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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360062Generated: November 1, 2026

Pyridine → N-(4-bromo-2-fluoro-5-methylphenyl)methanesulfonamide

https://huagongshe.com/reaction/2360062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Bromo-2-fluoro-5-methylanilineHCID 7018040—
SolventDichloromethaneHCID 6344—
ProductN-(4-bromo-2-fluoro-5-methylphenyl)methanesulfonamideHCID 6706653199.2%

Reaction Steps

To a solution of 4-bromo-2-fluoro-5-methylaniline (2.04 g, 10.0 mmol) in anhydrous CH2Cl2 (20 ml) and pyridine (3.23 ml, 40.0 mmol) was added methanesulfonyl chloride (0.86 ml, 11.0 mmol) and the resulting mixture was stirred at room temperature for 2 h. Solvent was removed in vacuo, and the residue was partitioned between EtOAc and 1M aq. HCl. The organic layer was washed with saturated aqueous NaHCO3, brine and then dried over Na2SO4. The drying agent was filtered off, and the filtrate was concentrated to give the title compound as a solid (2.80 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685991B2
Source datasetuspto-grants-2014_04
ORD IDord-5e516db28e5f47eaab15320aed9e4148
Source noteuspto-grants-2014_04