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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340374Generated: October 25, 2026

3,5-Dichloro-2-cyanopyridine → HCID 66874911, compound

https://huagongshe.com/reaction/340374

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—
ProductHCID 66874911HCID 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 bi-carbonate 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 vacuo. 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 numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-ab267806ac65428e94eaa7d533628a16
Source noteuspto-grants-2014_11