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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of pyrazolo[3,4-b]pyridines under microwave irradiation in multi-component reactions and their antitumor and antimicrobial activities - Part 1.
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Synthesis of pyrazolo[3,4-b]pyridines under microwave irradiation in multi-component reactions and their antitumor and antimicrobial activities - Part 1.

机译:微波辐射下多组分反应中吡唑并[3,4-b]吡啶的合成及其抗肿瘤和抗菌活性-第1部分。

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摘要

An efficient one-pot synthesis in multi-component system (MRCs) for the preparation of pyrazolo[3,4-b]pyridine derivatives from the reaction of 5-amino-1-phenyl-3-(pyridin-3-yl)-1H-pyrazole with 4-anisaldehyde and p-substituted β-ketonitriles or with pyruvic acid and some aromatic aldehydes in acetic acid medium. The reactions were carried out by two different techniques, conventional heating and microwave irradiation. These compounds were screened for their antibacterial activity against Gram-positive bacteria (Bacillus), Gram-negative bacteria (Escherichia coli, Enterobacter cloaca and serratia) and antifungal activity against Fusarium Oxysporum and Penicillium expansum. Also, among the synthesized compounds 4a-f tested for antitumor activity against liver cell line. Compounds 6-(4-Fluorophenyl)-4-(4-methoxyphenyl)-1-phenyl-3-(pyridin-3-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile (4e) and 4-(4-Methoxyphenyl)-1-phenyl-3,6-di(pyridin-3-yl)-1H-pyrazolo[3,4-b] pyridine-5-carbonitrile (4a) showed the highest activity.
机译:一种有效的一锅多组分合成(MRC)方法,用于由5-氨基-1-苯基-3-(吡啶-3-基)-的反应制备吡唑并[3,4-b]吡啶衍生物1H-吡唑与4-茴香醛和对位取代的β-乙腈或在丙酮介质中与丙酮酸和一些芳族醛一起存在。反应通过两种不同的技术进行,常规加热和微波辐射。筛选了这些化合物对革兰氏阳性菌(芽孢杆菌),革兰氏阴性菌(大肠杆菌,泄殖腔肠杆菌和沙雷氏菌)的抗菌活性以及对镰孢镰刀菌和扩展青霉菌的抗真菌活性。另外,在合成的化合物4a-f中,测试了针对肝细胞系的抗肿瘤活性。化合物6-(4-氟苯基)-4-(4-甲氧基苯基)-1-苯基-3-(吡啶-3-基)-1H-吡唑并[3,4-b]吡啶-5-甲腈(4e)和4-(4-甲氧基苯基)-1-苯基-3,6-二(吡啶-3-基)-1H-吡唑并[3,4-b]吡啶-5-甲腈(4a)显示出最高的活性。

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