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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67458생성일: 2026년 10월 24일

4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one → 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde

https://huagongshe.com/ko/reaction/67458

반응식

참여 물질

역할이름HCID투입량
반응물4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851602—
촉매HCID 178418406HCID 178418406—
용매DichloromethaneHCID 6344—
생성물5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehydeHCID 19833020—

반응 단계

A mixture of 12.2 g (50 mmol) of 4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one, 80.0 g of manganese dioxide and 500 ml of absolute methylene chloride is stirred at room temperature for 1 hour under an argon atmosphere and subsequently the manganese dioxide is filtered off under suction over Dicalit while rinsing with methylene chloride. The filtrate is evaporated to dryness in vacuo. After warming the residue in ca 150 ml of ethyl acetate, there is obtained 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde of melting point 205°-207° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346034
출처 데이터셋uspto-grants-1982_08
ORD IDord-635965d67bd04b5895e34c39622f3c15
출처 메모uspto-grants-1982_08