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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605031Generated: November 1, 2026

1,2-Dichloroethane → 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carbonitrile

https://huagongshe.com/reaction/1605031

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carboxamideHCID 21486018—
SolventDimethylformamideHCID 6228—
Product6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carbonitrileHCID 12562499—

Reaction Steps

4 ml of phosphorous oxychloride is added to a solution of 1.69 g (0.005 mole) of 6-phenyl-8-chloro-4H-s-triazolo[4,3-a] [1,4]benzodiazepine-1-carboxamide in 5 ml of dimethylformamide, and stirring maintained for 10 minutes at 80°. The reaction mixture is then poured on ice and extraced with ethylene chloride. The extract is washed with water and saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evaporation. The residue is chromatographed on silica gel with the use of benzene and benzene/ethyl acetate mixtures as eluant. The fractions containing the desired nitrile [Rf = 0.5 in the eluant system benzene/chloroform/ethyl acetate (4:4:2)] are combined and concentrated by evaporation. The residue is crystallised from ethyl acetate/petroleum ether to obtain 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carbonitrile, M.P. 191°-192°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03948931
Source datasetuspto-grants-1976_04
ORD IDord-b15c3bc5530d4a6785fd7433d3de26d2
Source noteuspto-grants-1976_04