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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252719Generated: November 1, 2026

4-Fluorobenzenesulfonyl chloride → N-(5-bromo-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/252719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant3-Amino-5-bromo-2-chloropyridineHCID 21858354—
ProductN-(5-bromo-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamideHCID 5336335482%

Reaction Steps

Using an analogous method to that described in Example 11, 3-amino-5-bromo-2-chloropyridine was reacted with and 4-fluorobenzenesulfonyl chloride to give N-(5-bromo-2-chloropyridin-3-yl)-4-fluorobenzenesulfonamide in 82% yield; 1H NMR Spectrum: (CDCl3) 8.21 (1H, d); 8.15 (1H, d); 7.84 (2H, m); 7.20 (2H, m); 6.97 (1H, br s); Mass Spectrum: M+H+ 365.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-f2a4cd7fb9004fb98099d865f5ea9dbe
Source noteuspto-grants-2011_01