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HRID 268029作成日:2026年10月27日

Phosphoric Acid → 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde-diethylacetal

https://huagongshe.com/reaction/268029

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物p-Toluenesulfonic acidHCID 6101—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物alpha-HydroxyalprazolamHCID 162244—
溶媒Dimethyl SulfoxideHCID 679—
溶媒EthanolHCID 702—
溶媒DichloromethaneHCID 6344—
生成物6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde-diethylacetalHCID 21553106—

反応手順

A mixture of 300 mg of 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-methanol, 0.57 g of dicyclohexyl-carbodiimide, 45 mg of phosphoric acid and 3 ml of abs. dimethylsulphoxide is stirred for 6 days at 25° and for a further 2 days at 70°-80°. Methylene chloride is then added, the organic phase washed with water and saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evarporation. Crude 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde is obtained, which is dissolved in 5 ml of ethanol. An addition is made to the obtained solution of 100 mg of p-toluenesulphonic acid, and the mixture refluxed for 10 hours. The solution is concentrated in vacuo. The residue is taken up in methylene chloride, the organic phase washed with 5% aqueous potassium carbonate solution and with saturated sodium chloride solution, dried over sodium sulphate, and concentrated by evaporation. The residue is recrystallised from ethyl acetate/ether/petroleum ether to obtain 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde-diethylacetal, M.P. 133°-135°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03946032
出典データセットuspto-grants-1976_03
ORD IDord-1510bf09485843ca938db78524887de5
出典メモuspto-grants-1976_03