Реакция #90159

Уравнение реакции

9-Ethyl-6,6-dimethyl-11-oxo-8-(4-oxopiperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

hydroxylamine hydrochloric acid salt

→

title compound

Выход 75.6%

9-Ethyl-8-(4-hydroxyimino-piperidin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

Выход 75.6%

Растворители

ethyl acetate

ethanol

Условия реакции

Обработка

1. 1
   ПромывкаThe organic layer was washed with 10% brine
2. 2
   Концентрированиеconcentrated under reduced pressure
3. 3
   ДругоеThe resulting residues were purified by silica gel column (dichloromethane/methanol=99/1 to 90/10)

Методика

9-Ethyl-6,6-dimethyl-11-oxo-8-(4-oxopiperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (30 mg) and hydroxylamine hydrochloric acid salt (10 mg) were dissolved in ethanol (5 ml) and stirred at 60° C. for 6 hrs. The reaction mixture was diluted with ethyl acetate (20 ml). The organic layer was washed with 10% brine and concentrated under reduced pressure. The resulting residues were purified by silica gel column (dichloromethane/methanol=99/1 to 90/10) to obtain the title compound (23.5 mg, yield 74%).

Источник