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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378093Generated: October 31, 2026

Chloroacetic anhydride → HCID 22914464, compound

https://huagongshe.com/reaction/1378093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic anhydrideHCID 10946—
ReactantHCID 67713563HCID 67713563—
SolventDimethylformamideHCID 6228—
ProductHCID 22914464HCID 2291446461%

Reaction Steps

9.4 g (34.7 mmol) of 5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid hydrazide were stirred at room temperature for 3 hours in 75 ml of N,N-dimethyl- formamide with 27.1 g (41.5 mmol) of chloroacetic anhydride. After evaporating the solvent the residue was stirred at room temperature overnight with 75 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 6.9 g (61%) of 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. 221°-222°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-fa111943f86547f4904076e59292fd5d
Source noteuspto-grants-1997_09