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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378153Generated: November 2, 2026

Ammonia → (S)-7-fluoro-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide

https://huagongshe.com/reaction/1378153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]-benzodiazepine-1-carboxylic acidHCID 22828763—
SolventDimethylformamideHCID 6228—
Product(S)-7-fluoro-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamideHCID 2287661976%

Reaction Steps

100 g (348 mmol) of (S)-7-fluoro-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid were suspended in 600 ml of N,N-dimethylformamide and treated with 64.1 g (395 mmol) of 1,1'-carbonyldiimidazole. After stirring at 50° for 30 minutes 80 ml of 25% ammonia were added dropwise at 13° to 20° and the mixture was stirred for 30 minutes and poured into 21 of water. By suction filtration of the resulting suspension and drying the crystals there were obtained 52.7 g (76%) of (S)-7-fluoro-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamide of m.p. 223°-224°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-988b62287c3d45e49e10a08f11b49faa
Source noteuspto-grants-1997_09