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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692252Generated: November 1, 2026

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

https://huagongshe.com/reaction/1692252

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 numberUS08153814B2
Source datasetuspto-grants-2012_04
ORD IDord-c0a19021d98646318b367959858e4bd9
Source noteuspto-grants-2012_04