the crude product. Purification by extraction with ethyl acetate and chromatography on silicagel yields the title compound as colorless solid, m.p. 228-230° C.