Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499582Generated: November 1, 2026

Diisopropylethylamine → Methyl 6-(2,6-difluoro-4-(methoxymethyl)phenyl)-5-fluoropicolinate

https://huagongshe.com/reaction/1499582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-bromo-5-fluoropyridine-2-carboxylateHCID 46311204—
Reactant2-[2,6-Difluoro-4-(methoxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 86726804—
CatalystHCID 178418851HCID 178418851—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 6-(2,6-difluoro-4-(methoxymethyl)phenyl)-5-fluoropicolinateHCID 70655699—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-[2,6-difluoro-4-(methoxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.364 g, 1.28 mmol), methyl 6-bromo-5-fluoropyridine-2-carboxylate (0.300 g, 1.28 mmol) and DIPEA (0.67 mL, 3.8 mmol) in 1,4-dioxane (6 mL) and water (0.30 mL) was purged with nitrogen. Bis(tri-tert-butylphosphine)palladium (65.5 mg, 0.128 mmol) was added to the mixture. The resulting reaction mixture was then heated at 120° C. for 40 min. The mixture was filtered through a pad of diatomaceous earth and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluting with 0-50% EtOAc in hexanes) to give methyl 6-[2,6-difluoro-4-(methoxymethyl)phenyl]-5-fluoropyridine-2-carboxylate as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-4f8a6614276f4955b841679e7108227b
Source noteuspto-grants-2015_12