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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325029Generated: October 29, 2026

Pyridine → N-{3-[2-(4-Cyanophenyl)ethoxy]phenyl}-2-chlorobenzenesulfonamide

https://huagongshe.com/reaction/325029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantHCID 22033543HCID 22033543—
SolventDichloromethaneHCID 6344—
ProductN-{3-[2-(4-Cyanophenyl)ethoxy]phenyl}-2-chlorobenzenesulfonamideHCID 1087335636.6%

Reaction Steps

Pyridine (0.255 mL; 3.15 mmol) was added to a stirred solution of amino-3-[2-(4-cyanophenyl)ethoxy]benzene (0.15 g; 0.629 mmol; from step (ii) above) and 2-chlorobenzenesulfonyl chloride (0.173 mL; 0.818 mmol) in CH2Cl2 (4 mL). After 45 minutes at room temperature the solvent was removed in vacuo. To remove traces of pyridine, EtOH was added and evaporated. The residue was partitioned between water and EtOAc. The organic layer was washed with 0.1M aqueous HCl and brine, dried (Na2SO4) and the solvent removed in vacuo. Purification by flash chromatography (SiO2; toluene:EtOAc (1:0 to 9:1)) afforded 0.095 g (35%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-b9229219405c4f0388bd3991ce3d5146
Source noteuspto-grants-2001_04