Microwave Assisted Groebke-Blackburn-Bienayme Multicomponent Reaction to Synthesis of Imidazo[1,2-a]pyridine-furan Hybrids as Possible Therapeutic Option for Leukemia, Colon Cancer and Prostate Cancer

Parth Manvar, Dharmesh Katariya, Amita Vyas, Pooja Bhanderi, R. Khunt
{"title":"Microwave Assisted Groebke-Blackburn-Bienayme Multicomponent Reaction to Synthesis of Imidazo[1,2-a]pyridine-furan Hybrids as Possible Therapeutic Option for Leukemia, Colon Cancer and Prostate Cancer","authors":"Parth Manvar, Dharmesh Katariya, Amita Vyas, Pooja Bhanderi, R. Khunt","doi":"10.2174/0122133356294226240228103251","DOIUrl":null,"url":null,"abstract":"\n\nMicrowave assisted ecofriendly catalytic protocol for the Groebke-Blackburn-Bienayme multicomponent reaction to synthesis imidazo[1,2-a]pyridine-furan hybrids as possible therapeutic option for leukemia, colon cancer and prostate cancer\n\n\n\nMicrowave synthesis has emerged as a potent tool for the more economical and environmentally friendly synthesis of organic compounds, such as derivatives of imidazo[1,2-a]pyridine. Compared to traditional synthesis, microwave radiation causes molecules to be excited and distributes thermal energy evenly in a shorter amount of time. Shorter response times and generally improved efficiency are the benefits of this.\n\n\n\nThe primary objective of the work presented in this article was to prepare imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated.\n\n\n\nIn a sealed microwave glass vial, 5-methylfuran-2-carbaldehyde 1, 2-aminoazines 2a-g, isocyanides 3a-c in presence of 20mol\n\n\n\nWe have successfully synthesised the imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. The structures of the compounds were confirmed through various spectroscopic techniques. Characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated.\n\n\n\nThe reported protocol is advantageous over conventional methods of imidazo[1,2-a]pyridine derivatives. The time required for the reaction is much less as compared to the usual requirements of reflux. Compound 4e, 4f, 4n and 4o shows the most increased activity against cell line RPMI-8226, HCT-116 and PC-3 of Leukemia, Colon cancer and Prostate cancer respectively. By using the potential of imidazo[1,2-a]pyridine-furan based compounds via sustainable green approach, more effective and accurate cancer treatments can be designed in future.\n\n\n\nNA\n","PeriodicalId":503957,"journal":{"name":"Current Microwave Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Microwave Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0122133356294226240228103251","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

Microwave assisted ecofriendly catalytic protocol for the Groebke-Blackburn-Bienayme multicomponent reaction to synthesis imidazo[1,2-a]pyridine-furan hybrids as possible therapeutic option for leukemia, colon cancer and prostate cancer Microwave synthesis has emerged as a potent tool for the more economical and environmentally friendly synthesis of organic compounds, such as derivatives of imidazo[1,2-a]pyridine. Compared to traditional synthesis, microwave radiation causes molecules to be excited and distributes thermal energy evenly in a shorter amount of time. Shorter response times and generally improved efficiency are the benefits of this. The primary objective of the work presented in this article was to prepare imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated. In a sealed microwave glass vial, 5-methylfuran-2-carbaldehyde 1, 2-aminoazines 2a-g, isocyanides 3a-c in presence of 20mol We have successfully synthesised the imidazo[1,2-a]pyridine-furan hybrids via Groebke-Blackburn-Bienayme multicomponent reaction using PEG 400 in microwave irradiation as green approach. The structures of the compounds were confirmed through various spectroscopic techniques. Characterized their anticancer activities against leukemia, colon cancer and prostate cancer are evaluated. The reported protocol is advantageous over conventional methods of imidazo[1,2-a]pyridine derivatives. The time required for the reaction is much less as compared to the usual requirements of reflux. Compound 4e, 4f, 4n and 4o shows the most increased activity against cell line RPMI-8226, HCT-116 and PC-3 of Leukemia, Colon cancer and Prostate cancer respectively. By using the potential of imidazo[1,2-a]pyridine-furan based compounds via sustainable green approach, more effective and accurate cancer treatments can be designed in future. NA
微波辅助格罗伯克-布莱克本-比奈梅多组分反应合成咪唑并[1,2-a]吡啶-呋喃杂化物,作为白血病、结肠癌和前列腺癌的可能治疗方案
微波辅助格罗伯克-布莱克本-比奈梅多组分反应的生态友好催化规程,用于合成咪唑并[1,2-a]吡啶-呋喃混合物,作为白血病、结肠癌和前列腺癌的可能治疗方案微波合成已成为一种更经济、更环保地合成有机化合物(如咪唑并[1,2-a]吡啶的衍生物)的有效工具。与传统合成法相比,微波辐射能在更短的时间内激发分子并均匀分配热能。本文研究的主要目的是通过格罗伯克-布莱克本-比奈梅多组分反应制备咪唑并[1,2-a]吡啶-呋喃混合物,采用 PEG 400 在微波辐照下作为绿色方法。在一个密封的微波玻璃瓶中,5-甲基呋喃-2-甲醛 1、2-氨基嗪 2a-g、异氰酸酯 3a-c 在 20 毫摩尔的存在下,我们利用 PEG 400 在微波辐照下进行多组分反应,成功合成了咪唑并[1,2-a]吡啶-呋喃杂化物。通过各种光谱技术确认了这些化合物的结构。与传统的咪唑并[1,2-a]吡啶衍生物制备方法相比,所报告的制备方法更具优势。与传统的回流法相比,所报告的方法更具优势。化合物 4e、4f、4n 和 4o 对白血病、结肠癌和前列腺癌细胞系 RPMI-8226、HCT-116 和 PC-3 的活性分别提高了很多。通过可持续绿色方法利用咪唑并[1,2-a]吡啶-呋喃类化合物的潜力,未来可以设计出更有效、更准确的癌症治疗方法。
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
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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