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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897753Generated: October 30, 2026

4-Ethylbenzene-1-sulfonyl chloride → N-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-ethyl-benzenesulfonamide

https://huagongshe.com/reaction/1897753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethylbenzene-1-sulfonyl chlorideHCID 570959—
Reactant4-(5-Amino-pyridin-3-yl)-2-chloro-benzonitrileHCID 59578390—
SolventPyridineHCID 1049—
ProductN-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-ethyl-benzenesulfonamideHCID 4981952941.4%

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-ethyl-benzenesulfonyl chloride (15.5 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-ethyl-benzenesulfonamide (14.3 mg, >95% purity, yield: 41.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-79606644c21744c19c6327cb89604270
Source noteuspto-grants-2013_08