Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635918Generated: October 31, 2026

Hydrochloric Acid → HCID 22136182, compound

https://huagongshe.com/reaction/1635918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazineHCID 1502563—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
ProductHCID 22136182HCID 22136182—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 6-Chloro-3-phenyl-1,2,4-Triazolo[3,4-a]phthalazine (2.0 g, prepared according to procedures described in Zh. Org. Khim. (1975), 11(7), 1570-2 and J. Med. Chem. (1988),31(6), 1115-23.) and copper cynaide (2.0 g) in 50 ml of DMSO is stirred at 140° C. overnight. The mixture is cooled, poured into water and extracted with methylene chloride. The organic layer is washed with water, dried over Na2SO4 and concentrated to give a tan solid which is then dissolved in 50 mL of methanol. The resulting solution is saturated with HCl gas and the mixture is stirred at room temperature overnight. 20 mL of water and 1 mL of 10 N NaOH solution are added, the resulting mixture is then heated under reflux for 4 hours. The methanol is then evaporated in vacuo, and the remaining mixture is diluted with water. After adjusting the pH to 4-5 with 1N HCl , the solid is collected by filtration, and dried to give the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511987B1
Source datasetuspto-grants-2003_01
ORD IDord-18dd4744d54e426fbc3f30f0ddf5bd2c
Source noteuspto-grants-2003_01