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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479660Generated: October 30, 2026

3,5-Dichloro-2-cyanopyridine → 5-((4-Acetylphenyl)ethynyl)-3-chloropicolinonitrile

https://huagongshe.com/reaction/1479660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
Reactant1-(4-Ethynylphenyl)ethan-1-oneHCID 5123626—
Reactanttriethylamine N,N-dimethylformamideHCID 22056947—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product5-((4-Acetylphenyl)ethynyl)-3-chloropicolinonitrileHCID 66874911—

Reaction Steps

To a solution of 1-(4-ethynylphenyl)ethanone (commercially available) (1 eq) 3,5-dichloropicolinonitrile (1 eq), dichlorobis(triphenylphosphine)-palladium (II) (20 mol %), copper iodide (10 mol %) and DMF:Triethylamine (10:1) (0.13 M) was stirred at ambient temperature overnight. The reaction mixture was then diluted with ethyl acetate and sodium bicarbonate solution. The two phases were separated, and the aqueous phase was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane and 5-((4-acetylphenyl)ethynyl)-3-chloropicolinonitrile was isolated as a yellow solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-1dce481e0e9f462ca13427305d945274
Source noteuspto-grants-2016_08