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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897756Generated: October 30, 2026

4-Fluoro-2-methylbenzenesulfonyl chloride → N-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-fluoro-2-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1897756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-2-methylbenzenesulfonyl chlorideHCID 2778602—
Reactant4-(5-Amino-pyridin-3-yl)-2-chloro-benzonitrileHCID 59578390—
SolventPyridineHCID 1049—
ProductN-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-fluoro-2-methyl-benzenesulfonamideHCID 4981966348.7%

Reaction Steps

According to General Sulfonylation Procedure 2 in Example 1, to a solution of 4-(5-amino-pyridin-3-yl)-2-chloro-benzonitrile (20 mg, 87 μmol, 1 eq) in anhydrous pyridine (500 μl) was added 4-fluoro-2-methyl-benzenesulfonyl chloride (14 μl, 96 μmol, 1.1 eq). The product was purified by precipitation in methanol and lyophilized to give N-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-fluoro-2-methyl-benzenesulfonamide (17 mg, >95% purity, yield: 48.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-f266f4f563324fe2a2f2c544d4a61496
Source noteuspto-grants-2013_08