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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043742Generated: October 30, 2026

Triethylamine → N,N-dimethyl-3-(trifluoromethyl)-1H-pyrazole-1-sulfonamide

https://huagongshe.com/reaction/2043742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylsulphamoyl chlorideHCID 83372—
Reactant3-(Trifluoromethyl)pyrazoleHCID 1807034—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN,N-dimethyl-3-(trifluoromethyl)-1H-pyrazole-1-sulfonamideHCID 6682646799.5%

Reaction Steps

To a solution of 3-trifluoromethylpyrazole (5.0 g, 36 mmol), triethylamine (7.0 mL, 50 mmol) in dichloromethane (40 mL) was added N,N-dimethylsulfamoyl chloride (5.5 mL, 51 mmol) and the reaction mixture was warmed to reflux for 2 days. The reaction mixture was cooled to ambient temperature and filtered through a pad of silica gel using dichloromethane as an eluent. The resulting solution was then concentrated under reduced pressure to give an amber residue. The residue was dissolved in diethyl ether and washed with water. The extract was then dried over MgSO4 and concentrated under reduced pressure giving 8.71 g of the title compound. This compound was of sufficient purity to use in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-74f3d489e48946359fd7a21fe4626a02
Source noteuspto-grants-2013_11