Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502987Generated: November 2, 2026

Hydrochloric Acid → HCID 68470278, compound

https://huagongshe.com/reaction/502987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 68468835HCID 68468835—
SolventChloroformHCID 6212—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68470278HCID 68470278—

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzoyl chloride (0.21 ml) and N,N-dimethylaminopyridine (40 mg) were added to a pyridine (15 ml) solution of N-{1-methyl-1-[4-methyl-5-(2-methylphenyl)-4H-1,2,4-triazol-3-yl]ethyl}aniline (500 mg), followed by stirring at 80° C. for 3 days. After the reaction solution and chloroform were added to 1M hydrochloric acid, the reaction solution and chloroform were added to brine and then the organic layer was separated. Furthermore, the organic layer washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated sodium chloride solution successively, dried over anhydrous magnesium-sulfate, and filtered and then the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by flash column chromatography (chloroform:methanol=99:1 to 98:2) and then the resulting solid washed with ether to obtain 523 mg of N-{1-methyl-1-[4-methyl-5-(2-methylphenyl)-4H-1,2,4-triazol-3-yl]ethyl}-N-phenylbenzamide (colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-21105205039b46c1850aaa33d0f11ff0
Source noteuspto-grants-2010_08