Construction of MWCNTs/MNPs-based copper nanocomposite as an efficient and reusable catalyst for four-component preparation of highly substituted pyridines

• High Yields and Broad Substrate Scope The method consistently delivers excellent yields (86–98%) across a wide variety of substrates. It tolerates a range of electron-donating and electron-withdrawing groups, making it highly versatile. • Efficient and Recyclable Catalyst The MWCNTs/MNPs-Tris(2-aminoethyl)amine-CuCl 2 nanocatalyst is heterogeneous, allowing for easy separation and potential reusability, thus reducing waste and cost. It exhibits excellent catalytic activity and stability throughout the process. • Operational Simplicity The method is one-pot and multicomponent, requiring no complex purification steps or elaborate setups. This increases feasibility for industrial scale-up and streamlines the synthesis process. A sustainable and highly efficient four-component protocol has been established for the synthesis of structurally diverse and highly substituted pyridine derivatives. The catalytic system, MWCNTs/MNPs–Tris(2-aminoethyl)amine–CuCl₂, effectively promotes the one-pot condensation of aromatic aldehydes, malononitrile, ethyl acetoacetate, and substituted anilines in aqueous medium under reflux conditions. This green catalytic method provides the desired pyridines in excellent yields (86–98%) within 1 hour, highlighting its remarkable activity and selectivity. The reaction system exhibits wide substrate compatibility, tolerating both electron-donating and electron-withdrawing substituents on the aromatic rings. Product identity and purity were confirmed by melting-point determination and observation of crystalline or oily characteristics. A comparative evaluation with existing protocols demonstrates significant advantages in yield, environmental compatibility, and operational simplicity. The use of water as an environmentally benign solvent, along with the recyclable magnetic nanocatalyst, underscores the method's sustainability and reusability. Overall, this approach provides a green, rapid, and practical route to valuable pyridine-based heterocycles with potential biological relevance.

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Publication Details

Journal
Journal of Organometallic Chemistry
Published
2026-01-03
DOI
https://doi.org/10.1016/j.jorganchem.2026.124011
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

Construction of MWCNTs/MNPs-based copper nanocomposite as an efficient and reusable catalyst for four-component preparation of highly substituted pyridines

Subhashree Ray, Rahul Kumar Sharma, Ahmed Kareem Obaid Aldulaimi, Mohamed Abu Shuheil et al.
Journal of Organometallic Chemistry
Multicomponent Synthesis of Heterocycles
article

Construction of MWCNTs/MNPs-based copper nanocomposite as an efficient and reusable catalyst for four-component preparation of highly substituted pyridines

Subhashree Ray, Rahul Kumar Sharma, Ahmed Kareem Obaid Aldulaimi, Mohamed Abu Shuheil, C.P. Surya, Vatsal Jain, Omayma Salim Waleed, Rekha MM
article en

Abstract

• High Yields and Broad Substrate Scope The method consistently delivers excellent yields (86–98%) across a wide variety of substrates. It tolerates a range of electron-donating and electron-withdrawing groups, making it highly versatile. • Efficient and Recyclable Catalyst The MWCNTs/MNPs-Tris(2-aminoethyl)amine-CuCl 2 nanocatalyst is heterogeneous, allowing for easy separation and potential reusability, thus reducing waste and cost. It exhibits excellent catalytic activity and stability throughout the process. • Operational Simplicity The method is one-pot and multicomponent, requiring no complex purification steps or elaborate setups. This increases feasibility for industrial scale-up and streamlines the synthesis process. A sustainable and highly efficient four-component protocol has been established for the synthesis of structurally diverse and highly substituted pyridine derivatives. The catalytic system, MWCNTs/MNPs–Tris(2-aminoethyl)amine–CuCl₂, effectively promotes the one-pot condensation of aromatic aldehydes, malononitrile, ethyl acetoacetate, and substituted anilines in aqueous medium under reflux conditions. This green catalytic method provides the desired pyridines in excellent yields (86–98%) within 1 hour, highlighting its remarkable activity and selectivity. The reaction system exhibits wide substrate compatibility, tolerating both electron-donating and electron-withdrawing substituents on the aromatic rings. Product identity and purity were confirmed by melting-point determination and observation of crystalline or oily characteristics. A comparative evaluation with existing protocols demonstrates significant advantages in yield, environmental compatibility, and operational simplicity. The use of water as an environmentally benign solvent, along with the recyclable magnetic nanocatalyst, underscores the method's sustainability and reusability. Overall, this approach provides a green, rapid, and practical route to valuable pyridine-based heterocycles with potential biological relevance.

Journal of Organometallic ChemistryVol. 1046
Chandigarh University (IN), Al-Ahliyya Amman University (JO), Jain University (IN), University of Mosul (IQ), Siksha O Anusandhan University (IN), Institute of Medical Sciences and Sum Hospital (IN), University of Kerbala (IQ), Sathyabama Institute of Science and Technology (IN), Chitkara University (IN)
Responsible consumption and production
Openalex Percentile: Top 98%
Multicomponent Synthesis of Heterocycles
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