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HRID 1764514作成日:2026年10月27日

Hydrazine hydrate (1:1) → Alprazolam

https://huagongshe.com/reaction/1764514

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物N-Desmethyl-N(4)-desoxychlordiazepoxideHCID 165626—
反応物2-Methylimidazole hydrochlorideHCID 521629—
反応物Ethyl ortho-acetateHCID 86598186—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物AlprazolamHCID 2118—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04116956
出典データセットuspto-grants-1978_09
ORD IDord-6b343a50e8d947faa2445817e7501c13
出典メモuspto-grants-1978_09