摘要

A simple and highly efficient copper iodide catalyzed one-pot synthesis of 2-substituted quinazolin-4 (3H)-ones have been developed from anthranilamide, terminal alkynes and azides. A wide variety of alkynes were screened to understand the scope of this methodology. This method has been extended for the synthesis of 5-substituted pyrazolo[4,3-d]pyrimidin-7(6H)-ones which are having potential applications in medicinal chemistry.

  • 出版日期2017-7-26