SYNTHESIS OF TETRAZOLE DERIVATIVES THROUGH CONVERSION OF AMIDE AND THIOAMIDE FUNCTIONALITIES
DOI:
https://doi.org/10.1007/6397Ключевые слова:
amide, 1, 5-disubstituted tetrazole, thioamide, bioisosterism, drug design, isostereАннотация
The chemical and physiological stability of tetrazole motifs, as well as their broad range of medicinal properties, have been intensively investigated. But still, scientific community uses the best efforts to develop structurally different variations of substituted tetrazoles to investigate their potential applications. In this review, various methods applying combinations of different reagents such as SiCl4/NaN3, PCl5/N2H4/N2O4, PPh3/DEAD/TMSN3, NaN3/HgCl2, and DPPA/DIAD for the selective synthesis of 1,5-disubstituted tetrazoles converting amide and thioamide functionalities have been described. This approach of thioamide and amide replacement allows to introduce tetrazole as isosteric substituent increasing metabolic stability of biologically active compounds.