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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048095Generated: November 1, 2026

Potassium Carbonate → 4-methylphenyl 5-chloro-4-({5-chloro-6-[(1S)-2,2,2-trifluoro-1-methylethoxy]pyridin-3-yl}oxy)-2-fluorobenzoate

https://huagongshe.com/reaction/2048095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-chloro-6-[(1S)-2,2,2-trifluoro-1-methylethoxy]pyridin-3-olHCID 58042457—
ReactantHCID 58042518HCID 58042518—
SolventDimethyl SulfoxideHCID 679—
Product4-methylphenyl 5-chloro-4-({5-chloro-6-[(1S)-2,2,2-trifluoro-1-methylethoxy]pyridin-3-yl}oxy)-2-fluorobenzoateHCID 5804250886%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 5-chloro-6-[(1S)-2,2,2-trifluoro-1-methylethoxy]pyridin-3-ol (Preparation 231, 60 mg, 0.25 mmol) and 4-methylphenyl 5-chloro-2,4-difluorobenzoate (Preparation 26, 70 mg, 0.25 mmol) in DMSO (1 mL) was added K2CO3 (69 mg, 0.50 mmol) at room temperature under N2 and the resulting mixture was stirred for 4 hours. The reaction mixture was warmed up to 50° C. and stirred for 1 hour before cooling to room temperature and stirring for 18 hours. The reaction was quenched with water and partitioned between water and DCM (3×5 mL). The mixture was filtered through a phase separation cartridge, the organic phase was washed with brine (3 mL) and filtered through another phase separation cartridge. The filtrate was dried by N2 blowing to give a crude product that was purified by silica gel column chromatography eluting with 0-20% EtOAc in heptane to give the title compound (108 mg, 86%) as colourless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592629B2
Source datasetuspto-grants-2013_11
ORD IDord-a23c49f04771439aaea773e56d122fe5
Source noteuspto-grants-2013_11