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HRID 1764511作成日:2026年10月27日

Hydrazine hydrate (1:1) → Estazolam

https://huagongshe.com/reaction/1764511

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EthylorthoformateHCID 53630039—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物EstazolamHCID 3261—

反応手順

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.

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-90dc2169421a4860a727a7fea7cdd172
出典メモuspto-grants-1978_09