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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644625Generated: November 1, 2026

Pyridine → 4-Bromo-2-fluoro-N-thiazol-2-yl-benzenesulfonamide

https://huagongshe.com/reaction/1644625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
ReactantDichloromethaneHCID 6344—
Reactant4-Bromo-2-fluorobenzene-1-sulfonyl chlorideHCID 2736310—
Product4-Bromo-2-fluoro-N-thiazol-2-yl-benzenesulfonamideHCID 2513835336%

Reaction Steps

To a solution of 2-aminothiazole (4.51 g, 0.0450 mol) and pyridine (24.26 mL, 0.3000 mol) in methylene chloride (40 mL, 0.6 mol) at 0° C. was added portionwise 4-bromo-2-fluorobenzenesulfonyl chloride (8.2 g, 0.030 mol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, diluted with EtOAc, washed with 1N HCl solution, H2O and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated to give the crude product that was purified via automated flash chromatography (silica gel, 25% EtOAc in hexanes to 100% EtOAc) to give the product as a light brown solid (3.6 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124610B2
Source datasetuspto-grants-2012_02
ORD IDord-a7de876b12d84a268667377c93faf3d1
Source noteuspto-grants-2012_02