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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499551Generated: November 2, 2026

1,4-Dioxane → Methyl 6-(2,6-difluoro-4-(methylthio)phenyl)-5-fluoropicolinate

https://huagongshe.com/reaction/1499551

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-bromo-5-fluoropyridine-2-carboxylateHCID 46311204—
Reactant2-(2,6-Difluoro-4-(methylthio)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 66652494—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
ProductMethyl 6-(2,6-difluoro-4-(methylthio)phenyl)-5-fluoropicolinateHCID 6665247740.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a sealed tube, a mixture of 2-[2,6-difluoro-4-(methylthio)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.00 g, 3.49 mmol), methyl 6-bromo-5-fluoropyridine-2-carboxylate (1.23 g, 5.24 mmol) and DIPEA (1.83 mL, 10.5 mmol) in a mixed solvent of 1,4-dioxane (15 mL) and water (0.51 mL) was stirred and flushed with nitrogen bubbles for 5 min. before bis(tri-tert-butylphosphine)palladium (360 mg, 0.70 mmol) was added. The reaction mixture was heated at 120° C. for 30 min. After cooling, the reaction mixture was filtered, and the filter was washed with THF. The filtrate was concentrated and then purified by silica gel column chromatography using CombiFlash® (0 to 20% EtOAc in hexanes) to give the sub-title compound as powder (442 mg, 40%). LCMS calc. for C14H11F3NO2S (M+H)+: m/z=314.1. Found: 314.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-536c063def5a4555ae4a97bea276df49
Source noteuspto-grants-2015_12