Abstract
A novel and efficient carbodiimide-mediated synthetic method for new 2,3-dihydro-6 H-pyrimido[2,1- b]quinazolin-4(1 H)-ones ( 4) is described which involves initial intramolecular addition of an amino-nucleophile to the carbodiimide-cumulenic system, followed by intramolecular hetero conjugate addition annulation.
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