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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847468Generated: October 31, 2026

4-Amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one → HCID 14677257, compound

https://huagongshe.com/reaction/847468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 575002—
Reactant2-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 2777215—
SolventPyridineHCID 1049—
ProductHCID 14677257HCID 1467725780%

Reaction Conditions

Temperature-10 °C

Reaction Steps

10.0 g (0.088 mol) of 4-amino-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one are dissolved in 50 ml of dry pyridine, the mixture is cooled to -10° C., and 32.7 g (0.12 mol) of 2-trifluoromethoxy-benzenesulphonyl chloride are added. The reaction mixture is allowed to reach room temperature (approximately 20° C.) and stirred for approximately 12 hours. After the mixture has been concentrated, the residue is taken up in methylene chloride and shaken with 1N hydrochloric acid and then with water. The organic phase is dried with sodium sulfate and filtered. The solvent is carefully distilled off from the filtrate under a water pump vacuum. 23.1 g (80% of theory) of 4-(2-trifluoromethoxy-phenylsulphonylamino)-5-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one are obtained as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142060
Source datasetuspto-grants-1992_08
ORD IDord-01560cbef84b4a6883d5370c1e39113a
Source noteuspto-grants-1992_08