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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377991Generated: November 2, 2026

Hydroxyamine hydrochloride → (S)-8-chloro-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/1377991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodiumHCID 5360545—
Reactant(S)-8-chloro-7-fluoro-12,12a-dihydro-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carbonitrileHCID 54499997—
SolventMethanolHCID 887—
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-carboxamidoximeHCID 5400243497.5%

Reaction Steps

3.1 g (134.8 mmol) of sodium were dissolved in 140 ml of methanol. 10 g (145 mmol) of hydroxylamine hydrochloride and 28.6 g (94.5 mmol) 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-carbonitrile were added in succession at room temperature. The suspension was stirred at room temperature overnight, cooled to 0° during 30 min., the crystals were filtered off, suspended in 50 ml of water and filtered off. The methanol solution was concentrated, whereupon the residue was suspended in 30 ml of water and the crystals were filtered off. By drying the combined crystallizate there were obtained 30.94 g (97%) 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-carboxamidoxime of m.p. 236°-238°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-7f53eb4bcb4040e482db0fb134e8f286
Source noteuspto-grants-1997_09