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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888564Generated: October 26, 2026

5-Bromo-2-fluoropyridine-3-boronic Acid (contains varying amounts of Anhydride) → 5-Bromo-2-fluoro-6'-methoxy-[3,4]bipyridinyl-3'-ylamine

https://huagongshe.com/reaction/1888564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-fluoropyridine-3-boronic Acid (contains varying amounts of Anhydride)HCID 2783242—
Reactant4-Iodo-6-methoxypyridin-3-amineHCID 11021287—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventPotassium FluorideHCID 522689—
Product5-Bromo-2-fluoro-6'-methoxy-[3,4]bipyridinyl-3'-ylamineHCID 5826651971%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 6-methoxy-4-iodopyridin-3-amine (9.5 g, 38 mmol), 5-bromo-2-fluoropyridin-3-ylboronic acid (16.7 g, 76 mmol), and 1,1′-[bis(diphenylphosphino)ferrocene] dichloropalladium(II) (1.5 g, 2 mmol) in 1N aqueous potassium fluoride (95 mL) and acetonitrile (200 mL) was heated at 95° C. for 16 h. The cooled reaction mixture was diluted with water (100 mL) and extracted with DCM (3×100 mL). The combined organic layer was dried over sodium sulfate, filtered, and evaporated to afford a residue which was purified by flash chromotagraphy (silica, 120 g column, ISCO, 0-40% ethyl acetate in hexanes) to afford the title compound as a yellow/orange solid (8.0 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-46f763e4584a4f65bec2e8ab894e4a0d
Source noteuspto-grants-2013_08