Pyrazoles containing amino and carbonitrile groups have a wide range of biological activities, including antimicrobial, antiinflammatory, antitumor, antioxidant, and are used to create pesticides and dyes. Also, these compounds are synthons for the preparation of various polyheterocyclic compounds. New potentially biologically active 5-amino-3-aryl-1H-pyrazole-4-carbonitriles containing pharmacophoric substituents have been obtained via three-component condensation reactions of malonic dinitrile with substituted aromatic aldehydes and benzhydrazides or hydrazines.
In the course of this work, fl uorinated catalysts MoO3 /Al2 O3 -F for the olefi ns metathesis have been synthesized. The materials have been characterized by various physicochemical methods and tested in the propylene metathesis reaction. It has been shown that the support fl uorination leads to partial replacement of surface hydroxyl groups by F, which is accompanied by an increase in the strength of both Lewis acid sites and residual bridging OH groups. Increasing the fl uorine content on γ-Al2O3 up to 3 wt.
Condensation of 2-aminobenzimidazole, ortho-substituted benzaldehydes and cyclohexanone proceeds with the formation of 10-o-Rsubstituted phenyl benz[4,5]imidazolo-6,7,8,9,10,11-hexahydro[1,2-a] quinazolines having angular articulation rings, strukture which is set using IR, NMR, 1 H, 13C spectra.
