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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1764511생성일: 2026년 10월 26일

Hydrazine hydrate (1:1) → Estazolam

https://huagongshe.com/reaction/1764511

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물N-Desmethyl-N(4)-desoxychlordiazepoxideHCID 165626—
반응물2-Methylimidazole hydrochlorideHCID 521629—
반응물EthylorthoformateHCID 53630039—
용매EthanolHCID 702—
용매MethanolHCID 887—
생성물EstazolamHCID 3261—

반응 단계

To a suspension of 8.1 parts of 2-amino-7-chloro-5-phenyl-3H-1,4-benzodiazepine in 180 parts by volume of methanol are added 3.6 parts of 2-methylimidazole hydrochloride and 2.25 parts by volume of 80% hydrazine hydrate. The suspension is stirred at room temperature for 1.5 hours, and then 25 parts of ethyl orthoformate is added. To the mixture is added dropwise with stirring 60 parts by volume of ethanol containing 10% hydrogen chloride. After stirring for a further 1 hour, the mixture is warmed for a while so as to complete the reaction. After evaporation of the solvent, an aqueous solution of sodium bicarbonate is added to the residue to neutralize it. The mixture is then extracted with methylene chloride. The methylene chloride layer is washed with water and dried over sodium sulfate, followed by evaporation of the solvent. The residue is recrystallized from a mixture of acetone and n-hexane to give 8-chloro-6-phenyl-4H-s-triazolo [4,3-a][1,4] benzodiazepine as colorless flakes. Melting point; 226° C to 227° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04116956
출처 데이터셋uspto-grants-1978_09
ORD IDord-90dc2169421a4860a727a7fea7cdd172
출처 메모uspto-grants-1978_09