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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:微波辐射在多组分反应及其抗肿瘤和抗微生物活性下合成吡唑[3,4-B]吡啶。

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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 ?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:一个有效的单罐合成在多组分体系(MRCS)为吡唑并制备[3,4-B],从5-氨基-1-苯基-3-(吡啶-3-基)的反应吡啶衍生物 - 1H-吡唑用4-甲醛醛和P取代的酮酮或用丙酮酸和乙酸培养基中的一些芳香族醛。反应由两种不同的技术,常规加热和微波辐射进行。这些化合物筛选它们对革兰氏阳性菌的抗菌活性(芽孢杆菌属),革兰氏阴性细菌(大肠杆菌,阴沟泄殖腔和沙雷)和对枯萎病菌和扩展青霉抗真菌活性。此外,在对肝细胞系进行抗肿瘤活性测试的合成化合物4A-F中。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[3,4-B]吡啶-5-碳腈(4e)和4-(4-甲氧基苯基)-1-苯基-3,6-二(吡啶-3-基)-1H-吡唑[3,4-B]吡啶-5-腈(4A)显示出最高的活性。

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