微波辐射在含4- 1噻唑烷嘧啶类似物合成中的意义:体外抗菌、抗结核和抗疟疾研究

IF 0.9 Q4 CHEMISTRY, MULTIDISCIPLINARY Current Microwave Chemistry Pub Date : 2020-08-31 DOI:10.2174/2213335607999200918155613
N. Patel, Hetal I. Soni, R. Parmar
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Present\nstudy aims to carry out a rapid synthesis of Thiazolidin-4-one derivative of pyrimidine by microwave-\nassisted heating.\n\n\n\n4-(4-substituted phenyl)-6-(substituted aryl) pyrimidin-2-amine was the key intermediate\nrequired for the synthesis of 3-(4-(Substituted phenyl)-6-(substituted aryl) pyrimidin-2-yl)-2-(4-hydroxy\nphenyl) thiozolidin-4-one (5A-J), which was prepared by using microwave irradiation. 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引用次数: 1

摘要

采用微波辐照法合成具有生物活性的噻唑烷-4- 1,并对不同种类的细菌、真菌和恶性疟原虫进行抑菌效果评价。微波辐照法适用于快速、可持续的合成。本研究采用微波辐照法合成了含4- 1噻唑烷嘧啶衍生物。噻唑烷-4- 1因其广谱生物学评价而成为一个有价值的基序。以抗菌、抗结核、抗惊厥、降压、降糖、抗疟疾等多种生物特性而闻名。这种生物学反应引起了我们对噻唑烷-4- 1骨架变化的关注,以增强潜力。研究了微波辅助加热快速合成噻唑烷-4- 1嘧啶衍生物的方法。4-(4-取代苯基)-6-(取代芳基)嘧啶-2-胺是微波辐射合成3-(4-(取代苯基)-6-(取代芳基)嘧啶-2-基)-2-(4-羟基苯基)噻唑烷-4-酮(5A-J)所需的关键中间体。对新合成的基序进行了结构表征(IR、1H NMR、13CNMR),并对大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和化脓性链球菌进行了抑菌活性筛选;对念珠菌、黑曲霉、克拉曲霉的抗真菌活性;对结核分枝杆菌ish37rv的抗结核活性和对恶性疟原虫的抗疟活性。收率高、耗时短是含噻唑烷酮嘧啶基序合成的主要优点。化合物5B、5C、5D、5G、5H、5I和5J具有良好的生物效应。与传统方法相比,利用微波辐照技术制备噻唑烷-4- 1类似物所需的时间更短。噻唑烷-4- 1衍生物具有较好的生物活性。
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Significance of Microwave Irradiation in Synthesis of Thiazolidin-4-one Bearing Pyrimidine Analogues: Their in vitro Antimicrobial, Antituberculosis and Antimalarial Studies
To synthesise biologically active thiazolidin-4-one by microwave irradiation method and evaluate against different species of bacteria, fungi and Plasmodium falciparum. Microwave irradiation method is serviceable for rapid and sustainable synthesis. In this present study, Thiazolidin-4-one bearing pyrimidine derivatives have been synthesized by microwave irradiation method. Thiazolidin-4-one is a valuable motif because of its broad-spectrum biological evaluation. It is famous for many types of biological profiles, mainly antimicrobial, anti-tuberculosis, anti- convulsant, antihypertensive, hypoglycemic agent and antimalarial. This biological response leads our attention towards the change of Thiazolidin-4-one skeleton to enhance potential. Present study aims to carry out a rapid synthesis of Thiazolidin-4-one derivative of pyrimidine by microwave- assisted heating. 4-(4-substituted phenyl)-6-(substituted aryl) pyrimidin-2-amine was the key intermediate required for the synthesis of 3-(4-(Substituted phenyl)-6-(substituted aryl) pyrimidin-2-yl)-2-(4-hydroxy phenyl) thiozolidin-4-one (5A-J), which was prepared by using microwave irradiation. The structures of all newly synthesized motifs were characterized by spectral analysis (IR, 1H NMR, 13C NMR spectroscopy) and screened for antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pyogenes; antifungal activity against Candida albicans, Aspergillus niger, Aspergillus Clavatus; anti-tuberculosis activity against M. tuberculosis H37RV and antimalarial activity against Plasmodium falciparum. Higher yield with less time-consuming method is the main advantage of Thiazolidin- 4-one bearing pyrimidine motifs synthesis. The excellent biological response of compounds 5B, 5C, 5D, 5G, 5H, 5I, and 5J was observed. As compared to conventional method, less time is required for the preparation of Thiazolidin- 4-one analogues by using advantageous microwave irradiation method. Thiazolidin-4-one derivatives showed improved biological activity.
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来源期刊
Current Microwave Chemistry
Current Microwave Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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