Catalyst and Solvent Free Synthesis and Biological Activities of Imidazo[1,2-a]pyridine

G. B. Gundlewad, S. Wagh, B. R. Patil
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引用次数: 1

Abstract

A series of imidazo[1,2-a]pyridines were synthesized by the reaction of α-chloroacetophenone and 2- aminopyridine under catalyst and solvent free condition. The synthesized compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral data. These imidazo[1,2-a]pyridines were screened for antiinflammatory activity by carrageenan induced rat hind paw edema model. Good anti-inflammatory activity was shown by few compounds. The antibacterial activity was studied against two Grampositive bacteria S. aureus and B. subtilis, two Gram-negative bacteria E. coli and S. typhi and antifungal activity against P. chrysogenum, F. moneliforme, A. flavus and A. niger. All the synthesized compounds were desplayed good antimicrobial and antifungal activities. Some of the compounds were shown higher antibacterial activity than reference drug penicillin.
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咪唑[1,2-a]吡啶的无溶剂合成及生物活性研究
以α-氯苯乙酮和2-氨基吡啶为原料,在无催化剂和无溶剂条件下合成了一系列咪唑[1,2- A]吡啶。合成的化合物通过IR、1H NMR、13C NMR和质谱数据进行了表征。通过卡拉胶诱导大鼠后足水肿模型,筛选这些咪唑[1,2-a]吡啶类化合物的抗炎活性。少数化合物显示出良好的抗炎活性。研究了其对2种革兰氏阳性菌金黄色葡萄球菌和枯草芽孢杆菌、2种革兰氏阴性菌大肠杆菌和伤寒葡萄球菌的抑菌活性,以及对金黄色葡萄球菌、单念珠菌、黄芽孢杆菌和黑芽孢杆菌的抑菌活性。所有合成的化合物都显示出良好的抗菌和抗真菌活性。其中部分化合物的抑菌活性高于对照药青霉素。
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