Abstract
A mild, green, and facile route to the synthesis of 3,4,4a,5‐tetrahydro‐4a‐methyl‐2H‐pyrido[1,2‐a]quinazoline‐1,6‐dione derivatives has been developed. In the presence of iodine, a variety of 2‐aminobenzamides underwent a tandem reaction with 6‐chlorohexan‐2‐one to afford the corresponding pyridoquinazolines in good to high yields.
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