Synthesis, characterization and biological activities of novel substituted formazans of 3,4-dimethyl-1H-pyrrole-2-carbohydrazide derivatives

Jitendra D. Bhosale , Amey R. Shirolkar , Umesh D. Pete , Chetan M. Zade , Dipesh P. Mahajan , Chakradhar D. Hadole , Sharad D. Pawar , Umesh D. Patil , Rajesh Dabur , R.S. Bendre
{"title":"Synthesis, characterization and biological activities of novel substituted formazans of 3,4-dimethyl-1H-pyrrole-2-carbohydrazide derivatives","authors":"Jitendra D. Bhosale ,&nbsp;Amey R. Shirolkar ,&nbsp;Umesh D. Pete ,&nbsp;Chetan M. Zade ,&nbsp;Dipesh P. Mahajan ,&nbsp;Chakradhar D. Hadole ,&nbsp;Sharad D. Pawar ,&nbsp;Umesh D. Patil ,&nbsp;Rajesh Dabur ,&nbsp;R.S. Bendre","doi":"10.1016/j.jopr.2013.07.022","DOIUrl":null,"url":null,"abstract":"<div><h3>Aim</h3><p>Synthesis of some novel formazan derivatives from condensation of aniline diazonium salt with a variety of Schiff bases of 3,4-dimethyl-1<em>H</em>-pyrrole-2-carbohydrazide moiety and evaluate their potential antimicrobial and antioxidant activities.</p></div><div><h3>Methods</h3><p>Novel substituted formazans <strong>(2a-j)</strong> were prepared from Schiff bases of 3,4-dimethyl-1<em>H</em>-pyrrole-2-carbohydrazide <strong>(1a-j)</strong> by condensation with aniline diazonium chloride in pyridine (<span>Scheme 1</span>). All the formazan derivatives were characterized by IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR and Mass spectroscopy.</p></div><div><h3>Results</h3><p>These molecules <strong>(2a-j)</strong> exhibits moderate to good antimicrobial and antioxidant activities some of which are comparable to standards used in this study.</p></div><div><h3>Conclusion</h3><p>The results of preliminary bioassays of derivatisation of Schiff bases to formazan indicate that a number of these molecules exhibits moderate to good antibacterial, antifungal and antioxidant activities some of which are comparable to standard used in this study. The outcome indicates that there is a good scope for evaluation of this class of compounds as potential leads towards antimicrobial and antioxidant agents.</p></div>","PeriodicalId":16787,"journal":{"name":"Journal of Pharmacy Research","volume":"7 7","pages":"Pages 582-587"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jopr.2013.07.022","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacy Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0974694313003046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16

Abstract

Aim

Synthesis of some novel formazan derivatives from condensation of aniline diazonium salt with a variety of Schiff bases of 3,4-dimethyl-1H-pyrrole-2-carbohydrazide moiety and evaluate their potential antimicrobial and antioxidant activities.

Methods

Novel substituted formazans (2a-j) were prepared from Schiff bases of 3,4-dimethyl-1H-pyrrole-2-carbohydrazide (1a-j) by condensation with aniline diazonium chloride in pyridine (Scheme 1). All the formazan derivatives were characterized by IR, 1H NMR, 13C NMR and Mass spectroscopy.

Results

These molecules (2a-j) exhibits moderate to good antimicrobial and antioxidant activities some of which are comparable to standards used in this study.

Conclusion

The results of preliminary bioassays of derivatisation of Schiff bases to formazan indicate that a number of these molecules exhibits moderate to good antibacterial, antifungal and antioxidant activities some of which are comparable to standard used in this study. The outcome indicates that there is a good scope for evaluation of this class of compounds as potential leads towards antimicrobial and antioxidant agents.

新型取代的3,4-二甲基- 1h -吡咯-2-碳酰肼衍生物的合成、表征及生物活性
目的由苯胺重氮盐与多种希夫碱3,4-二甲基- 1h -吡咯-2-碳酰肼段缩合合成新的甲氮酰胺衍生物,并评价其潜在的抗菌和抗氧化活性。方法以3,4-二甲基-1H-吡咯-2-碳肼(1a-j)的希夫碱为原料,与苯胺重氮氯化铵在吡啶(方案1)中缩合,制备新型取代甲醛衍生物(2a-j),并采用IR、1H NMR、13C NMR和质谱对其进行表征。结果这些分子(2a-j)具有中等至良好的抗菌和抗氧化活性,其中一些与本研究中使用的标准物相当。结论通过对希夫碱衍生成福马唑的初步生物测定表明,许多希夫碱衍生成的分子具有中等到良好的抗菌、抗真菌和抗氧化活性,其中一些分子具有与本研究中使用的标准分子相当的抗氧化活性。结果表明,这类化合物作为潜在的抗微生物剂和抗氧化剂有很好的评价范围。
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