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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223211Generated: October 31, 2026

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

https://huagongshe.com/reaction/223211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantRo 14-7437HCID 127597—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acidHCID 10332676—

Reaction Steps

A solution of 14.26 g (0.05 mol) of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate and 2.2 g (0.055 mol) of sodium hydroxide in 100 ml of ethanol and 20 ml of water is heated to boiling under reflux for 45 minutes and subsequently treated with 55 ml of 1 N hydrochloric acid and 50 ml of water. After distilling off the ethanol, the resulting crystal slurry is filtered off under suction, washed with water and dried. There is obtained 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid of melting point 287°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352818
Source datasetuspto-grants-1982_10
ORD IDord-079a7f14a4ed48cea91835bd144fac0a
Source noteuspto-grants-1982_10