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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048016Generated: October 30, 2026

Potassium Carbonate → N-(sec-butylsulfonyl)-4-[(5-chloro-6-methoxypyridin-3-yl)oxy]-2,5-difluorobenzamide

https://huagongshe.com/reaction/2048016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(sec-butylsulfonyl)-2,4,5-trifluorobenzamideHCID 58042392—
Reactant3-Chloro-5-hydroxy-2-methoxypyridineHCID 66667383—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-(sec-butylsulfonyl)-4-[(5-chloro-6-methoxypyridin-3-yl)oxy]-2,5-difluorobenzamideHCID 5804238452.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

Potassium carbonate (0.140 g, 1.01 mmol) was added to a stirred solution of N-(sec-butylsulfonyl)-2,4,5-trifluorobenzamide (Preparation 68, 0.090 g, 0.30 mmol) in DMSO (1 mL). After 10 minutes a solution of 5-chloro-6-methoxypyridin-3-ol (Preparation 77, 0.088 g, 0.51 mmol) in DMSO (2 mL) was added at room temperature. The mixture was heated at 90° C. for 72 hours. The reaction mixture was diluted with water (25 mL) and extracted with EtOAc (3×25 mL). The combined organics were washed with water (25 mL), dried over magnesium sulfate, filtered, evaporated in vacuo. The resulting crude product was purified by silica gel chromatography eluting with 0 to 66% EtOAc in heptane to yield the title compound (0.068 g):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592629B2
Source datasetuspto-grants-2013_11
ORD IDord-86492491a40b49ce90fd01bffc4fd302
Source noteuspto-grants-2013_11