摘要
A novel and straightforward method for the synthesis of quinazolin-4(3H)-ones is described. The one-pot reaction between isatoic anhydride and (het)arylmethanamines led to the formation of N-substituted anthranilamides, which under aerobic conditions in the presence of CuBr undergo an in situ oxidation-cyclization reaction to produce quinazolin-4(3H)-ones in good yields.
- 出版日期2016-8-17