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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570998Generated: October 26, 2026

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

https://huagongshe.com/reaction/570998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
Reactant3-BromopyridineHCID 12286—
ReactantSodium hydrideHCID 24758—
ReactantDimethylsulphamoyl chlorideHCID 83372—
Reactant3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 67499540—
ReactantHCID 178478253HCID 178478253—
ProductN,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—
ProductHCID 178478253HCID 178478253—

Reaction Steps

US 20130288893(A1) describes, inter alia, certain (3-halo-1-(pyridin-3-yl)-1H-pyrazol-4-yl)amides and carbamates and their use as pesticides. The route to prepare such compounds involved the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine by the direct coupling of 3-bromopyridine with 3-chloropyrazole. The 3-chloropyrazole was prepared by a) treating 1H-pyrazole with 2 dimethylsulfamoyl chloride and sodium hydride to provide N,N-dimethyl-1H-pyrazole-1-sulfonamide, b) treating the N,N-dimethyl-1H-pyrazole-1-sulfonamide with perchloroethane and n-butyl lithium to provide 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide, and c) removing the N,N-dimethylsulfonamide from 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide with trifluoroacetic acid to give the 3-chloropyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024031B1
Source datasetuspto-grants-2015_05
ORD IDord-2a03cfb05023492ca6503b714575bfc6
Source noteuspto-grants-2015_05