Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971630Generated: November 1, 2026

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

https://huagongshe.com/reaction/1971630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
SolventPyridineHCID 1049—
ProductN-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamideHCID 57607460—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Amino-5-fluoropyridine (4.0 g, 0.036 mol) was dissolved in pyridine (40 mL) and p-toluenesulfonyl chloride (7.5 g, 0.039 mol) was added. The reaction was heated at 80° C. for 24 hours then cooled and the pyridine was removed under vacuum. The residue was partioned between water (100 mL) and ethyl acetate (100 mL). The layers were separated and the organic layer was washed (3×100 mL) with water then dried and solvent stripped to give clean N-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamide 1 Rf 0.42, 50% E/H; MS m/z 267 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431608B2
Source datasetuspto-grants-2013_04
ORD IDord-2c6765f9cf1a419c9e947b6f06cdc0a2
Source noteuspto-grants-2013_04