One-pot multi-component synthesis of 2-amino-3-cyano-4,6-disubstituted pyridines using Fe3O4/HAP nanoacatalyst: a sustainable and greener approach

IF 3.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Shraddha V. Jadhav, Datta M. Gumatkar, Navnath T. Hatvate, Yatin U. Gadkari
{"title":"One-pot multi-component synthesis of 2-amino-3-cyano-4,6-disubstituted pyridines using Fe3O4/HAP nanoacatalyst: a sustainable and greener approach","authors":"Shraddha V. Jadhav,&nbsp;Datta M. Gumatkar,&nbsp;Navnath T. Hatvate,&nbsp;Yatin U. Gadkari","doi":"10.1007/s11164-026-06040-w","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, we report an innovative approach for the one-pot, multi-component synthesis of 2-amino-4,6-disubstituted-3-cyanopyridine derivatives via the cyclocondensation of aryl ketones, ammonium acetate, substituted aromatic aldehydes, and malononitrile in a neat environment using a prepared Fe<sub>3</sub>O<sub>4</sub>/HAP nanocatalyst. The prepared nanocatalyst was characterized using FTIR, XRD, TGA, and FE-SEM. The novelty of the current work is the preparation of magnetically recoverable Fe<sub>3</sub>O<sub>4</sub>/HAP nanocatalyst that selectively facilitates the multi-component synthesis of 3-cyanopyridine derivatives in neat conditions as a healthier and more sustainable alternative to the traditional catalytic systems. The newly developed protocol offers several significant benefits, including a shorter reaction time, very good yield of the desired product, lower temperatures, a wide range of substrates, and an easy separation process. Additionally, the catalyst was recovered and recycled for five cycles, resulting in a loss of catalytic activity.</p><h3>Graphical abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":753,"journal":{"name":"Research on Chemical Intermediates","volume":"52 8","pages":"5475 - 5493"},"PeriodicalIF":3.3000,"publicationDate":"2026-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research on Chemical Intermediates","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11164-026-06040-w","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Herein, we report an innovative approach for the one-pot, multi-component synthesis of 2-amino-4,6-disubstituted-3-cyanopyridine derivatives via the cyclocondensation of aryl ketones, ammonium acetate, substituted aromatic aldehydes, and malononitrile in a neat environment using a prepared Fe3O4/HAP nanocatalyst. The prepared nanocatalyst was characterized using FTIR, XRD, TGA, and FE-SEM. The novelty of the current work is the preparation of magnetically recoverable Fe3O4/HAP nanocatalyst that selectively facilitates the multi-component synthesis of 3-cyanopyridine derivatives in neat conditions as a healthier and more sustainable alternative to the traditional catalytic systems. The newly developed protocol offers several significant benefits, including a shorter reaction time, very good yield of the desired product, lower temperatures, a wide range of substrates, and an easy separation process. Additionally, the catalyst was recovered and recycled for five cycles, resulting in a loss of catalytic activity.

Graphical abstract

Abstract Image

Fe3O4/HAP纳米催化剂一锅多组分合成2-氨基-3-氰基-4,6-二取代吡啶:一种可持续和更环保的方法
在此,我们报告了一种创新的方法,通过芳基酮、乙酸铵、取代芳醛和丙二腈在整洁的环境中进行环缩合,在一锅中合成了多组分的2-氨基-4,6-二取代-3-氰吡啶衍生物。采用FTIR、XRD、TGA和FE-SEM对所制备的纳米催化剂进行了表征。本研究的新颖之处在于制备了磁性可回收的Fe3O4/HAP纳米催化剂,该催化剂选择性地促进了3-氰吡啶衍生物在整齐条件下的多组分合成,是传统催化体系更健康、更可持续的替代品。新开发的方案具有几个显着的优点,包括较短的反应时间,所需产品的收率非常高,温度较低,底物范围广,分离过程简单。此外,催化剂被回收并循环使用了5个循环,导致催化活性的损失。图形抽象
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
CiteScore
5.70
自引率
18.20%
发文量
229
审稿时长
2.6 months
期刊介绍: Research on Chemical Intermediates publishes current research articles and concise dynamic reviews on the properties, structures and reactivities of intermediate species in all the various domains of chemistry. The journal also contains articles in related disciplines such as spectroscopy, molecular biology and biochemistry, atmospheric and environmental sciences, catalysis, photochemistry and photophysics. In addition, special issues dedicated to specific topics in the field are regularly published.
×
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:604180095
Book学术官方微信
小红书