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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26116Generated: October 26, 2026

Diethylcarbamoyl chloride → 1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole

https://huagongshe.com/reaction/26116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
ReactantTriethylamineHCID 8471—
ReactantHCID 178457344HCID 178457344—
SolventTetrahydrofuranHCID 8028—
Product1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazoleHCID 21324268—

Reaction Steps

A mixture of 6.9 g. 3-diallylsulphamoyl-1,2,4-triazole, 4.5 g. diethylcarbamoyl chloride, 6ml. triethylamine and 25 ml. dry tetrahydrofuran was refluxed under anhydrous conditions for 1.5 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated to remove solvent. The solid residue was recrystallized from petroleum ether, b.p. 60°-80° C., to give 1-diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole, m.p. 49°-51° C. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148626
Source datasetuspto-grants-1979_04
ORD IDord-4267794288414405abf990af1d5262c8
Source noteuspto-grants-1979_04