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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425605Generated: November 4, 2026

Sodium Carbonate → HCID 86674222, compound

https://huagongshe.com/reaction/1425605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Fluoropyridine-5-boronic acid pinacol esterHCID 12177222—
ReactantHCID 86674221HCID 86674221—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductHCID 86674222HCID 8667422267.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromo-2-(4-(methoxymethoxy)phenyl)-3-nitropyridine (68 mg, 0.2 mmol), 2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (45 mg, 0.2 mg), tetrakis(triphenylphosphine)palladium (12 mg, 0.01 mmol), Na2CO3 (0.5 mL, 1 M aqueous solution) and dioxane (1.5 mL) was heated at 100° C. for 10 min in a microwave reactor. After cooling to rt, the reaction was diluted with EtOAc (20 mL) and washed with brine (20 mL) and water (2×20 mL) and dried over MgSO4. Solvent was removed under reduced pressure and the residue was purified by silica chromatography (EtOAc in hexane, 5% to 40%) to afford 6′-fluoro-6-(4-(methoxymethoxy)phenyl)-5-nitro-3,3′-bipyridine as a yellow solid (48 mg, 67%). MS (ESI) m/z [M+H]+356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08932557B2
Source datasetuspto-grants-2015_01
ORD IDord-8d70c2d2891547fb83f2a6471f86f5d8
Source noteuspto-grants-2015_01