Synthesis and Characterization of New 1,2-Dihydropyridine-3-Carbonitrile Compounds with Study of Expected Biological Activity

H. Ibraheem, Y. Al-Majedy, A. Salim, R. Al-Bayati
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引用次数: 2

Abstract

New 1,2-dihydropyridine-3-carbonitrile derivative compounds (3,4) were synthesized by cyclization of ketones (compound (1) and compound (2)) with appropriate aldehydes (4-N, Ndimethylaminobenzaldehyde and 4-chloro-2-oxo-2H-chromene-3-carbaldehyde) in presence of ethyl cyano acetate and ammonium acetate. The new synthesized compounds have been characterized using Melting point, FT-IR spectroscopy and 1 H-NMR and 13 C-NMR spectrum. The evaluation of biological activity of some synthesized compounds (1-4) with different concentration 10 mg mL −1 , 1 mg mL −1 and 0.1 mg mL −1 , against two types of bacteria on gram positive bacterial Staphylococcus aureus, Streptococcus pyogenus and gram nagetive bacterial Escherichia coli, Klebsiella pneumniae. [DOI: 10.22401/JNUS.21.2.07]
1,2-二氢吡啶-3-碳腈新化合物的合成、表征及生物活性研究
在氰基乙酸乙酯和乙酸铵的存在下,将酮(化合物(1)和化合物(2)与适当的醛(4- n、二甲基氨基苯甲醛和4-氯-2-氧-2- h -铬-3-醛)环化,合成了新的1,2-二氢吡啶-3-碳腈衍生物(3,4)。用熔点、红外光谱、1h - nmr和13c - nmr对合成的化合物进行了表征。不同浓度(10 mg mL−1、1 mg mL−1和0.1 mg mL−1)合成的化合物(1-4)对革兰氏阳性细菌金黄色葡萄球菌、脓链球菌和革兰氏阴性细菌大肠杆菌、肺炎克雷伯菌的生物活性评价。(DOI: 10.22401 / JNUS.21.2.07)
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