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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867522Generated: October 30, 2026

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

https://huagongshe.com/reaction/867522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
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 37.3 g (116.6 mmol) of ethyl 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate, 5.276 g (131.9 mmol) of sodium hydroxide, 150 ml of ethanol and 100 ml of water is heated to boiling under reflux for 15 minutes. The mixture is then neutralized by the addition of 132 ml of 1N hydrochloric acid, the ethanol is distilled off in vacuo and the residue is diluted with 100 ml of water. The mixture is cooled to about 0°, the product is filtered off under suction, rinsed with water and dried at 80° in a high vacuum. There is obtained 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid of decomposition point 283°-284°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775671
Source datasetuspto-grants-1988_10
ORD IDord-705a3bfe427244c19dd243dfb7dfca2a
Source noteuspto-grants-1988_10