Synthesis, characterization and antimicrobial activity of pyrimidine based derivatives

Yogesh Kumar Gupta , Vinita Gupta , Sanchita Singh
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引用次数: 24

Abstract

Aim

Pyrimidine and their derivatives play the vital role in the field of drugs and agricultural chemicals. In recent decades, a large no. of pharmacological studies has been done on Pyrimidine and their derivatives. But still more research is required in order to necessity of biological compounds. “The Chalcone is an aromatic compound that forms the central core for different necessity of biological compounds. The Chalcone is synthesized by an aldol, condensation of 4-methoxy acetophenone with m-phenoxy benzaldehydes in the presence of a catalyst that is treated with thiourea to provide Pyrimidine. The Pyrimidine treated with substituted N-1,3-benzothiazole-2-yl-2-chloro amide gives a compound”.

Methods

Elemental analysis, IR, H NMR, C NMR melting point, Thin layer chromatography (TLC) plates (silica gel G) is used to determine the purity of the compounds.

Result

Antimicrobial activity: All the synthesized compounds screened against four different strains, viz two Gram +ve bacteria (Staphylococcus aureus & Streptococcus pyogenes) and two Gram −ve bacteria (Escherichia coli & Pseudomonas aeruginosa), analyzed with standard drugs ampicillin, chloramphenicol, ciprofloxacin, & norfloxacin. Antifungal activities: All the synthesized compounds screened against Candida albicans, and Aspergillus niger organisms, analyzed with standard drugs nystatin and griseofulvin.

Conclusion

In this paper we focused on the reactions, synthesis, spectral analysis and Microbial activities of Pyrimidine based benzothiazole derivatives. The method gives excellent than previously reported literature. Some of the compounds were effective as antimicrobial and antifungal agents.

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嘧啶基衍生物的合成、表征及抗菌活性研究
aim嘧啶及其衍生物在药物和农用化学品领域发挥着重要作用。近几十年来,一个很大的数字是。对嘧啶及其衍生物进行了大量的药理研究。但为了证明生物化合物的必要性,还需要进行更多的研究。查尔酮是一种芳香化合物,它构成了不同生物化合物的核心。查尔酮是由4-甲氧基苯乙酮与间苯氧基苯甲醛在催化剂存在下缩合而成的,催化剂经硫脲处理得到嘧啶。用取代的n -1,3-苯并噻唑-2-基-2-氯酰胺处理的嘧啶得到化合物“。方法采用元素分析、IR、H - NMR、C - NMR熔点、薄层色谱(TLC)板(硅胶G)测定化合物纯度。结果:所有合成的化合物对4种不同的菌株,即2种革兰氏菌(金黄色葡萄球菌和葡萄球菌;化脓性链球菌)和两种革兰氏杆菌(大肠杆菌);铜绿假单胞菌),用标准药物氨苄西林、氯霉素、环丙沙星等进行分析;诺氟沙星。抗真菌活性:所有合成的化合物对白色念珠菌和黑曲霉生物进行了筛选,并与标准药物制霉菌素和灰黄霉素进行了分析。结论本文对嘧啶基苯并噻唑衍生物的反应、合成、光谱分析及微生物活性进行了综述。该方法比以往文献报道的结果更好。其中一些化合物是有效的抗菌和抗真菌剂。
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