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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110674Generated: November 2, 2026

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

https://huagongshe.com/reaction/1110674

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 1N 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 numberUS04976773
Source datasetuspto-grants-1990_12
ORD IDord-4dd32cb082864481a5ad96100b6af56c
Source noteuspto-grants-1990_12