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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414911Generated: November 1, 2026

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

https://huagongshe.com/reaction/1414911

Reaction equation

Participants

RoleNameHCIDCharge
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 phosphorus 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 5ml of dimethylformamide, and stirring maintained for 10 minutes at 80°. The reaction mixture is then poured on ice and extracted 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 numberUS04002764
Source datasetuspto-grants-1977_01
ORD IDord-48e8614f3f5146228323afa1b74e86f7
Source noteuspto-grants-1977_01