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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22765Generated: October 26, 2026

4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chloride → 4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/22765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Chloro-2-cyanophenoxy)benzenesulfonyl chlorideHCID 2776917—
ReactantBenzenamine, 3-[2-(dimethylamino)ethoxy]-4-(trifluoromethyl)-HCID 17756283—
SolventChloroformHCID 6212—
Product4-(3-chloro-2-cyano-phenoxy)-N-[3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenyl]-benzenesulfonamideHCID 10165761—

Reaction Steps

To a mixture of 3-(2-dimethylamino-ethoxy)-4-trifluoromethyl-phenylamine (0.10 g, 0.4 mmol) in CHCl3 (2.5 mL) was added 4-(3-chloro-2-cyano-phenoxy) benzenesulfonyl chloride (0.13 g, 0.4 mmol) at rt. After stirring at rt for 72 h, the solvent was evaporated and the residue was purified by vacuum filtration through silica gel eluting successively with 4% MeOH in CH2Cl2 and 10% MeOH in CH2Cl2 followed by a mixture of CH2Cl2, MeOH and conc. NH4OH (90:10:1). The solvent was removed from the desired fractions and the residue was recrystallized from a mixture of MeOH and EtOAc to afford the title compound as a white solid; yield 0.01 g (5%): LCMS 540 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849635B2
Source datasetuspto-grants-2005_02
ORD IDord-f654829ee46b47468eb0b6f8ed977fb2
Source noteuspto-grants-2005_02