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HRID 67320作成日:2026年10月24日

Potassium Cyanide → methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate

https://huagongshe.com/ja/reaction/67320

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CyanideHCID 9032—
反応物Ro 14-7437HCID 127597—
溶媒MethanolHCID 887—
生成物methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylateHCID 10378479—

反応手順

285 mg (1 mmol) of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate and 66 mg of potassium cyanide are heated to boiling under reflux for 24 hours in 10 ml of methanol. Then, the mixture is concentrated on a rotary evaporator, the residue is partitioned between water and chloroform, extracted twice with chloroform, the chloroform phase is dried over magnesium sulphate and evaporated. There is obtained methyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 212°-214° C. This product is uniform according to thin-layer chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346030
出典データセットuspto-grants-1982_08
ORD IDord-2343817238154b91a71b7b1a643bedcf
出典メモuspto-grants-1982_08