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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606954생성일: 2026년 10월 25일

Water → 7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1606954

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepine--oneHCID 86743356—
용매DimethylformamideHCID 6228—
생성물7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851533—

반응 단계

20.2 g (65.5 mmol) of 7-chloro-3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepine--one was heated to boiling under reflux for 5 hours together with 11.7 ml (78.5 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene in 200 ml of N,N-dimethylformamide. The reaction mixture was subsequently poured into 800 ml of water and extracted four time with methylene chloride. The organic extracts were washed four times with water, dried over magnesium sulphate and evaporated. After chromatography of the residue on silica gel while eluting with ethyl acetate and two successive crystallizations from acetonitrile and from ethyl acetate there was obtained 7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 201°-202°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04863920
출처 데이터셋uspto-grants-1989_09
ORD IDord-cbbe1afd9e4849a7a994b5b2448f4990
출처 메모uspto-grants-1989_09