Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764514Generated: October 26, 2026

Hydrazine hydrate (1:1) → Alprazolam

https://huagongshe.com/reaction/1764514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-Desmethyl-N(4)-desoxychlordiazepoxideHCID 165626—
Reactant2-Methylimidazole hydrochlorideHCID 521629—
ReactantEthyl ortho-acetateHCID 86598186—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductAlprazolamHCID 2118—

Reaction Steps

To a suspension of 1.35 parts of 2-amino-7-chloro-5-phenyl-3H-1,4-benzodiazepine in 25 parts by volume of methanol are added 0.6 part of 2-methylimidazole hydrochloride and 6 parts by volume of 1 mole methanol solution of hydrazine hydrate. The mixture is stirred at room temperature for 1.5 hours, followed by addition of 4.8 parts of ethyl orthoacetate and 10 parts by volume of ethanol containing 10% hydrogen chloride. The mixture is refluxed for 30 minutes, followed by evaporation of the solvent. The residue is neutralized with saturated aqueous sodium bicarbonate and extracted with methylene chloride. The methylene chloride extract is washed with water and dried over sodium sulfate, followed by evaporation of the solvent. The residue is purified by means of silica gel column-chromatography to give 8-chloro-1-methyl-6-phenyl-4H-s-triazolo [4,3-a][1,4] benzodiazepine. Recrystallization from a mixture of acetone and n-hexane affords colorless needles. Melting point: 225° C to 226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116956
Source datasetuspto-grants-1978_09
ORD IDord-6b343a50e8d947faa2445817e7501c13
Source noteuspto-grants-1978_09