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2-溴-5-氯噻吩的一锅法选择性芳基化;通过密度泛函理论(DFT)、X射线分析对分子结构的研究及其生物活性

One Pot Selective Arylation of 2-Bromo-5-Chloro Thiophene; Molecular Structure Investigation via Density Functional Theory (DFT), X-ray Analysis, and Their Biological Activities.

作者信息

Rasool Nasir, Kanwal Aqsa, Rasheed Tehmina, Ain Quratulain, Mahmood Tariq, Ayub Khurshid, Zubair Muhammad, Khan Khalid Mohammed, Arshad Muhammad Nadeem, M Asiri Abdullah, Zia-Ul-Haq Muhammad, Jaafar Hawa Z E

机构信息

Department of Chemistry, Government College University Faisalabad, Faisalabad 38000, Pakistan.

Department of Chemistry, COMSATS Institute of Information Technology, University Road, Tobe Camp, Abbottabad 22060, Pakistan.

出版信息

Int J Mol Sci. 2016 Jun 28;17(7):912. doi: 10.3390/ijms17070912.

Abstract

Synthesis of 2,5-bisarylthiophenes was accomplished by sequential Suzuki cross coupling reaction of 2-bromo-5-chloro thiophenes. Density functional theory (DFT) studies were carried out at the B3LYP/6-31G(d, p) level of theory to compare the geometric parameters of 2,5-bisarylthiophenes with those from X-ray diffraction results. The synthesized compounds are screened for in vitro bacteria scavenging abilities. At the concentration of 50 and 100 μg/mL, compounds 2b, 2c, 2d, 3c, and 3f with IC50-values of 51.4, 52.10, 58.0, 56.2, and 56.5 μg/mL respectively, were found most potent against E. coli. Among all the synthesized compounds 2a, 2d, 3c, and 3e with the least values of IC50 77, 76.26, 79.13 μg/mL respectively showed significant antioxidant activities. Almost all of the compounds showed good antibacterial activity against Escherichia coli, whereas 2-chloro-5-(4-methoxyphenyl) thiophene (2b) was found most active among all synthesized compound with an IC50 value of 51.4 μg/mL. All of the synthesized compounds were screened for nitric oxide scavenging activity as well. Frontier molecular orbitals (FMOs) and molecular electrostatic potentials of the target compounds were also studied theoretically to account for their relative reactivity.

摘要

通过2-溴-5-氯噻吩的连续铃木交叉偶联反应完成了2,5-二芳基噻吩的合成。在B3LYP/6-31G(d, p)理论水平上进行了密度泛函理论(DFT)研究,以比较2,5-二芳基噻吩的几何参数与X射线衍射结果的几何参数。对合成的化合物进行体外细菌清除能力筛选。在50和100μg/mL的浓度下,发现化合物2b、2c、2d、3c和3f对大肠杆菌最有效,其IC50值分别为51.4、52.10、58.0、56.2和56.5μg/mL。在所有合成化合物中,IC50值最低的2a、2d、3c和3e分别为77、76.26、79.13μg/mL,显示出显著的抗氧化活性。几乎所有化合物对大肠杆菌都表现出良好的抗菌活性,而2-氯-5-(4-甲氧基苯基)噻吩(2b)在所有合成化合物中活性最高,IC50值为51.4μg/mL。还对所有合成化合物进行了一氧化氮清除活性筛选。还从理论上研究了目标化合物的前沿分子轨道(FMOs)和分子静电势,以解释它们的相对反应活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/b9f2a228b631/ijms-17-00912-sch001.jpg

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