Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646227Generated: October 26, 2026

3-(3-Ethynylphenyl)-2-fluoropyridine → 2-fluoro-3-(3-{[1-(2-fluoroethyl)-1H-pyrazol-4-yl]ethynyl}phenyl)pyridine

https://huagongshe.com/reaction/646227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Ethynylphenyl)-2-fluoropyridineHCID 59772650—
Reactant1-(2-fluoroethyl)-4-iodo-1H-pyrazoleHCID 59772706—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product2-fluoro-3-(3-{[1-(2-fluoroethyl)-1H-pyrazol-4-yl]ethynyl}phenyl)pyridineHCID 5977265976%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 1-(2-fluoroethyl)-4-iodo-1H-pyrazole (148 mg, 0.62 mmol) in DMF (5.0 mL) is added dichlorobis(triphenylphosphine)palladium (16 mg, 0.022 mmol), copper iodide (3 mg, 0.015 mmol), TEA (0.53 mL, 3.8 mmol) and 3-(3-ethynylphenyl)-2-fluoropyridine (150 mg, 0.76 mmol). The reaction mixture is heated at 65° C. for 3 h, cooled and quenched with H2O. The aqueous layer is extracted with EtOAc. The combined organic extracts are washed with brine, dried (MgSO4) and concentrated. The crude material is purified by chromatography (silica gel, EtOAc/hexane:30/70) to afford the title compound (145 mg, 76%) as an oil. MS (+) ES: 310 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705030B2
Source datasetuspto-grants-2010_04
ORD IDord-a8bf72ace6474d46b26ca3fccc5552c7
Source noteuspto-grants-2010_04