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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Synthesis, characterization and antimicrobial studies of new 2-(2-chloroquinolin-3-yl)-3-(substituted phenyl/pyridinyl)quinazolin-4(3H)-one derivatives using l-proline as a catalyst
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Synthesis, characterization and antimicrobial studies of new 2-(2-chloroquinolin-3-yl)-3-(substituted phenyl/pyridinyl)quinazolin-4(3H)-one derivatives using l-proline as a catalyst

机译:以L-脯氨酸为催化剂的新型2-(2-氯喹啉-3-基)-3-(取代苯基/吡啶基)喹唑啉-4(3H)-一衍生物的合成,表征和抗菌研究

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摘要

2-(2-Chloroquinolin-3-yl)-3-(substituted phenyl/pyridinyl)quinazolin-4(3H)-one derivatives 5a-m were synthesized in good yield using conventional as well as microwave heating conditions in presence of l-proline as a catalyst. Synthetic conditions were optimized using an orthogonal array system of Taguchi's design. The structure of synthesized quinazolinone compounds 5a-m was established with the help of physico-chemical analysis and various spectroscopic techniques like FT-IR, mass, H-1-NMR and C-13-NMR. Further, all the synthesized compounds were screened for their antimicrobial (antibacterial, antifungal and antimalarial) activities. The results of antimicrobial screening showed that compounds 4g, 4j, 4m, 5e and 5g have good activity against bacterial species, whereas compounds 4d, 4g, 4m, 5b, 5d and 5g have good activity against malaria pathogen. In addition to this, compounds 4i, 4j and 4m exhibited good to moderate activity against fungal strains.
机译:在常规的和微波加热条件下,在l-存在下,以高收率合成了2-(2-氯喹啉-3-基)-3-(取代的苯基/吡啶基)喹唑啉-4(3H)-一衍生物5a-m。脯氨酸作为催化剂。使用田口设计的正交阵列系统优化了合成条件。借助物理化学分析和各种光谱技术(例如FT-IR,质谱,H-1-NMR和C-13-NMR)建立了合成的喹唑啉酮化合物5a-m的结构。此外,筛选所有合成的化合物的抗微生物(抗菌,抗真菌和抗疟疾)活性。抗菌筛选结果表明,化合物4g,4j,4m,5e和5g对细菌具有良好的活性,而化合物4d,4g,4m,5b,5d和5g对疟疾病原体具有良好的活性。除此之外,化合物4i,4j和4m对真菌菌株表现出良好至中等的活性。

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