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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356195생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/356195

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물GlutarimideHCID 70726—
반응물(3aR*,10aS*)-9-benzyl-4-(bromoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]-cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 70109710—
용매DimethylformamideHCID 6228—
생성물Benzyl-4-(glutarimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]-diazepin-10(1H)-oneHCID 86753323114.1%

반응 단계

To a solution of glutarimide (136 mg, 1.2 mmol) in N,N-dimethylformamide (2 mL) was added, at 0° C., sodium hydride (60% liquid paraffin dispersion, 44 mg, 1.1 mmol), and the mixture was stirred for 5 minutes. To this mixture was added (3aR*,10aS*)-9-benzyl-4-(bromoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]-cyclopenta[e][1,4]diazepin-10(1H)-one (413 mg, 1 mmol), and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride (4 mL), which was subjected to extraction twice with chloroform. Organic layers were combined, washed with water and dried over magnesium sulfate, which was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was crystallized from ethyl acetate-diethyl ether to give 305 mg (yield 68%) of the titled compound, m.p. 220°-221° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834463
출처 데이터셋uspto-grants-1998_11
ORD IDord-bfa728810a9f4ffea5191033a67ef55a
출처 메모uspto-grants-1998_11