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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473941Generated: October 30, 2026

4-Toluenesulfonyl chloride → N-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamide

https://huagongshe.com/reaction/1473941

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
SolventPyridineHCID 1049—
ProductN-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamideHCID 57607460100.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-amino-5-fluoropyridine (25 g, 0.22 mol) in pyridine (100 mL) was treated portion wise with p-toluenesulfonyl chloride (47.5 g, 0.25 mol) and heated at 80° C. for 2 hours. The cooled material was concentrated to remove the majority of pyridine. The resulting viscous solution was diluted with 200 ml of ethyl acetate then 200 ml of water. The resulting suspension was stirred for about an hour to break up the solids then filtered. The filter cake was washed with water then cold ethyl acetate, dried to afford 59 g of a light brown solid. Rf 0.43, 50% ethyl acetate/hexanes; MS m/z 266 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018208B2
Source datasetuspto-grants-2015_04
ORD IDord-b909c26ca76d47ed948027815c5fb180
Source noteuspto-grants-2015_04