Abstract
Present manuscript describes the synthesis and molecular structure features of novel condensed pyrido[1,2-a]quinazolines. The above-mentioned compounds were synthesized via condensation of 2-[azolyl-(аzinyl-)]anilines with 5-oxohexanoic acid. The tandem condensation intermediates were isolated and cyclized under various conditions. The structures of synthesized compounds were confirmed by LC-MS and NMR-spectroscopy. The existence of the substituted pyrido[1,2-a][1,2,4]triazolo[1,5-c]quinazolines molecules as superposition of two resonance structures was detected by the X-Ray analysis.
Graphical Abstract
Disclosure statement
No potential conflict of interest was reported by the author(s).