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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716280Generated: October 31, 2026

Pyridine → 4-(4-Chloro-phenoxy)-N-(2,5-dibromo-pyridin-3-yl)-benzenesulfonamide

https://huagongshe.com/reaction/1716280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(4-Chlorophenoxy)benzene-1-sulfonyl chlorideHCID 2757750—
Reactant2,5-Dibromopyridin-3-amineHCID 19387532—
SolventDichloromethaneHCID 6344—
Product4-(4-Chloro-phenoxy)-N-(2,5-dibromo-pyridin-3-yl)-benzenesulfonamideHCID 86619933—

Reaction Steps

To a solution of 2,5-dibromo-3-aminopyridine (0.51 g, 2.0 mmol) and 4-(4-chloro-phenoxy)-benzenesulfonyl chloride (0.76 g, 2.0 mmol) in dry CH2Cl2 (10 mL) was added pyridine (1 mL) at 0 C. The resulting mixture was allowed to warm to room temperature and stirred until TCL showed the completion of the reaction. The reaction mixture was diluted with CH2Cl2 and washed with aqueous HCl solution. After the pyridine was neutralized, the organics were washed with water, brine and dried over anhydrous Na2SO4. The filtration (Celite) and concentration under vacuo gave a crude material, which was purified by silica column (30% EtOAc/hexanes). MS: 516, 518 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-d44ecc8be2504abf90045b8b7f55bda9
Source noteuspto-grants-2010_09