氟苯甲酸酰胺的合成及其抑菌活性

U. Issayeva, G. S. Akhmetova, K. Praliyev, U. Datkhayev, М.Т. Omyrzakov, R.B. Seidahmetova, D.A. Abdambayev, T. Seilkhanov
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摘要

有机氟化合物的化学,在一代人的眼皮下,已经从有机化学的一个小分支变成了一个具有极其重要的理论和实践意义的独立的大分支。许多研究证实,一些含氟有机化合物具有很高的生物活性,因此,诸如氟喹诺酮类抗生素、利培酮、氟非那嗪、氟哌啶醇等药物已被创造出来并成功使用。在酰胺类衍生物中,已发现具有抗菌、抗惊厥、镇痛和抗真菌特性的物质。本工作的目的是开发一些新的具有潜在生物活性的含氟酰胺的方法,并研究它们的生物活性。结果与讨论:在环胺-啉的基础上,与对、间、邻氟苯甲酰氯酰化,根据Schotten-Bauman反应,合成了相应的对、间、邻氟苯甲酸酰胺。反应在无水苯中进行,经冷却,胺与酰化剂的比例为2:1。得到了与b-环糊精包合的化合物。通过元素分析、红外光谱、核磁共振光谱和薄层色谱对合成化合物的组成和结构进行了确证。合成的化合物在代码ПМП-4 - ПМП-6下进行了体外抑菌活性研究。所有化合物对革兰氏阳性和革兰氏阴性菌株均表现出明显的抗菌活性,特别是对金黄色葡萄球菌ATCC 6538的革兰氏阳性菌株表现出中等活性。该化合物ПМП-6对革兰氏阳性菌枯草芽孢杆菌具有中等活性,对革兰氏阴性试验菌株大肠杆菌ATCC 25922具有中等抑菌作用。该化合物ПМП-6还具有抗酵母菌白色念珠菌ATCC 10231的抗真菌活性。
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Synthesis and antimicrobial activity of fluorobenzoic acid amides
The chemistry of organofluorine compounds, before the eyes of one generation, has turned from a small branch of organic chemistry into a large independent branch of exceptionally important theoretical and practical significance. Numerous studies have confirmed the high biological activity of a number of fluorine-containing organic compounds, as a result of which such drugs as fluoroquinolone antibiotics, risperidone, fluorophenazine, haloperidol, etc. have been created and are successfully used. Among amide derivatives, substances with antibacterial, anticonvulsant, analgesic and antifungal properties have been found. The purpose of this work is to develop ways to obtain a number of new potentially biologically active fluorine-containing amides based on morpholine, and to study their biological activity. Results and discussion: on the basis of cyclic amine - morpholine, by acylation with para-, meta-, ortho-fluorobenzoyl chlorides, reaction according to Schotten-Bauman, the corresponding amides of para-, meta-, ortho-fluorobenzoic acids were synthesized. The reaction was carried out in absolute benzene with cooling and the ratio of amine: acylating agent = 2:1. Inclusion complexes of compounds with b-cyclodextrin have been obtained. The composition and structure of the synthesized compounds were confirmed by data of elemental analysis and IR, NMR spectroscopy, individuality - by thin-layer chromatography. The synthesized compounds under the codes ПМП-4 - ПМП-6 were studied in an in vitro experiment for antimicrobial activity. All compounds exhibit pronounced antibacterial activity against the presented gram-positive and gram-negative test strains, in particular, they exhibit moderate activity against the gram-positive strain of Staphylococcus aureus ATCC 6538. The compound ПМП-6 exhibits moderate activity against gram-positive bacteria Bacillus subtilis and moderate antibacterial action against the gram-negative test strain Escherichia coli ATCC 25922. The compound ПМП-6 also has antifungal activity against the yeast fungus Candida albicans ATCC 10231.
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