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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654782Generated: October 30, 2026

Methanesulfonyl chloride → HCID 10042938, compound

https://huagongshe.com/reaction/654782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10546370HCID 10546370—
SolventPyridineHCID 1049—
ProductHCID 10042938HCID 1004293893.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]pyrazole-3-carboxamide (2.7 g) and methanesulfonyl chloride (3.4 ml) in pyridine (25 ml) was stirred at 50° C. for 6 hours. The solvent was evaporated, and ethyl acetate and water were added to the residue. The precipitates were filtered and washed with water and ethyl acetate. The filtrate was separated, and the organic layer was washed with dilute hydrochloric acid, dried and concentrated to dryness. The residue and the former precipitates were combined and recrystallized from a mixture of ethanol and ethyl acetate to give colorless crystals of 1-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]pyrazole-3-carbonitrile (2.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134142
Source datasetuspto-grants-1992_07
ORD IDord-c522c6e53dca4fb0b26740b64d8bd217
Source noteuspto-grants-1992_07