Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414905Generated: October 25, 2026

Ammonia → 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carboxamide

https://huagongshe.com/reaction/1414905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDichloromethaneHCID 6344—
ReactantSodium CyanideHCID 8929—
Reactant6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehydeHCID 21486011—
CatalystHCID 178418406HCID 178418406—
SolventIsopropanolHCID 3776—
Product6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carboxamideHCID 21486018—

Reaction Steps

0.245 g (0.005 mole) of sodium cyanide is added at 0°, with stirring, to the saturated solution of ammonia in 15 ml of isopropanol. After 5 minutes, a solution of 0.322 g (0.001 mole) of 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde in ca. 10 ml of isopropanol is added together with 0.87 g of manganese dioxide. After a further 10 minutes, another addition is made of 0.87 g (total 0.02 mole) of manganese dioxide, and the mixture stirred for 4 hours at 0°. After the addition of ca. 40 ml of methylene chloride, the reaction mixture is filtered and the filtrate concentrated by evaporation. Crystallisation of the residue from methanol/ethyl acetate/petroleum ether yields 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxamide, M.P. 285°-289°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002764
Source datasetuspto-grants-1977_01
ORD IDord-0e7597d4961c4450a9ef7f4f5254d266
Source noteuspto-grants-1977_01