A simple and efficient protocol for the synthesis of 5-aryl-2-(2-substituted-1,8-naphthyridin-3-yl)-thiazolo[3,2-b][1,2,4]triazoles (4) is achieved by cyclocondensation of 3-(2-substituted-1,8-naphthyridin-3-yl)-1,2,4-triazoles (3) with α-halogenoketones in anhyd. methanol under microwave irradiation. The products are obtained in good yields and in a state of high purity.
一种简单而有效的合成5-芳基-2-(2-取代的1,8-萘啶-3-基)-噻唑并[3,2- b ] [1,2,4]三唑的方案(4)通过将3-(2-取代的1,8-萘啶-3-基)-1,2,4-三唑(3)与α-卤代酮在酸酐中进行环缩合可实现。微波辐射下的甲醇。以高收率和高纯度获得产物。