Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438431Generated: November 2, 2026

3-Amino-2-bromo-5-chloropyridine → N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1438431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-2-bromo-5-chloropyridineHCID 2769640—
Reactant4-Chloro-3-(trifluoromethyl)benzenesulfonyl ChlorideHCID 2780719—
SolventPyridineHCID 1049—
ProductN-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-3-trifluoromethyl-benzenesulfonamideHCID 57942594—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (1.5 g, 5.3 mmol) and 2-bromo-5-chloro-pyridin-3-ylamine (500 mg, 2.4 mmol) dissolved in pyridine (20 mL) was heated at 60° C. for 16 h. The solvent was evaporated and the residue suspended in a 1:1 mixture of 2 M NaOH and methanol (20 mL) and heated at 70° C. for 30 min. The methanol was evaporated under reduced pressure and the residue diluted with 15 mL water. The solution was cooled on ice bath and the pH was adjusted to 3 by drop wise addition of concentrated HCl. The solid formed was collected by filtration and the product was purified by flash chromatography on silica gel column to afford the desired product. MS m/z: 450.8 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622583B2
Source datasetuspto-grants-2009_11
ORD IDord-82f162121469413b81f1a688d7aa05c1
Source noteuspto-grants-2009_11