Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056893Generated: October 25, 2026

Dimethyl Sulfoxide → 3'-fluoro-4'-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2'-bipyridin-4-one

https://huagongshe.com/reaction/1056893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DIFLUORO-4-IODOPYRIDINEHCID 11447837—
Reactant3-[(4-methoxybenzyl)oxy]pyridin-4(1H)-oneHCID 67405695—
SolventEthyl AcetateHCID 8857—
Product3'-fluoro-4'-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2'-bipyridin-4-oneHCID 67418473—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a 20 mL microwave vial (Biotage) was added 0.70 g (3.03 mmol) 3-[(4-methoxybenzyl)oxy]pyridin-4(1H)-one, 1.26 g (9.08 mmol) potassium carbonate, 1.10 g (4.54 mmol) 2,3-difluoro-4-iodopyridine and 15 mL DMSO, A yellow suspension formed and the vial was sealed and heated at 85° C. for 48 h on a heat block. The suspension was cooled, diluted with ethyl acetate, and washed twice with 10 mL brine. The organic layer was dried over sodium sulfate, filtered, and evaporated onto silica gel. Purification by flash chromatography (silica gel 0-100% hexanes/EtOAc gradient, followed by 10% MeOH in EtOAc) afforded 3′-fluoro-4′-iodo-3-[(4-methoxybenzyl)oxy]-4H-1,2′-bipyridin-4-one as a yellow solid. LCMS (M+H)+ 453.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399651B2
Source datasetuspto-grants-2016_07
ORD IDord-fddb9030d44b4f3a9472ed4e70b53494
Source noteuspto-grants-2016_07