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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897752Generated: October 29, 2026

4-Fluorobenzenesulfonyl chloride → N-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/1897752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant4-(5-Amino-pyridin-3-yl)-2-chloro-benzonitrileHCID 59578390—
SolventPyridineHCID 1049—
ProductN-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-fluoro-benzenesulfonamideHCID 4981952840%

Reaction Steps

According to general 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-benzenesulfonyl chloride (18.6 mg, 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-benzenesulfonamide (13.5 mg, >95% purity, yield: 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-2a0bbaa7e96643b1bdd21dfd5ffaab3f
Source noteuspto-grants-2013_08