...
首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >DABCOmediated one pot synthesis of 2-(3-benzyl-2, 6-dioxo-3, 6-dihydropyrimidin-1[2H]-yl)-N-(4-(1,3-dioxo-1H-benzo [de]isoquinolin-2[3H]-yl) aryl) acetamides as antimicrobial agents
【24h】

DABCOmediated one pot synthesis of 2-(3-benzyl-2, 6-dioxo-3, 6-dihydropyrimidin-1[2H]-yl)-N-(4-(1,3-dioxo-1H-benzo [de]isoquinolin-2[3H]-yl) aryl) acetamides as antimicrobial agents

机译:DABCOMEDIE化的一个罐合成2-(3-苄基-2,6-二氧基-3,6-二氢嘧啶-1 [2H] - ell)-N-(4-(1,3-二氧基-1H-苯并[de] 异喹啉-2 [3H] - yl)芳基)乙酰胺作为抗微生物剂

获取原文
获取原文并翻译 | 示例
           

摘要

We report herein DABCO mediated one pot synthesis of2-(3-benzyl-2,6-dioxo-3,6-dihydropyrimidin-1[2H]-yl)-N-(4-(1,3-dioxo-1H-benzo[de]isoquinolin-2[3H]-yl) aryl) acetamides (4a-j). The silent features of this new one pot synthesis include the shorter reaction time, high yields, simple workup, and simultaneous formation ofN-Amide andN-benzyl bonds in the one pot. The newly synthesized compounds (4a-j) were characterized by different spectral techniques such as IR,H-1-NMR,C-13-NMR, HRMS. All the synthesized compounds were evaluated for their anti-bacterial and anti-fungal activities. The anti-bacterial activities results reveal that the compounds4a,4g,4i, and4jare most active againstS. aureus. In the case ofB. subtilisthe compounds4a,4i, and4jare found to be most active. The compounds4c,4e,4i, and4jare most active againstE. coli. In the case ofP. aeruginosa4a,4i & 4jare found to be more active. On the other hand, the anti-fungal activity result shows that the compounds4d,4f,4i, and4jare more active againstA. niger. The compounds4a,4d,4i, and4jare found to be more active againstC. albicans.
机译:我们在此报告DABCO介导的一个罐合成2-(3-苄基-2,6-二氧基-3,6-二氢嘧啶-1 [2H] - ell)-N-(4-(1,3-二氧氧-1H-苯并[de]异喹啉-2 [3H] - 乙基)芳基)乙酰胺(4a-j)。这种新的一个罐合成的沉默特征包括较短的反应时间,高产率,单纯的余量和一个罐中的酰胺And苄基键的同时形成。新合成的化合物(4A-J)的特征在于IR,H-1-NMR,C-13-NMR,HRMS等不同的光谱技术。评估所有合成的化合物,用于其抗细菌和抗真菌活性。抗细菌活性结果表明,化合物4a,4g,4i,和4jare最活跃的反对。金黄色葡萄球菌。在ofb的情况下。发现枯草芽孢杆菌化合物4a,4i,和4jare发现最活跃。化合物4c,4e,4i,和4jare最活跃的反对。大肠杆菌。在OFP的情况下。铜绿假单胞菌4a,4i&4jare发现更活跃。另一方面,抗真菌活性结果表明,化合物4d,4f,4i,和4jare更活跃。尼日尔。发现化合物4a,4d,4i,和4jare发现更加活跃。老年人。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号