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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898803Generated: November 1, 2026

Acetic Acid → 2-Benzylthio-5-methoxy-7-methyl[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1898803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHexaneHCID 8058—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Benzylthio-5-chloro-7-methyl[1,2,4]triazolo[1,5-a]pyridineHCID 19080764—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-Benzylthio-5-methoxy-7-methyl[1,2,4]triazolo[1,5-a]pyridineHCID 19080776—

Reaction Steps

A mixture of 2-benzylthio-5-chloro-7-methyl[1,2,4]triazolo[1,5-a]pyridine (5.0 g, 0.017 mol), sodium methoxide in methanol (16 mL of 25 percent, 3.7 g, 0.070 mol) and methanol (100 mL) were heated at reflux with stirring for 4 hours. The reaction mixture was then cooled, acidified with acetic acid (10 mL), and concentrated by evaporation under reduced pressure. The residue obtained was dissolved in dichloromethane and the resulting solution was washed well with water, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The residue obtained was mixed with hexane and filtered to recover the solids. The solids were dried to obtain 4.7 g (97 percent of theory) of the title compound as a tan powder melting at 85°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571775
Source datasetuspto-grants-1996_11
ORD IDord-e6a07066be0f44eda8e0057a0a2373cd
Source noteuspto-grants-1996_11