Synthesis and Structure of New Compounds NSAIDs-Like Using a Heterogeneous Recyclable Catalyst

A. Alkayal, Mohammad Keshe, R. Madwar, D. Sarko, Ayman Karam
{"title":"Synthesis and Structure of New Compounds NSAIDs-Like Using a Heterogeneous Recyclable Catalyst","authors":"A. Alkayal, Mohammad Keshe, R. Madwar, D. Sarko, Ayman Karam","doi":"10.18052/WWW.SCIPRESS.COM/ILCPA.68.82","DOIUrl":null,"url":null,"abstract":"In this research, Phenol derivatives have been reacted with aryl halides using 5 mol% Cu(I) Complex [CuClPPh3]4 as catalyst supported on Amberlyst A21. The typical reaction has been performed between p-cresol and bromobenzene. This reaction is achieved in o-xylene as solvent. However, the catalyst complex does not dissolve in o-xylene rather it acts as heterogeneous catalyst. Therefore, it is filtrated at the end of the reaction and reused several times. Accordingly, new compounds were prepared by reacting some of bromoaryl derivatives with some Phenol derivatives. It is anticipated that the synthesized compounds have a structure NSAIDs-likes that may find their applications in the pharmaceutical industries.","PeriodicalId":14453,"journal":{"name":"International Letters of Chemistry, Physics and Astronomy","volume":" 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Letters of Chemistry, Physics and Astronomy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18052/WWW.SCIPRESS.COM/ILCPA.68.82","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

In this research, Phenol derivatives have been reacted with aryl halides using 5 mol% Cu(I) Complex [CuClPPh3]4 as catalyst supported on Amberlyst A21. The typical reaction has been performed between p-cresol and bromobenzene. This reaction is achieved in o-xylene as solvent. However, the catalyst complex does not dissolve in o-xylene rather it acts as heterogeneous catalyst. Therefore, it is filtrated at the end of the reaction and reused several times. Accordingly, new compounds were prepared by reacting some of bromoaryl derivatives with some Phenol derivatives. It is anticipated that the synthesized compounds have a structure NSAIDs-likes that may find their applications in the pharmaceutical industries.
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
利用多相可回收催化剂合成非甾体抗炎药类新化合物及其结构
本研究以Amberlyst A21为载体,以5mol % Cu(I)络合物[CuClPPh3]4为催化剂,对苯酚衍生物与芳基卤化物进行了反应。对甲酚与溴苯之间进行了典型反应。该反应以邻二甲苯为溶剂进行。然而,催化剂配合物不溶于邻二甲苯,而是作为异相催化剂。因此,在反应结束时对其进行过滤,并多次重复使用。因此,一些溴芳基衍生物与一些酚衍生物反应制备了新的化合物。预计合成的化合物具有类似非甾体抗炎药的结构,在制药工业中有应用前景。
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
自引率
0.00%
发文量
0
期刊最新文献
Perturbation due to a Circumbinary Disc around L4,5 in the Photogravitational Elliptic Restricted Three-Body Problem The Planetary Vaporization Event Hypothesis: Supercharging Earth’s Geothermal Core, Identifying Side Effects Blast Patterns, and Inferring how to Find Earth-Like Planets or Identifying Super Charged Geothermal Cores and their Byproduct Blast Patterns Utilization of Agro-Waste in the Elimination of Dyes from Aqueous Solution: Equilibrium, Kinetic and Thermodynamic Studies Motion in the Restricted Three-Body Problem at the Nanoscale Synthesis and Evaluation of Thermodynamic Solubility of Triazolo Quinolone Class Derivatives in Various Solvents at 298.15-328.15 K
×
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:604180095
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