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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662536Generated: October 30, 2026

Potassium Carbonate → Dimethyl 4-(5-fluoro-2-(methyloxy)-4-pyridinyl)-1,3-benzenedicarboxylate

https://huagongshe.com/reaction/1662536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-[[(Trifluoromethyl)sulfonyl]oxy]-1,3-benzenedicarboxylic acid dimethyl esterHCID 12017546—
Reactant(5-Fluoro-2-methoxypyridin-4-yl)boronic acidHCID 44754837—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductDimethyl 4-(5-fluoro-2-(methyloxy)-4-pyridinyl)-1,3-benzenedicarboxylateHCID 5770606892.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 66.13B (1.00 g, 2.9 mmol) in DMF (12 mL) at 23° C. was added 5-fluoro-2-methoxypyridin-4-ylboronic acid (0.75 g, 4.4 mmol) (commercially available from Asymchem), potassium carbonate (1.2 g, 8.8 mmol), followed by tetrakis(triphenylphosphine)palladium (0.24 g, 0.20 mmol). The mixture was heated to 90° C. The reaction mixture was then stirred for 17 hours and then cooled to room temperature. The reaction was diluted with brine and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was then purified on silica gel (0-30% EtOAc in hexanes) to yield 83.21A as a colorless solid (0.860 g, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-336f2d4290f44b75abb6eb23a549e261
Source noteuspto-grants-2011_10