吡啶羧酸、吖啶和吡唑酮杂环衍生物的合成新方法

D. V. Kazak, E. Dikusar, S. Stepin
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引用次数: 0

摘要

现代药物化学的紧迫任务是发展新的合成方法,研究化学性质,以及在烟酸和异烟酸的衍生物中寻找生物活性化合物。本报告审查了生产羧酸酯的合成方法,包括烟酸和异烟酸,并举例说明烟酸和异烟酸及其衍生物的生物活性。讨论了偶氮亚胺、取代吖啶和吡唑啉酮的合成方法,并举例说明了它们的生物活性。提出了以烟酸和异烟酸的杂环衍生物为基础合成有潜力的新药物的前景。本文综述了烟酸和异烟酸杂环衍生物的有机化合物功能化方法,为获得具有抗菌、抗病毒、杀真菌和抗肿瘤活性的新化合物提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NEW APPROACHES TO SYNTHESIS OF HETEROCYCLIC DERIVATIVES OF PYRIDINE CARBOXYLIC ACIDS, ACRIDINE AND PYRAZOLONE
The urgent task of modern pharmaceutical chemistry is the development of new methods of synthesis, the study of chemical properties, as well as the search for biologically active compounds among derivatives of nicotinic and isonicotinic acids. The review examines synthetic approaches to the production of carboxylic acid esters including nicotinic and isonicotinic acids, gives examples of the biological activity of nicotinic and isonicotinic acids and their derivatives. The methods for the synthesis of azomethines, substituted acridines and pyrazolones are discussed, examples of their biological activity are given. A promising concept for the synthesis of new potential drugs based on heterocyclic derivatives of nicotinic and isonicotinic acids is presented. The methods of functionalization of organic compounds considered in this review with regard to the synthesis of heterocyclic derivatives of nicotinic and isonicotinic acids make it possible to obtain new promising compounds potentially having antibacterial, antiviral, fungicidal and antitumor activity.
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