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首页> 外文期刊>Quimica nova >SYNTHESIS OF 2-(2-PYRIDYL)QUINOLINES PROMOTED BY MICROWAVES AND THEIR ANTIFUNGAL ACTIVITIES
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SYNTHESIS OF 2-(2-PYRIDYL)QUINOLINES PROMOTED BY MICROWAVES AND THEIR ANTIFUNGAL ACTIVITIES

机译:微波促进的2-(2-吡啶基)喹啉的合成及其抗真菌活性

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In this work a series of 2-(2- pyridyl)quinolines were prepared via a Povarov reaction between anilines, 2-pyridinocarbadehyde and ethyl vinyl ether under microwaves heating conditions. The optimized conditions herein reported allowed the preparation of several pyridylquinolines in yields in the range of 30-83%, some of them not previously accessible by this multicomponent process. The reported methodology has advantage over previous report due to its larger scope and short reaction time (2 hours). All quinolines obtained were assayed against five species of clinically important yeasts Candida sp and against Cryptococcus neoformans. Some of them possessed a broad spectrum of action including 2-(2-pyridyl)quinoline (20) and 6,8-dimethoxy-2-(pyridin-2-yl)quinolone (22) that were highly effective in inhibiting Candida species (IC50 1.95 μg/mL against C. tropicalis and C. krusei). Some compounds were more potent than commercial drugs Nistatin and Miconazole.
机译:在这项工作中,在微波加热条件下,通过苯胺,2-吡啶基氨基甲酸酯和乙基乙烯基醚之间的Povarov反应制备了一系列2-(2-吡啶基)喹啉。本文报道的优化条件允许制备几种吡啶基喹啉,产率为30-83%,其中一些以前是该多组分方法无法获得的。所报告的方法由于具有更大的范围和较短的反应时间(2小时)而具有优于先前报告的优势。针对五种临床上重要的酵母念珠菌和新隐球菌对所有获得的喹啉进行了测定。其中一些具有广泛的作用范围,包括2-(2-吡啶基)喹啉(20)和6,8-二甲氧基-2-(吡啶-2-基)喹诺酮(22),它们在抑制念珠菌物种方面非常有效(针对热带念珠菌和克鲁斯梭菌的IC50 <1.95μg/ mL)。一些化合物比商业药物尼他汀和咪康唑更有效。

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