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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897754Generated: October 27, 2026

4-Cyanobenzenesulfonyl chloride → N-[5-(3-Chloro-4-cyano-phenyl)-pyridin-3-yl]-4-cyano-benzene-sulfonamide

https://huagongshe.com/reaction/1897754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
Reactant4-(5-Amino-pyridin-3-yl)-2-chloro-benzonitrileHCID 59578390—
SolventPyridineHCID 1049—
ProductN-[5-(3-Chloro-4-cyano-phenyl)-pyridin-3-yl]-4-cyano-benzene-sulfonamideHCID 4981953039.4%

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-cyano-benzenesulfonyl chloride (19.3 mg, 96 μmol, 1.1 eq). The product was purified by preparative TLC, the plate was eluted with dichloromethane/methanol 95/5, to give (15.5 mg, >95% purity, yield: 39.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-301d01a4101f46bc8a19c76772365261
Source noteuspto-grants-2013_08