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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382712Generated: October 26, 2026

Pyridine → 5-bromo-4-chloro-2-fluoro-N-methyl-N-pyridin-2-yl-benzenesulfonamide

https://huagongshe.com/reaction/2382712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium HydroxideHCID 14798—
Reactant2-Pyridinamine, N-methyl-HCID 20727—
Reactant5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chlorideHCID 56604734—
SolventDichloromethaneHCID 6344—
Product5-bromo-4-chloro-2-fluoro-N-methyl-N-pyridin-2-yl-benzenesulfonamideHCID 6847218831%

Reaction Steps

To 5-bromo-4-chloro-2-fluorobenzenesulfonyl chloride (1.5 g, 4.89 mmol) in dry DCM (15 mL), at −20° C. was added pyridine (1.98 mL, 24.5 mmol) followed by methyl-pyridin-2-yl-amine (1.06 g, 9.78 mmol). The mixture was allowed to warm slowly to ambient temperature over 16 hrs. 1N NaOH solution (5 mL) was added and stirred for 15 mins. The mixture was extracted with DCM and the organics were washed with brine, dried over MgSO4 and the filtrate evaporated. The residue was purified by silica gel chromatography [eluent: 10% ethyl acetate in hexane] to give 5-bromo-4-chloro-2-fluoro-N-methyl-N-pyridin-2-yl-benzenesulfonamide as an oil (0.57 g, 31%). MS: 380.9 (M+H)+; tR=2.80 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263588B2
Source datasetuspto-grants-2012_09
ORD IDord-4ad13fbee55b4c2ea65ada6207b94f58
Source noteuspto-grants-2012_09