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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 267224생성일: 2026년 10월 26일

Hydrogen Bromide → alpha-Hydroxyalprazolam

https://huagongshe.com/reaction/267224

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물1-(benzyloxymethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 20473083—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
생성물alpha-HydroxyalprazolamHCID 162244—

반응 단계

An amount of 25 g of 1-(benzyloxymethyl)-6-phenyl- 8-chloro-4H-s-triazolo[4,3-a] [1,4]benzodiazepine is dissolved in 200 ml of glacial acetic acid; there is then added to the solution 170 ml of 48% aqueous hydrobromic acid. The mixture is heated for 90 minutes at 80° and then cooled to 5°; while stirring is maintained, the mixture is adjusted to pH 6 with concentrated sodium hydroxide solution, and water as well as methylene chloride subsequently added. The organic phase is separated, washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated by evaporation. The residue is dissolved in ethyl acetate/methanol (9:1); the solution is filtered through a column of 150 g of silica gel (Merck, particle size 0.05 - 0.2 mm), and the column eluted with ethyl acetate/methanol (9:1) to (7:3). The eluate is concentrated by evaporation and the residue crystallised from ethyl acetate/ether to obtain 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-methanol, M.P. 210°-211°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03941799
출처 데이터셋uspto-grants-1976_03
ORD IDord-371e4044eee94e0d84a1b04546d397dd
출처 메모uspto-grants-1976_03