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Synthesis, characterization and antimicrobial activity of novel xanthene sulfonamide and carboxamide derivatives

机译:新型x吨磺酰胺和羧酰胺衍生物的合成,表征和抗菌活性

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Abstract Xanthene intermediates 4a and 4b were obtained from the reduction of nitro xanthene derivatives 3a and 3b which were synthesized via condensation of dimedone with m-nitrobenzaldehyde and p-nitrobenzaldehyde, respectively. Then xanthene sulfonamide 6a–n , and xanthene carboxamide derivatives 8a–h were synthesized by reaction of amino xanthene 4a, 4b with sulfonyl chlorides 5a–g and acyl chlorides 7a–d . Structures of the novel amino xanthene compounds and xanthene sulfonamide/carboxamide derivatives were established by their spectral data and elemental analyses. Furthermore, all the synthesized compounds were tested in vitro for their antimicrobial activity. The results were compared with reference standard antibiotics, erythromycin and nystatin. 6c, 6f, 6m and 8b Compounds were found to display most effective antimicrobial activity against a series of bacteria and fungi.
机译:摘要分别通过二甲酮与间硝基苯甲醛和对硝基苯甲醛缩合反应合成的硝基x吨衍生物3a和3b还原得到obtained吨中间体4a和4b。然后通过氨基of吨4a,4b与磺酰氯5a-g和酰氯7a-d的反应合成x吨磺酰胺6a-n和x吨羧酰胺衍生物8a-h。通过光谱数据和元素分析,建立了新型氨基x吨化合物和x吨磺酰胺/羧酰胺衍生物的结构。此外,在体外测试了所有合成的化合物的抗菌活性。将结果与参考标准抗生素,红霉素和制霉菌素进行比较。发现6c,6f,6m和8b化合物对一系列细菌和真菌显示出最有效的抗菌活性。

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