Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259194Generated: October 27, 2026

Triethylamine → N-(4-((5-chloro-6-cyanopyridin-3-yl)ethynyl)phenyl)acetamide

https://huagongshe.com/reaction/1259194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dichloro-2-cyanopyridineHCID 2769699—
ReactantN-(4-ethynylphenyl)acetamideHCID 11412536—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(4-((5-chloro-6-cyanopyridin-3-yl)ethynyl)phenyl)acetamideHCID 66875230—

Reaction Steps

A solution of 3,5-dichloropicolinonitrile (1.0 eq.), N-(4-ethynylphenyl)acetamide (from the previous step) (1.0 eq.), bis(triphenyl-phosphine)palladium chloride (10 mol %), copper iodide (10 mol %), and triethylamine (5.0 eq.) in DMF (0.04 M) was stirred at 60° C. for 4 hours. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and water. The two phases were separated. The organic layer was washed twice with water, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give N-(4-((5-chloro-6-cyanopyridin-3-yl)ethynyl)phenyl)acetamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-7b3a1e8c42d44b67888a3bafa8f05cc6
Source noteuspto-grants-2013_06