CuI/l-Proline-Catalyzed Intramolecular Aryl Amination: An Efficient Route for the Synthesis of 1,4-Benzodiazepinones
作者:K. Majumdar、Sintu Ganai
DOI:10.1055/s-0030-1260975
日期:2011.8
An effective protocol for the synthesis of potentially bio- active benzo(e)chromeno(6,5-b)(1,4)diazepine-3,8(7H,13H)-dione and dibenzo(b,e)(1,4)diazepin-11(10H)-one derivatives in good to excellent yields has been achieved by CuI/L-Proline catalyzed cou- pling reaction as the key step. The methodology offers clean reac- tion conditions and easy isolation of the products in 61-92% yields.
合成具有潜在生物活性的苯并 (e)chromeno(6,5-b)(1,4)diazepine-3,8(7H,13H)-dione 和 dibenzo(b,e)(1, 4)以CuI/L-脯氨酸催化偶联反应为关键步骤,获得了产率良好至优异的diazepin-11(10H)-one衍生物。该方法提供了清洁的反应条件和易于分离的产物,产率为 61-92%。