Synthesis and Evaluation of 2-Chloro-3-[3-(6-Methyl-1H-Benzimidazol-2-Yl)-4, 5-Dihydro-1H-Pyrazol-5-Yl] Quinolines as Potent Antimicrobial Agents

B. Shivakumar, Indira. M. Madawali, S. Hugar, N. Kalyane
{"title":"Synthesis and Evaluation of 2-Chloro-3-[3-(6-Methyl-1H-Benzimidazol-2-Yl)-4, 5-Dihydro-1H-Pyrazol-5-Yl] Quinolines as Potent Antimicrobial Agents","authors":"B. Shivakumar, Indira. M. Madawali, S. Hugar, N. Kalyane","doi":"10.46624/ajphr.2018.v6.i12.004","DOIUrl":null,"url":null,"abstract":"A new series of 2-chloro-3-[3-(6-methyl-1H-benzimidazol-2-yl)-4,5-dihydro-1H-pyrazol-5yl]quinoline (Va-k) have been synthesized by the reaction of 3-(2-chloroquinolin-3-yl)-1-(6methyl-1H-benzimidazol-2-yl)prop-2-en-1-one (IVa-k) with hydrazine hydrate in ethanol and glacial acetic acid. The synthesized compounds were characterized by their IR, H NMR and Mass spectral studies. Further, compounds were screened for their antimicrobial activity by cup plate method, using Ciprofloxacin and Fluconazole as a standard drugs. Results of the activities reveal that, compounds exhibited moderate to good antibacterial and antifungal activities.","PeriodicalId":233230,"journal":{"name":"American Journal of Pharmacy And Health Research","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Pharmacy And Health Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46624/ajphr.2018.v6.i12.004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A new series of 2-chloro-3-[3-(6-methyl-1H-benzimidazol-2-yl)-4,5-dihydro-1H-pyrazol-5yl]quinoline (Va-k) have been synthesized by the reaction of 3-(2-chloroquinolin-3-yl)-1-(6methyl-1H-benzimidazol-2-yl)prop-2-en-1-one (IVa-k) with hydrazine hydrate in ethanol and glacial acetic acid. The synthesized compounds were characterized by their IR, H NMR and Mass spectral studies. Further, compounds were screened for their antimicrobial activity by cup plate method, using Ciprofloxacin and Fluconazole as a standard drugs. Results of the activities reveal that, compounds exhibited moderate to good antibacterial and antifungal activities.
2-氯-3-[3-(6-甲基- 1h -苯并咪唑-2-基)- 4,5 -二氢- 1h -吡唑-5-基]喹啉类强效抗菌药物的合成及评价
以3-(2-氯喹啉-3-基)-1-(6 -甲基- 1h -苯并咪唑-2-基)-4,5-二氢- 1h -吡唑-5基]喹啉(Va-k)为原料,在乙醇和冰醋酸中与水合肼反应合成了一系列新的2-氯-3-[3-(6-甲基- 1h -苯并咪唑-2-基)- 2-烯-1-酮(Va-k)。合成的化合物通过红外光谱、核磁共振光谱和质谱进行了表征。以环丙沙星和氟康唑为标准药物,采用杯盘法筛选化合物的抗菌活性。活性结果表明,化合物具有中等至良好的抗菌和抗真菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信