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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731515Generated: November 2, 2026

Ethanol → 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamidoxime

https://huagongshe.com/reaction/1731515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carbonitrileHCID 13984542—
SolventWaterHCID 962—
Product5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamidoximeHCID 56610303—

Reaction Steps

A mixture of 0.0125 mole 3-cyano-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine (prepared as in U.S. Pat. No. 4,316,839), 1.1 g of hydroxylamine hydrochloride, 200 ml of 99% ethanol and 5.2 ml of 20% potassium carbonate solution in water was heated with stirring for two hours. The reaction mixture was filtered and the filtrate was concentrated. The residue was treated with 100 ml of water and the crystalline solid was filtered off and washed with water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622321
Source datasetuspto-grants-1986_11
ORD IDord-3bf3b4cf87374648a0a3a543a506d24c
Source noteuspto-grants-1986_11