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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625981Generated: October 26, 2026

2,4-Difluorobenzenesulfonyl Chloride → N-(5-bromo-2-methoxypyridin-3-yl)-2,4-difluorobenzenesulfonamide

https://huagongshe.com/reaction/1625981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Difluorobenzenesulfonyl ChlorideHCID 2734273—
Reactant5-Bromo-2-methoxypyridin-3-amineHCID 44754869—
SolventPyridineHCID 1049—
ProductN-(5-bromo-2-methoxypyridin-3-yl)-2,4-difluorobenzenesulfonamideHCID 5985995131.7%

Reaction Steps

To a cooled (0° C.) solution of 5-bromo-2-(methyloxy)-3-pyridinamine (20.3 g, 100 mmol) in pyridine (200 mL) was added slowly 2,4-difluorobenzenesulfonyl chloride (21.3 g, 100 mmol) over 15 min (reaction became heterogeneous). The ice bath was removed and the reaction was stirred at ambient temperature for 16 h, at which time the reaction was diluted with water (500 mL) and the solids filtered off and washed with copious amounts of water. The precipitate was dried in a vacuum oven at 50° C. to give N-[5-bromo-2-(methyloxy)-3-pyridinyl]-2,4-difluorobenzenesulfonamide (12 g, 31.6 mmol, 31.7% yield) MS(ES)+ m/e 379.0, 380.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785433B2
Source datasetuspto-grants-2014_07
ORD IDord-893a48bf22d549f289c776fbb76dbbaf
Source noteuspto-grants-2014_07