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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378000Generated: November 1, 2026

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

https://huagongshe.com/reaction/1378000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodiumHCID 5360545—
Reactant(S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carbonitrileHCID 22876618—
SolventMethanolHCID 887—
Product(S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto-[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamidoximeHCID 54513121100%

Reaction Steps

0.60 g (26 mmol) of sodium was dissolved in 32 ml of methanol. 1.95 g (28.1 mmol) of hydroxylamine hydrochloride and, after 1 hour, 5.77 g (346 mmol) of (S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carbonitrile were added at room temperature. The suspension was stirred at 70° for 3.5 hours, cooled to 0° during 30 min. and the crystals were filtered off. By drying the crystallizate there were obtained 6.5 g (100%) of (S)-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxamidoxime of m.p. 248°-250°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-64c7e4e024554bcca9a1ace56cb5b8da
Source noteuspto-grants-1997_09