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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414906생성일: 2026년 10월 25일

alpha-Hydroxyalprazolam → 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde

https://huagongshe.com/reaction/1414906

반응식

참여 물질

역할이름HCID투입량
반응물alpha-HydroxyalprazolamHCID 162244—
촉매HCID 178418406HCID 178418406—
용매BenzeneHCID 241—
생성물6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehydeHCID 21486011—

반응 단계

A mixture of 1.3 g of 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-methanol [cp., e.g. German `Offenlegungsschrift` No. 2,156,472, Belgian Pat. No. 775,558] , 3.4 g of manganese dioxide and 80 ml of benzene is refluxed for 2 hours. The reaction mixture is then filtered through a layer of silica gel, and the filtrate concentrated by evaporation. The residue is chromatographed through silica gel (Merck, 0.063 - 0.2 mm particle size) with various ethyl acetate/ethanol mixtures of increasing ethanol content as the eluant. The fractions eluted with ethyl acetate/ethanol (4:1) are combined and concentrated by evaporation. The residue is crystallised from ethyl acetate/petroleum ether to obtain 6-phenyl-8-chloro-4H-s-triazolo[4,3-a] [1,4]benzodiazepine-1-carboxaldehyde, M.P. 161°-163°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04002764
출처 데이터셋uspto-grants-1977_01
ORD IDord-ebe97f1dc49447a3b1dc27d7a0db5031
출처 메모uspto-grants-1977_01