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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69146Generated: October 29, 2026

Tributylvinyltin → 5-Ethenyl-4-fluoropyridin-2-amine

https://huagongshe.com/reaction/69146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant5-Bromo-4-fluoropyridin-2-amine hydrochlorideHCID 71627067—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product5-Ethenyl-4-fluoropyridin-2-amineHCID 55283842—

Reaction Conditions

Temperature120 °C

Reaction Steps

5-Bromo-4-fluoro-pyridin-2-ylamine mono HCl salt (xvii) (368 mg, 1.62 mmol), tributyl(vinyl)stannane (0.52 mL, 1.78 mmol) and palladium tetrakis(triphenylphosphine) (19 mg, 0.016 mmol) in dioxane (6 mL) under argon were heated under microwave irradiation at 120° C. for 45 min. Were then added tributyl(vinyl)stannane (0.2 mL, 0.685 mmol) and palladium tetrakis(triphenylphosphine) (7 mg, 0.006 mmol) and the RM was placed under argon and heated once more under microwave irradiation at 120° C. for 45 min. The RM was diluted with EtOAc and washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by chromatography with hexane and EtOAc to yield the title product as a yellow solid (tR 1.76 min (conditions 8), MH+=139).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-90a5a3ec9c8743f2b363a98f2d86c93a
Source noteuspto-grants-2014_09