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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438646Generated: November 1, 2026

2-[5-Chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl]benzoic acid → 2-[5-Chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl]benzoic acid methyl ester

https://huagongshe.com/reaction/1438646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[5-Chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl]benzoic acidHCID 11656531—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
SolventMethanolHCID 887—
Product2-[5-Chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl]benzoic acid methyl esterHCID 57942092—

Reaction Steps

A mixture of 2-[5-chloro-3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyridine-2-carbonyl]benzoic acid (20 mg), 4N HCl/dioxane (1 mL) and 1.5 mL of methanol was refluxed overnight. After cooled to room temperature, the mixture was concentrated and the residue was diluted with ethyl acetate, washed with sodium bicarbonate and brine and dried. Removal of the solvents afforded the title compound as an off white solid: 1H NMR: (CDCl3, ppm) δ 11.20 (s, 1 H), 8.22 (m, 2H), 8.04 (m, 2H), 7.94 (m, 1 H), 7.62 (m, 2H), 7.54 (m, 1 H), 7.31 (m, 1 H), 3.54 (s, 3H); MS: (M+H)/z=533.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622583B2
Source datasetuspto-grants-2009_11
ORD IDord-2212aa0710ae4fb889071f6c77734a35
Source noteuspto-grants-2009_11