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Microwave-assisted preparation andantimicrobial activity of O-alkylaminobenzofurancarboxylates

机译:微波辅助制备和O-烷基氨基的抗菌活性苯并呋喃羧酸盐

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摘要

AbstractA series of derivatives of 2 and 3-benzofurancarboxylates were synthesized under microwave-assisted conditions. Their in-vitro antimicrobial properties were assessed. Inhibition by the compounds of the growth of antibiotic-susceptible standards and clinically isolated strains of Gram-positive and Gram-negative bacteria, yeasts, and a human fungal pathogen was moderate to significant. Methyl 5-bromo-7-[2-(N,N-diethylamino)ethoxy]-6-methoxy-2-benzofurancarboxylate hydrochloride was identified as the most active compound (MIC 3–12 × 10−3 μmol/cm3 against Gram-positive bacteria; MIC 9.4 × 10−2 μmol/cm3 against Candida and Aspergillus brasiliensis). The molecular and crystal structures of 2-(N,N-diethylamino)ethyl 6-acetyl-5-hydroxy-2-methyl-3-benzofurancarboxylate were established by single-crystal X-ray diffraction.
机译:摘要在微波辅助条件下合成了2和3-苯并呋喃羧酸酯的一系列衍生物。他们的体外抗菌性能进行了评估。化合物对抗生素敏感标准的生长以及临床分离的革兰氏阳性和革兰氏阴性细菌,酵母菌和人类真菌病原体的抑制作用为中度至显着。 5-溴-7- [2-(N,N-二乙基氨基)乙氧基] -6-甲氧基-2-苯并呋喃甲酸甲酯盐酸盐被鉴定为活性最高的化合物(MIC 3-12×10 -3 革兰氏阳性菌>μmol/ cm 3 ;念珠菌和巴西曲霉的MIC 9.4×10 −2 μmol/ cm 3 。通过单晶X射线衍射建立了2-(N,N-二乙氨基)乙基6-乙酰基-5-羟基-2-甲基-3-苯并呋喃羧酸酯的分子和晶体结构。

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