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HRID 67409作成日:2026年10月24日

4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one → 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde

https://huagongshe.com/ja/reaction/67409

反応式

関与物質

役割名称HCID仕込み量
反応物4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851602—
触媒HCID 178418406HCID 178418406—
溶媒DichloromethaneHCID 6344—
生成物5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehydeHCID 19833020—

反応手順

A mixture of 12.2 g (50 mmol) of 4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one, 80.0 g of manganese dioxide and 500 ml of absolute methylene chloride is stirred at room temperature for 1 hour under an argon atmosphere and subsequently the manganese dioxide is filtered off under suction over Dicalit while rinsing with methylene chloride. The filtrate is evaporated to dryness in vacuo. After warming the residue in ca 150 ml of ethyl acetate, there is obtained 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde of melting point 205°-207° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346032
出典データセットuspto-grants-1982_08
ORD IDord-9abf338d25d0462aa945498e427d7c28
出典メモuspto-grants-1982_08