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首页> 外文期刊>Archiv der Pharmazie >Pyrido (2, 3-d)pyrimidines and Pyrimido(5', 4':5, 6)pyrido(2, 3-d)pyrimidines as New Antiviral Agents: Synthesis and Biological Activity.
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Pyrido (2, 3-d)pyrimidines and Pyrimido(5', 4':5, 6)pyrido(2, 3-d)pyrimidines as New Antiviral Agents: Synthesis and Biological Activity.

机译:作为新的抗病毒剂的嘧啶(2,3-d)嘧啶和嘧啶(5',4':5,6)吡啶(2,3-d)嘧啶:合成和生物活性。

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摘要

A series of 7-amino- and 7-oxo-5-aryl-6-cyanopyrido[2, 3-d]pyrimidines, 4 and 11, respectively, and pyrimido [5', 4':5, 6]pyrido[2, 3-d]pyrimidine derivatives 6 and 7 was synthesized and investigated as antiviral agents. Different synthetic strategies for the preparation of the target compounds were explored. A synthetic procedure for 4 and 11 starting with 6-amino-1, 2, 3, 4-tetrahydro-2, 4-dioxopyrimidine, proper aldehyde, and malononitrile or ethyl cyanoacetate, respectively, in a one-pot reaction proved to be the method of choice for preparation of compounds of such type. Construction of another pyrimidine ring on the pyridine nucleus of compound 4 was achieved either by reaction with phenyl iso(thio)cyanate or with formic acid to yield 6 and 7, respectively. The structure of the prepared compounds was confirmed through elemental analysis and spectral investigation. Most of the newly synthesized compounds were subjected to antiviral activity testing against herpes simplex virus (HSV) where some of them show good activities.
机译:分别由一系列的7-氨基-和7-氧代-5-芳基-6-氰基吡啶[2,3-d]嘧啶和嘧啶基[5',4':5,6]吡啶[2]合成3-d]嘧啶衍生物6和7,并将其作为抗病毒剂进行研究。探索了用于制备目标化合物的不同合成策略。通过一锅反应,分别以6-氨基-1、2、3、4-四氢-2、4-二氧代嘧啶,适当的醛和丙二腈或氰基乙酸乙酯为原料,合成4和11的合成方法是制备此类化合物的选择方法。通过与异(硫)氰酸苯基酯或与甲酸反应分别得到6和7,可在化合物4的吡啶核上构建另一个嘧啶环。通过元素分析和光谱研究证实了所制备化合物的结构。大多数新合成的化合物都经过了针对单纯疱疹病毒(HSV)的抗病毒活性测试,其中一些化合物表现出良好的活性。

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