An efficient catalysis for the synthesis of pyrimido[1,2-]benzimidazoles and 1-(benzothiazolylamino)methyl-2-naphthols using ZnO@SOH@Tropine

In this research and in the line of our researches on the use of nano-substrates modified with ionic liquid in organic reactions, an efficient and green method for the one-pot three-component synthesis of pyrimido[1,2- a ]benzimidazole and 1-(benzothiazolylamino)methyl-2-naphthol derivatives is reported using a new nanoporous catalyst formulated as ZnO@SO 3 H@Tropine. Further analysis of the catalyst for its characterization has been performed using thermal gravimetric analysis (TGA), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), energy dispersive spectrometer (EDS) and Fourier-transform infrared spectroscopy (FT-IR). The present approach creates a variety of biologically active heterocyclic compounds with excellent yields and short reaction times. Among the other advantages of the current method are: ease of operation, clean reaction profiles and ease of separation. Also, this catalyst can be reused five times without loss of its catalytic activity. An efficient, green method for one-pot three-component synthesis of pyrimido[1,2- a ]benzimidazole and 1-(benzothiazolylamino)methyl-2-naphthol derivatives using a new nanoporous catalyst ZnO@SO 3 H@Tropine is reported. Advantages include, but are not limited to, simple work-up and high yields.