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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178112Generated: October 25, 2026

3-Chloro-2-fluoro-5-hydroxypyridine → 4-[(5-chloro-6-fluoropyridin-3-yl)oxy]-3-cyano-N-(5-fluoropyridin-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/2178112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-fluoro-5-hydroxypyridineHCID 22451555—
Reactant3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamideHCID 59436600—
Product4-[(5-chloro-6-fluoropyridin-3-yl)oxy]-3-cyano-N-(5-fluoropyridin-2-yl)benzenesulfonamideHCID 117653188—

Reaction Steps

The title compound was prepared according to the method described for Method Variation 1 using 3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide (Preparation 2) and 3-chloro-2-fluoro-5-hydroxypyridine and then purified using silica gel column chromatography eluting with 30-35% EtOAc in heptanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067922B2
Source datasetuspto-grants-2015_06
ORD IDord-5e427315feae431dbc92cb1f7437f91f
Source noteuspto-grants-2015_06