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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >A DIVERSIFIED APPROACH TO THE SYNTHESIS OF HIGHLY FUNCTIONALIZED NOVEL AZINES AND AZOLES FROM 2H-PYRAN-2-ONES
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A DIVERSIFIED APPROACH TO THE SYNTHESIS OF HIGHLY FUNCTIONALIZED NOVEL AZINES AND AZOLES FROM 2H-PYRAN-2-ONES

机译:从2H-PYRAN-2-ONE合成高功能新型偶氮和偶氮的多样化方法

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摘要

One-pot regioselective synthesis of 2,6-diarylpyrimidines (4), 2,6-disubstituted pyridines (5 and 6), 5-aryl-3-cyanomethyl-1H-pyrazoles (7) through base catalyzed ring transformation of suitably functionalized 2H-pyran-2-ones by arylamidines, cyanamide, ammonium carbonate, hydrazines respectively has been developed. Our synthetic approach opened a new avenue for the regioselective synthesis of 2,6-diarylpyrimidines and 2,6-disubstituted pyridines and cyanomethylpyrazoles. The procedure is very simple, efficient and economically viable. The protocol provides an efficient methodology for the preparation of new class of medicinally useful and highly functionalized azines and azoles from single precursor 2H-pyran-2-ones.
机译:通过适当官能化的2H的碱催化环转化,一锅区域选择性地合成2,6-二芳基嘧啶(4),2,6-二取代吡啶(5和6),5-芳基-3-氰基甲基-1H-吡唑(7)已开发出分别由芳基嘧啶,氰胺,碳酸铵,肼形成的-吡喃-2-酮。我们的合成方法为2,6-二芳基嘧啶,2,6-二取代的吡啶和氰基甲基吡唑的区域选择性合成开辟了新途径。该过程非常简单,有效并且在经济上可行。该协议为从单一前体2H-吡喃-2-酮制备新型医学上有用的且高度官能化的嗪类和唑类提供了一种有效的方法。

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