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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502988Generated: November 4, 2026

Hydrochloric Acid → HCID 11515798, compound

https://huagongshe.com/reaction/502988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68468835HCID 68468835—
SolventChloroformHCID 6212—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 11515798HCID 11515798—

Reaction Conditions

Temperature80 °C

Reaction Steps

Acetic anhydride (0.19 ml) and N,N-dimethylaminopyridine (40 mg) were added to a pyridine (10 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 4 days. After the reaction solution and chloroform were added to a 1M hydrochloric acid solution, 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 96:4) and then the resulting solid was washed with ether to obtain 393 mg of N-{1-methyl-1-[4-methyl-5-(2-methylphenyl)-4H-1,2,4-triazol-3-yl]ethyl}-N-phenylacetamide (pale yellow solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-dd248c5b0a404656945655491997443f
Source noteuspto-grants-2010_08