Catalytic role of Cu(I) species in Cu2O/CuI supported on MWCNTs in the oxidative amidation of aryl aldehydes with 2-aminopyridines

Cu2O and CuI were supported on multiwalled carbon nanotubes (MWCNTs) using a wet impregnation method, and the resulting materials were fully characterized by powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy, transmission electron microscopy, and temperature-programmed desorption with ammonia analysis. The results of these experiments revealed that Cu2O and CuI were deposited on the MWCNTs in the cubic and γ phases, respectively. These results also showed that the Cu-containing MWCNTs exhibited weak to strong electron-accepting (Lewis acidic) properties. The catalytic activities of these materials were studied for the synthesis of biologically significant N-(pyridin-2-yl)benzamides via the oxidative amidation of aryl aldehydes with 2-aminopyridines. The yields of the products were in the range 50%–95% with 100% selectivity. Notably, the CuI/MWCNT catalyst was much more effective than the Cu2O/MWCNT catalyst with respect to the isolated yield of the product, although the latter of these two catalysts exhibited much better recyclability. A preferential interaction was observed between the polar nature of the acid-activated MWCNTs and the ionic Cu2O compared with covalent CuI. The differences in these interactions had a significant impact on the rate of the nucleophilic attack of the amino group of 2-aminopyridine substrate on the carbonyl group of the aryl aldehyde.

Graphical AbstractSeveral composite Cu(I) species supported on MWCNTs have been synthesized using a wet impregnation method. Characterization revealed the formation of cubic phase Cu2O and γ-phase CuI on the MWCNTs. The 20% Cu2O/MWCNT and 20% CuI/MWCNT catalysts were efficient for the synthesis of N-(pyridin-2-yl)benzamides under mild reaction conditions with 100% selectivity and good yields.Figure optionsDownload as PowerPoint slide