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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634898Generated: October 30, 2026

Ethyl 2-chloroisonicotinate → Ethyl 2-(3,4,5-trimethoxyphenylethynyl)pyridine-4-carboxylate

https://huagongshe.com/reaction/1634898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroisonicotinateHCID 2762942—
Reactant5-Ethynyl-1,2,3-trimethoxybenzeneHCID 11830260—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(3,4,5-trimethoxyphenylethynyl)pyridine-4-carboxylateHCID 18674974—

Reaction Conditions

Temperature45 °C

Reaction Steps

3,4,5-Trimethoxyphenylacetylene (1.80 g), ethyl 2-chloroisonicotinate (2.08 g) and copper iodide (71 mg) were dissolved in a mixed solvent of DMF (4 mL) and triethylamine (8 mL), and to the solution bis-(triphenylphosphine)palladium dichloride (0) (131 mg) was added, and the mixture was stirred at 45° C. for 4 hours under an argon atmosphere. The reaction mixture was diluted with ethyl acetate, washed with 2 M hydrochloric acid, water and saturated brine, dried over anhydrous sodium sulfate. After concentrating the reaction mixture under reduced pressure, the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=4:1 to 3:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509329B1
Source datasetuspto-grants-2003_01
ORD IDord-3d540c9f63c94badba83729f06af6a5a
Source noteuspto-grants-2003_01