首页> 外文期刊>Pharmaceutical Chemistry Journal >Synthesis of N-Substituted (2,3-Dihydro-1,4-Benzodioxin-6-YL)Benzenesulfonamide Derivatives as Potent Antibacterial Agents and Moderate Enzyme Inhibitors
【24h】

Synthesis of N-Substituted (2,3-Dihydro-1,4-Benzodioxin-6-YL)Benzenesulfonamide Derivatives as Potent Antibacterial Agents and Moderate Enzyme Inhibitors

机译:合成N-取代的(2,3-二氢-1,4-苯并二辛-6-基)苯磺胺酰胺衍生物作为有效的抗菌剂和中度酶抑制剂

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The present research work involved the reaction of 2,3-dihydro-1,4-benzodioxin-6-amine (1) and benzenesulfonyl chloride (2) under dynamic pH control at 10 using aqueous Na2CO3. This reaction yielded 2,3-dihydro-1,4-benzodioxin-6-yl)benzenesulfonamide (3), which was further substituted at N-position with various alkyl/aryl halides (4a - 4m) in N,N-dimethylformamide and catalytic amount of lithium hydride to obtain N-substituted (2,3-dihydro-1,4-benzodioxin-6-yl)benzenesulfonamides (5a - 5m). The projected structures of the synthesized derivatives were confirmed using various spectral techniques (IR, 1H NMR and EIMS). The synthesized derivatives were screened for antibacterial potential and inhibitory activity against lipoxygenase enzyme.
机译:本研究工作涉及使用Na 2 CO 3水溶液在10的动态pH控制下反应2,3-二氢-1,4-苯并二辛-6-胺(1)和苯磺酰氯(2)。 该反应得到2,3-二氢-1,4-苯并二辛-6-基)苯磺酰胺(3),其在N-位置被在N,N-二甲基甲酰胺中的各种烷基/芳基卤化物(4A-4M)取代 催化量的氢化锂获得N-取代的(2,3-二氢-1,4-苯并二辛-6-基)苯磺胺酰胺(5a-5m)。 使用各种光谱技术(IR,1H NMR和EIM)确认合成衍生物的投影结构。 筛选合成的衍生物用于抗菌潜力和抑制脂氧酶酶的抑制活性。

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