Efficient Method for the Synthesis of Novel Oxazinoquinolinones

Pyranoquinoline skeletons including both a quinoline ring and a pyran moiety afford exceptional biological activities.Rings annulated to the pyranoquinolinone units showed potential medicinal properties such as antibacterial anticoagulant antitumorand microtubule targeting agents. Despite the extensive body of published work on the synthesis of this type of compounds we are not aware of any report that describes a simple procedure for the annulation of an oxazole and /or oxazino nucleus to the pyranoquinolinone moiety to give a tetracyclic system. Oxazole and/ or oxazino derivatives have been found in numerous natural products and many of them have been shown to have an interesting broad range of biological activities such as in inhibition of Streptococcus mutans biofilm formationantipsychotics HIV inhibitory and anti-tumoral activities.