Table 2. Synthesis of 3-Substituted Quinazoline-2,4-diones 6a–pa.
All reactions were conducted using 2a–p (1 mmol, 1.0 equiv), (Boc)2O (1.5 mmol, 1.5 equiv), DMAP (0.1 mmol, 0.1 equiv), isolated yield.
The reaction was run in 3 mL of CH3CN under the MW condition for 30 min.
The reaction was run in 10 mL of CH3CN at room temperature for 12 h.