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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67320생성일: 2026년 10월 24일

Potassium Cyanide → methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/ko/reaction/67320

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CyanideHCID 9032—
반응물Ro 14-7437HCID 127597—
용매MethanolHCID 887—
생성물methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylateHCID 10378479—

반응 단계

285 mg (1 mmol) of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate and 66 mg of potassium cyanide are heated to boiling under reflux for 24 hours in 10 ml of methanol. Then, the mixture is concentrated on a rotary evaporator, the residue is partitioned between water and chloroform, extracted twice with chloroform, the chloroform phase is dried over magnesium sulphate and evaporated. There is obtained methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 212°-214° C. This product is uniform according to thin-layer chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346030
출처 데이터셋uspto-grants-1982_08
ORD IDord-2343817238154b91a71b7b1a643bedcf
출처 메모uspto-grants-1982_08