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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409006Generated: October 30, 2026

Pyrazole → N,N-dimethyl-1H-pyrazole-1-sulfonamide

https://huagongshe.com/reaction/1409006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantSodium hydrideHCID 24758—
ReactantDimethylsulphamoyl chlorideHCID 83372—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (50%, 8.46 g) was added to a solution of pyrazole (12 g) in tetrahydrofuran (200 mL) while stirring at 0° C. After 20 min, dimethylsulfamoyl chloride (17 mL) was added dropwise, and the mixture was stirred at the same temperature for 1 hr and allowed to warm to room temperature over 1 hr. The reaction system was poured into saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (25.3 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921354B2
Source datasetuspto-grants-2014_12
ORD IDord-818b98a45c4b414b8441611e7effb045
Source noteuspto-grants-2014_12