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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290812Generated: October 30, 2026

HCID 4362726, compound → 7-[1-(2,4-Dichlorophenoxy)ethyl]-[1,2,4]triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1290812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 4362726HCID 4362726—
ReactantHCID 178418311HCID 178418311—
SolventAcetic AcidHCID 176—
Product7-[1-(2,4-Dichlorophenoxy)ethyl]-[1,2,4]triazolo[1,5-a]pyrimidineHCID 3801474—

Reaction Steps

A solution of 4-(2,4-dichlorophenoxy)-1-(dimethylamino)-1-penten-3-one (2.9 g) in glacial acetic acid (25 ml) was added to a stirred solution of 3-amino-1,2,4-triazole (0.93 g) also in glacial acetic acid (25 ml). The mixture was heated under reflux for 5 hours and then cooled to room temperature. The mixture was then poured into 200 ml of ice-water and extracted with toluene. The toluene extracts were washed with a 10% aqueous solution of sodium hydrogen carbonate followed by water, then dried over anhydrous magnesium sulphate and the solvent was evaporated under reduced pressure. The residue was triturated with cold diethyl ether and the solid was collected by filtration, followed by recrystallisation from a mixture of ethyl acetate and petroleum ether (b.p. 40°-60° C.) to give 7-[1-(2,4-dichlorophenoxy)ethyl]-1,2,4-triazolo[1,5-a]pyrimidine. Yield 2.02 g, (mp 137°-138° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753665
Source datasetuspto-grants-1998_05
ORD IDord-4f36e255efb64a5483ec38ca23ccfbd9
Source noteuspto-grants-1998_05