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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223197Generated: October 30, 2026

Ethanol → 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid

https://huagongshe.com/reaction/223197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantSarmazenilHCID 71231—
SolventWaterHCID 962—
Product7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acidHCID 14590421—

Reaction Steps

A mixture of 3.11 g (9.72 mmol) of ethyl 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate, 10 ml of ethanol, 2 ml of water and 400 mg of sodium hydroxide is heated to boiling under reflux for 1 hour. After evaporation of the ethanol, the residue is treated with 10 ml of 1 N hydrochloric acid. The colourless material obtained is filtered off under suction, washed with water and dried. There is obtained 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid with a decomposition point of 283°-284°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352818
Source datasetuspto-grants-1982_10
ORD IDord-04d660b749e44f96b13eb7d1e2871a9f
Source noteuspto-grants-1982_10