首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of Dibenzo[f,h][1,2,4]triazolo[3,4-b]quinazolines via a Two-Step Route with Water as the Only By-Product
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Synthesis of Dibenzo[f,h][1,2,4]triazolo[3,4-b]quinazolines via a Two-Step Route with Water as the Only By-Product

机译:通过两步途径与水作为唯一副产物的两步途径合成二苯并[F,H] [3,4-B]喹唑啉

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摘要

Microwave-promoted cyclocondensation of isoflavones with 3-amino[1,2,4]triazole gave 6-phenyl-7-(2-hydroxyphenyl)-1,2,4triazolo-[4,3-a]pyrimidines as intermediates. Subsequent photocyclization of these intermediates delivered dibenzo[f,h][1,2,4] triazolo[3,4b] quinazolines as final products. Water was the only by-product in this two-step procedure. The products showed distinct fluorescence properties both in solution and in the solid state.
机译:微波促进异黄酮与3-氨基[1,2,4]三唑的异黄酮的环官致粘附,得到6-苯基-7-(2-羟基苯基)-1,2,4-9-1- [4,3-a]嘧啶作为中间体。 随后将这些中间体的光循环递送二苯并[F,H] [1,2,4]三唑[3,4b]喹唑啉作为最终产物。 水是这两步手术中唯一的副产品。 该产品在溶液和固态中显示出明显的荧光性能。

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