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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 4362726 | HCID 4362726 | — |
| Reactant | HCID 178418311 | HCID 178418311 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-[1-(2,4-Dichlorophenoxy)ethyl]-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753665 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-4f36e255efb64a5483ec38ca23ccfbd9 |
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| Source note | uspto-grants-1998_05 |
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