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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063250Generated: October 25, 2026

1-Ethynyl-4-fluorobenzene → 4-[2-(4-Fluorophenyl)ethynyl]-2-(methylthio)pyrimidine

https://huagongshe.com/reaction/2063250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
Reactant4-Iodo-2-(methylthio)pyrimidineHCID 3858901—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product4-[2-(4-Fluorophenyl)ethynyl]-2-(methylthio)pyrimidineHCID 2267524352.8%

Reaction Steps

4-Iodo-2-(methylthio)pyrimidine (35.7 g, 142 mmol) and 1-ethynyl-4-fluorobenzene (17.0 g, 142 mmol) were added to triethylamine (200 mL) at room temperature. To the resulting solution were added dichlorobis(triphenylphosphine)palladium(II) (1.0 g, 1.4 mmol) and copper iodide (1.0 g, 5.2 mmol). Then the reaction mixture was stirred under a nitrogen atmosphere at room temperature for 18 h. The reaction mixture was concentrated under reduced pressure to remove excess triethylamine. The residue was partitioned between water (400 mL) and dichloromethane (400 mL). The organic layer was washed with water (2×400 mL) and dried (MgSO4), and the solvent was evaporated under reduced pressure to give an oil. Flash chromatographic purification on silica gel with 0 to 50% ethyl acetate/hexanes as eluant gave 18.3 g of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288375B2
Source datasetuspto-grants-2012_10
ORD IDord-154121dcf388495b8141c48fbf696cbd
Source noteuspto-grants-2012_10