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首页> 外文期刊>Beilstein journal of organic chemistry. >Regioselective synthesis of 7,8-dihydroimidazo[5,1-c][1,2,4]triazine-3,6(2H,4H)-dione derivatives: A new drug-like heterocyclic scaffold
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Regioselective synthesis of 7,8-dihydroimidazo[5,1-c][1,2,4]triazine-3,6(2H,4H)-dione derivatives: A new drug-like heterocyclic scaffold

机译:区域选择性合成7,8-二氢咪唑并[5,1-c] [1,2,4]三嗪-3,6(2H,4H)-二酮衍生物:一种新型药物样杂环骨架

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摘要

Dihydroimidazo[5,1-c][1,2,4]triazine-3,6(2H,4H)-dione derivatives were prepared by successive N3- and N1-alkylation of hydantoins, followed by regioselective thionation and subsequent cyclization under mild conditions. In a final alkylation step a further substituent may be introduced. The synthetic strategy allows broad structural variation of this new drug-like heterobicyclic scaffold. In addition to extensive NMR and MS analyses, the structure of one derivative was confirmed by X-ray crystallography.
机译:二氢咪唑并[5,1-c] [1,2,4]三嗪-3,6(2H,4H)-二酮衍生物的制备方法是依次进行乙内酰脲的N3-和N1-烷基化,然后进行区域选择性硫磺化,然后在温和的条件下环化条件。在最终的烷基化步骤中,可以引入另外的取代基。合成策略允许这种新的药物样异双环支架的广泛结构变化。除了广泛的NMR和MS分析外,还通过X射线晶体学确定了一种衍生物的结构。

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