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HRID 356201作成日:2026年10月24日

Sodium Bicarbonate → 2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

https://huagongshe.com/ja/reaction/356201

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2,3,9,10a-Tetrahydro-1H-benzo[b]cyclopenta[f][1,4]diazepin-10-oneHCID 12394935—
反応物Hydrochloride methanolHCID 21893726—
触媒Bromocresol GreenHCID 6451—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 18940590100,187.5%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834463
出典データセットuspto-grants-1998_11
ORD IDord-0a8b08a493824814808e84cd6b43072d
出典メモuspto-grants-1998_11