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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650795Generated: October 31, 2026

1H-1,2,4-Triazole → HCID 57132067, compound

https://huagongshe.com/reaction/1650795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-1-(5-chloropyridin-2-yl)ethan-1-oneHCID 23052498—
SolventAcetonitrileHCID 6342—
ProductHCID 57132067HCID 57132067—

Reaction Steps

5-Chloro-2-chloroacetylpyridine (20 g.) was dissolved in acetonitrile (25 ml.) and added dropwise to a refluxing solution of 1,2,4-triazole (6.2 g.) and potassium carbonate (13.4 g.) in acetonitrile (25 ml.). When the addition was complete, the solution was allowed to cool and was stirred for 2 hours. The solvent was evaporated and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated, washed twice with water and twice with brine, dried over sodium sulphate and filtered. The filtrate was evaporated to dryness under reduced pressure, and the residue was chromatographed on a K60 silica column, eluting with ethyl acetate, to give 5-chloropyrid-2-yl-1,2,4-triazol-1-ylmethyl ketone which after crystallisation from ethyl acetate/petroleum ether (b.p. 60°-80°), had m.p. 146°-148°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925863
Source datasetuspto-grants-1990_05
ORD IDord-2b5e18c6b85b4492b14aaeab6b66dbe8
Source noteuspto-grants-1990_05