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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378096Generated: October 31, 2026

Chloroacetic anhydride → HCID 22914481, compound

https://huagongshe.com/reaction/1378096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic anhydrideHCID 10946—
Reactant7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-carboxylic acid hydrazideHCID 54382386—
SolventDimethylformamideHCID 6228—
ProductHCID 22914481HCID 2291448153.3%

Reaction Steps

15.3 g (50 mmol) of 7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-carboxylic acid hydrazide were stirred at room temperature overnight in 160 ml of N,N-dimethylformamide with 9.41 g (55 mmol) of chloroacetic anhydride. After evaporating the solvent the residue was stirred at room temperature over the weekend with 100 ml of a 10% solution of phosphorus pentoxide in methanesulphonic acid. The reaction mixture was treated with ice, made alkaline with conc. sodium hydroxide solution and extracted four times with methylene chloride. By drying the organic phase over magnesium sulfate, evaporation of the solvent and chromatography of the residue on silica gel while eluting with ethyl acetate there were obtained 9.7 g (53%) of 7-chloro-3-(5-chloromethyl-1,3,4-oxadiazol-2-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one of m.p. 201°-203°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-f41fdb2ffbaf4857aa3dd9e5c86d577f
Source noteuspto-grants-1997_09