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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377988Generated: November 1, 2026

Hydrochloric Acid → (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid

https://huagongshe.com/reaction/1377988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactantethyl (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]-benzodiazepine-1-carboxylateHCID 54090463—
SolventWaterHCID 962—
Product(S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acidHCID 2282178191%

Reaction Steps

57.3 g (164 mmol) of ethyl (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]-benzodiazepine-1-carboxylate, 40 ml of ethanol, 60 ml of water and 51.5 ml (206 mmol) of 4N sodium hydroxide solution were heated to reflux on a steam bath for 30 min. The alcohol was evaporated on a rotary evaporator. The aqueous phase remaining behind was washed twice with methylene chloride and acidified to pH 3-4 with 51.5 ml (206 mmol) of 4N hydrochloric acid. The suspension obtained was cooled and filtered, and the filter residue was washed with a small amount of ice-water and dried. There were obtained 47.92 g (91%) of (S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid of m.p. 225°-226°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-050df39375aa439085c33495082d7a1f
Source noteuspto-grants-1997_09