Abstract:
New dihydropyrano[4,3-d]pyrimidines bearing 7-positioned spiro-linked azacycloalkane moieties were obtained by the Prins spirocyclization of commercially available N-protected azacycloalkanones followed by the regiospecific condensation with dimethylformamide dimethyl acetal and amidines. The new scaffold thus accessed appears to be a valuable building block for drug development.
Keywords:spiro compounds, pyrimidine synthesis, pyrano[4,3-d]pyrimidine, regiospecificity, drug design.