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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606953생성일: 2026년 10월 26일

Sodium amide → 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1606953

반응식

참여 물질

역할이름HCID투입량
반응물Sodium amideHCID 24533—
반응물(Chloromethyl)triphenylphosphonium chlorideHCID 197823—
반응물7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehydeHCID 19851584—
용매TetrahydrofuranHCID 8028—
생성물7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 86743355—

반응 단계

100 g of an equimolar mixture of chloromethyltriphenylphosphonium chloride and sodium amide were stirred for 45 minutes in 450 ml of tetrahydrofuran, whereby the temperature rose to 37°. 62.23 g (229.7 mmol) of 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde were then added portionwise thereto at room temperature and, after completion of the addition, the mixture was stirred for a further 1 hour. The reaction mixture was subsequently filtered and the filtrate was evaporated. After chromatography of the residue on silica gel while eluting with cyclohexane/ether/wasopropanol (3:3:1) there was obtained 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 205°-207°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04863920
출처 데이터셋uspto-grants-1989_09
ORD IDord-4e6d176c92604bb192e57a7ddecd8b8f
출처 메모uspto-grants-1989_09