首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and Biological Activities of Some New Annulated Pyrazolopyranopyrimidines and Their Derivatives Containing Indole Nucleus
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Synthesis and Biological Activities of Some New Annulated Pyrazolopyranopyrimidines and Their Derivatives Containing Indole Nucleus

机译:某些新型的环式吡唑并吡喃并嘧啶及其吲哚核衍生物的合成及生物活性

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摘要

The key intermediate 6-amino-3-methyl-4-aryl-1-(5'-substituted-3'-phenyl-1H-indol-2'-carbonyl)- 1,4-dihydropyrano[2,3-c]pyrazol-5-carbonitriles 3a–o were prepared by cyclocondensation of 3-methyl-1-(5'-substituted-3'-phenyl-1H-indol-2'-carbonyl)-5-(4H)-pyrazolones 1a–c with arylidine derivatives of malononitrile 2a–e. The compounds 3a–o were subjected to cyclocondensation reaction with formamide, formic acid, and carbon disulfide to afford the title compounds 4a–o, 5a–o, and 6a–o, respectively. The structures of all these previously unknown compounds were confirmed by their spectral studies and elemental analysis. These compounds were screened for their antimicrobial and antioxidant activities.
机译:关键中间体6-氨基-3-甲基-4-芳基-1-(5'-取代的3'-苯基-1H-吲哚-2'-羰基)-1,4-二氢吡喃[2,3-c]吡唑-5-腈3a-o是通过3-甲基-1-(5'-取代-3'-苯基-1H-吲哚-2'-羰基)-5-(4H)-吡唑啉酮1a-c的环缩反应制备的与丙二腈2a–e的芳基衍生物。使化合物3a-o与甲酰胺,甲酸和二硫化碳进行环缩合反应,分别得到标题化合物4a-o,5a-o和6a-o。所有这些先前未知化合物的结构均通过其光谱研究和元素分析得到证实。筛选这些化合物的抗微生物和抗氧化活性。

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