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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591016Generated: November 1, 2026

Sulfanilamide → 4-(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propanamido)benzenesulfonamide

https://huagongshe.com/reaction/1591016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfanilamideHCID 5333—
ReactantTriethylamineHCID 8471—
Reactant4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxypropionic acid chloride hydrochlorideHCID 88451402—
SolventTetrahydrofuranHCID 8028—
Product4-(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propanamido)benzenesulfonamideHCID 1449855480.8%

Reaction Steps

(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride (0.8 g) and 4-aminobenzene sulfonamide (0.5 g) were dissolved in dry tetrahydrofuran (20 ml), and the solution was stirred, with an addition of triethylamine (0.6 ml) at room temperature for 2 hours. After completion of the reaction, the solvent was evaporated under a reduced pressure, the residue was dissolved in methylene chloride and washed with 1 N hydrochloric acid, water, saturated aqueous sodium hydrogen carbonate, water and saturated aqueous sodium chloride After drying over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under a reduced pressure was purified by medium pressure column chromatography by using silica gel, to obtain the title compound (0.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05205855
Source datasetuspto-grants-1993_04
ORD IDord-36f182a8739449d2acf0bf3152953ca8
Source noteuspto-grants-1993_04