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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897751Generated: October 29, 2026

4-Methoxybenzenesulfonyl chloride → HCID 49819527, compound

https://huagongshe.com/reaction/1897751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
Reactant4-(5-Amino-pyridin-3-yl)-2-chloro-benzonitrileHCID 59578390—
SolventPyridineHCID 1049—
ProductHCID 49819527HCID 4981952743.1%

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, leg) in anhydrous pyridine (500 μl) was added 4-methoxy-benzenesulfonyl chloride (19.8 mg, 96 μmol, 1.1 eq). The crude product was purified by Isco Cornbiflash® Companion™ flash chromatography system on normal phase (4 g SiO2, flow rate 18 mL/min), eluting with mixtures of dichloromethane/methanol, to give N-[5-(3-chloro-4-cyano-phenyl)-pyridin-3-yl]-4-methoxy-benzenesulfonamide (15 mg, >95% purity, yield: 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-01a265499de2481493d78dc0f863b3dc
Source noteuspto-grants-2013_08