Abstract
An efficient one‐pot synthesis of 2‐aryl‐4(3H)‐quinazolinones from 2‐amino benzamides and substituted benzoyl chlorides in a room temperature ionic liquid is described. Compared with the classical reaction conditions, this new synthetic method has the advantages of recyclability of ionic liquid, very good to excellent yields (78–92%), the absence of hazardous and expensive catalysts, and easy workup procedures giving rise to a process with minimum waste.
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