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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512025Generated: November 2, 2026

Potassium Carbonate → 4-({[5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-yl]oxy}methyl)-2,5-difluoro-N-(methylsulfonyl)benzamide

https://huagongshe.com/reaction/512025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-olHCID 66666942—
Reactant4-(Bromomethyl)-2,5-difluoro-N-(methylsulfonyl)benzamideHCID 66667111—
SolventHydrochloric AcidHCID 313—
SolventDimethyl SulfoxideHCID 679—
Product4-({[5-Chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-yl]oxy}methyl)-2,5-difluoro-N-(methylsulfonyl)benzamideHCID 8668256678.6%

Reaction Steps

Potassium carbonate (61 mg, 0.229 mmol) was added to a solution of 5-chloro-6-(3,3,3-trifluoropropoxy)pyridin-3-ol (Preparation 67, 45 mg, 0.19 mmol) in DMSO (2 mL) and the reaction mixture was stirred under a nitrogen atmosphere at room temperature for 5 minutes. 4-(Bromomethyl)-2,5-difluoro-N-(methylsulfonyl)benzamide (Preparation 10, 63 mg, 0.19 mmol) was then added and the resulting mixture stirred under nitrogen at room temperature for 120 hours. The reaction mixture was diluted with aqueous hydrochloric acid solution (2 M, 15 mL), extracted with EtOAc (20 mL). The organic layer was washed with aqueous hydrochloric acid solution (2 M, 2×10 mL), dried over magnesium sulfate, filtered and evaporated in vacuo. The resulting crude solid was triturated with TBME/heptane (2:1), washed with heptane and dried in vacuo to yield the title compound as an off-white solid (73 mg, 74%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102621B2
Source datasetuspto-grants-2015_08
ORD IDord-3977a7a4b105426f955c028fdad0c22e
Source noteuspto-grants-2015_08