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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764511Generated: October 25, 2026

Hydrazine hydrate (1:1) → Estazolam

https://huagongshe.com/reaction/1764511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-Desmethyl-N(4)-desoxychlordiazepoxideHCID 165626—
Reactant2-Methylimidazole hydrochlorideHCID 521629—
ReactantEthylorthoformateHCID 53630039—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductEstazolamHCID 3261—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116956
Source datasetuspto-grants-1978_09
ORD IDord-90dc2169421a4860a727a7fea7cdd172
Source noteuspto-grants-1978_09