Synthesis, characterization and biological activity studies of certain 1-((benzo[d]thiazol-2-yl) methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine and 2-((5-aryl-1H-1,2,4-triazol-3-yl) methyl)benzo[d]thiazoles

P. Uma, K. Rajanna, Firasath Unnisa, P. Saiprakash
{"title":"Synthesis, characterization and biological activity studies of certain 1-((benzo[d]thiazol-2-yl) methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine and 2-((5-aryl-1H-1,2,4-triazol-3-yl) methyl)benzo[d]thiazoles","authors":"P. Uma, K. Rajanna, Firasath Unnisa, P. Saiprakash","doi":"10.1080/23312009.2017.1312673","DOIUrl":null,"url":null,"abstract":"Abstract In this work, 1-((benzo[d]thiazol-2-yl)methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine (3a-h) have been successfully synthesized from the condensation of 2-((Benzo[d]thiazol-2-1-((benzo[d]thiazol-2-yl)methyl)-3-methyl-1H-pyrazol-5(4H)-one (2) with different aromatic amines. On the other hand, in another protocol, cyclization of 2-(benzo[d]thiazol-2-yl) acetohydrazide (4) with different aromatic aldehydes afforded 2-((5-aryl-1H-1,2,4-triazol-3-yl)methyl)benzo[d]thiazoles (5a-h). A perusal of the biological activity studies revealed that the derivatives having chlorine as substituent are more toxic to all six bacteria. Among the chloro group compounds, the compound which has methoxy group is more toxic.","PeriodicalId":10640,"journal":{"name":"Cogent Chemistry","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23312009.2017.1312673","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cogent Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23312009.2017.1312673","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Abstract In this work, 1-((benzo[d]thiazol-2-yl)methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine (3a-h) have been successfully synthesized from the condensation of 2-((Benzo[d]thiazol-2-1-((benzo[d]thiazol-2-yl)methyl)-3-methyl-1H-pyrazol-5(4H)-one (2) with different aromatic amines. On the other hand, in another protocol, cyclization of 2-(benzo[d]thiazol-2-yl) acetohydrazide (4) with different aromatic aldehydes afforded 2-((5-aryl-1H-1,2,4-triazol-3-yl)methyl)benzo[d]thiazoles (5a-h). A perusal of the biological activity studies revealed that the derivatives having chlorine as substituent are more toxic to all six bacteria. Among the chloro group compounds, the compound which has methoxy group is more toxic.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
某些1-((苯并[d]噻唑-2-基)甲基)-4,5-二氢-3-甲基- n -苯基- 1h -吡唑-5-亚胺和2-((5-芳基- 1h -1,2,4-三唑-3-基)甲基)苯并[d]噻唑的合成、表征和生物活性研究
摘要本文以2-((苯并[d]噻唑-2-1-(苯并[d]噻唑-2-基)甲基)-3-甲基-1H-吡唑-5(4H)-酮(2)与不同芳香胺的缩合反应为原料,成功合成了1-(苯并[d]噻唑2-基)甲基-4,5-二氢-3-甲基-N-苯基-1H-吡嗪-5-亚胺(3a-h)。另一方面,在另一方案中,2-(苯并[d]噻唑-2-基)乙酰酰肼(4)与不同的芳族醛的环化得到2-((5-芳基-1H-1,2,4-三唑-3-基)甲基)苯并[d]噻唑(5a-h)。仔细阅读生物活性研究表明,以氯为取代基的衍生物对所有六种细菌的毒性都更大。在氯代化合物中,含甲氧基的化合物毒性较大。
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 去求助
来源期刊
Cogent Chemistry
Cogent Chemistry CHEMISTRY, MULTIDISCIPLINARY-
自引率
0.00%
发文量
0
期刊最新文献
Phytochemical screening, antibacterial and antioxidant activity studies on the crude root extract of Clematis hirsuta Synthesis of a new ionic liquid for efficient liquid/liquid extraction of lead ions from neutral aqueous environment without the use of extractants Quality and carotenoid compositions of extrudates produced from composite biofortified maize (Zea mays L.) and soybean (Glycine max (L.) Merr.) flours Human contact with phthalates during early life stages leads to weight gain and obesity Determination of antioxidant and antibacterial activities of leaf extracts of Plumbago zeylanica (Amira)
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1