Реакция #443383

Уравнение реакции

2,3,9,10a-Tetrahydrobenzo[b]cyclopenta[e][1,4]-diazepin-10(1H)-one

sodium hydrogencarbonate

sodium cyanoborohydride

hydrogen chloride methanol

→

titled compound

2,3,3a,4,9,10a-Hexahydrobenzo[b]cyclopenta-[e][1,4]diazepin-10(1H)-one

Растворители

methanol

tetrahydrofuran

water

Условия реакции

Обработка

1. 1
   Экстракцияfollowed by extraction with chloroform three times
2. 2
   Промывкаwashed with water
3. 3
   Сушкаa saturated aqueous solution of sodium chloride, dried over sodium sulfate
4. 4
   Фильтрацияsubjected to filtration
5. 5
   КонцентрированиеThe filtrate was concentrated under reduced pressure

Методика

2,3,9,10a-Tetrahydrobenzo[b]cyclopenta[e][1,4]-diazepin-10(1H)-one (38.3 g, 0.19 mmol) and bromocresol green (30 mg) were suspended in a mixture of methanol (200 mL) and tetrahydrofuran (200 mL), which was cooled to 0° C. To the suspension was added, at the same temperature, sodium cyanoborohydride (13.2 g, 0.21 mmol), to which was then added dropwise gradually a 10% hydrogen chloride-methanol solution until no more color change of the reaction system was observed. To the reaction mixture was added water (500 mL), which was made alkaline with a saturated aqueous solution of sodium hydrogencarbonate, followed by extraction with chloroform three times. Organic layers were combined, washed with water and a saturated aqueous solution of sodium chloride, dried over sodium sulfate and subjected to filtration. The filtrate was concentrated under reduced pressure to give 38.5 g (yield 99%) of the titled compound. The sample for analytical use was prepared by recrystallization from ethanol as a cis-trans mixture (1:1). m.p. 191°-212° C.

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