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Microwave Assisted Heterocyclization: A Rapid and Efficient Synthesis and Antibacterial Activity of Novel Thiazolidinones

机译:微波辅助杂环:新型噻唑烷酮的快速有效的合成和抗菌活性

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摘要

As a target to synthesize various Thiazolidinone derivatives, 2-Amino-4-(coumarin-3-yl)-thiazole has been prepared by the reactions of 3-Bromo acetyl coumarin with thiourea. 3-Bromo acetyl coumarin was prepared from 3-Acetyl coumarin. The resulting compound 2-amino-4-(coumarin-3-yl)- thiazole was treated with different Aldehydes to give the intermediate Schiff base, which on further reaction with Thioglycolic acid and Thiolactic acid to give titled compound Thiazolidinone. The structures of the compounds have been confirmed by elemental analysis and spectral analysis. The antibacterial activity of the compounds has also been screened against Staphylococcus aureus and Escherichia coil.
机译:作为合成各种噻唑烷酮衍生物的靶标,通过3-溴乙酰氨基香豆素与硫脲的反应制备了2-氨基-4-(香豆素-3-基) - 噻唑。用3-乙酰基香豆素制备3-溴乙酰基香豆素。用不同的醛处理所得化合物2-氨基-4-(香豆素-3-基) - 噻唑,得到中间席夫碱,其在与巯基乙酸和硫酸甲酸的进一步反应中,得到标题的化合物噻唑烷酮。通过元素分析和光谱分析证实了化合物的结构。还针对金黄色葡萄球菌和大肠杆菌线圈筛分化合物的抗菌活性。

著录项

  • 作者

    B. D. Naik; K. R. Desai;

  • 作者单位
  • 年度 2004
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
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