Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22866Generated: October 27, 2026

Methanesulfenyl chloride, trifluoro- → 1-(2,6-Dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfenyl-5-(pyrazin-2-ylmethylamino)pyrazole

https://huagongshe.com/reaction/22866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2,6-Dichloro-4-trifluoromethylphenyl)-5-(pyrazin-2-ylmethylamino)pyrazoleHCID 22591646—
SolventDichloromethaneHCID 6344—
Product1-(2,6-Dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfenyl-5-(pyrazin-2-ylmethylamino)pyrazoleHCID 22591644—

Reaction Steps

To a solution of 3.0 g of 1-(2,6-dichloro-4-trifluoromethylphenyl)-5-(pyrazin-2-ylmethylamino)pyrazole dissolved in 30 ml of dried methylene chloride under a nitrogen atmosphere was added 14 ml of dried methylene chloride solution of trifluoromethylsulfenyl chloride at room temperature over about 1 hour, followed by stirring overnight. Saturated aqueous sodium hydrogen carbonate solution was added thereto, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and water several times. Thereafter, the layer was purified by a silica gel column chromatography. After removal of solvent, drying in vacuo afforded 3.59 g of 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfenyl-5-(pyrazin-2-ylmethylamino)pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849633B2
Source datasetuspto-grants-2005_02
ORD IDord-bd89ebcad29448aa87d9d887ef9be4bb
Source noteuspto-grants-2005_02