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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401955Generated: October 31, 2026

Pyridine → 3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/1401955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
Reactant3,4-Difluorobenzene-1-sulfonyl chlorideHCID 2736913—
SolventDichloromethaneHCID 6344—
Product3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamideHCID 53513979—

Reaction Steps

To a slurry of 2-aminothiazole (23.88 g, 0.2384 mol) in methylene chloride (150 mL) and pyridine (38.0 mL, 0.470 mol) was added dropwise a solution of 3,4-difluorobenzenesulphonyl chloride (25.0 g, 0.118 mol) in 10 mL of methylene chloride. After stirring for 48 hours the reaction was diluted with more dichloromethane and extracted with 1N HCl. The organic layer was dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography to give 3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamide as a white solid. LCMS Rt=1.24 minutes MS m/z 277 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-b5c2af734f0641cfb376789d7a94e37c
Source noteuspto-grants-2014_12