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This study successfully demonstrates the application of GO/IL/Zn Cl as a novel and environmentally friendly catalyst for the synthesis of 2-amino-3-cyanopyridine derivatives. Using husk as a precursor, a hybrid catalyst combining graphene oxide (GO), ionic liquid (IL), and zinc chloride-based species (Zn Cl ) was produced, exhibiting higher catalytic activity, better selectivity, and outstanding recyclability. The structural and morphological features of GO/IL/Zn Cl were investigated using FT-IR spectroscopy, Raman spectroscopy, XRD analysis, ICP-MS analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and thermogravimetric analysis (TGA) to elucidate their properties and establish the catalyst's efficiency and stability in organic synthesis. Under solvent-free conditions, we investigated the adaptability of the catalyst by effectively synthesizing of 2-amino-3-cyanopyridine derivatives with moderate to high yields (up to 57%), at 110 °C for 40 min. Analysis of the electronic and steric effects of different substituents revealed that electron-donating groups improve yield while electron-withdrawing groups reduce it, thereby offering insightful information for further catalyst modifications. The sustainability of the approach was determined by applying green chemistry criteria. The key indicators highlighting notable waste reduction and effective resource use were an E-factor of 1.40, an atom economy of 73.44%, and a process mass intensity (PMI) of 2.40. GO/IL/Zn Cl provides a possible substitute for sustainable organic synthesis owing to its excellent catalytic efficiency, selectivity, recyclability, and eco-friendly nature.
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http://dx.doi.org/10.1039/d5ra04734j | DOI Listing |
RSC Adv
August 2025
Department of Organic Chemistry, Faculty of Chemistry, University of Science Ho Chi Minh City 700000 Vietnam +84-908-108-824.
This study successfully demonstrates the application of GO/IL/Zn Cl as a novel and environmentally friendly catalyst for the synthesis of 2-amino-3-cyanopyridine derivatives. Using husk as a precursor, a hybrid catalyst combining graphene oxide (GO), ionic liquid (IL), and zinc chloride-based species (Zn Cl ) was produced, exhibiting higher catalytic activity, better selectivity, and outstanding recyclability. The structural and morphological features of GO/IL/Zn Cl were investigated using FT-IR spectroscopy, Raman spectroscopy, XRD analysis, ICP-MS analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and thermogravimetric analysis (TGA) to elucidate their properties and establish the catalyst's efficiency and stability in organic synthesis.
View Article and Find Full Text PDFRSC Adv
July 2025
Department of Chemistry, Basic of Sciences Faculty, Ilam University 69315-516 Ilam Iran
In this study, we successfully utilized natural asphalt as a natural carbon substrate for the synthesis of a novel heterogeneous Brønsted acid nanocatalyst, Re-NA-CHCOH. The -COOH functional groups present on the surface of Reduced Natural Asphalt Oxide (Re-NA-oxide) serve as catalytic sites for Brønsted acid. This arrangement, in addition to increasing acidity, also expands the surface area accessible for catalytic activity, positioning Re-NA-oxide as a viable option for a range of acid-catalyzed reactions.
View Article and Find Full Text PDFSci Rep
January 2023
Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan, Iran.
A new heterogeneous nanocatalyst LDH@3-chloropyltrimethoxysilane@1,3-benzenedisulfonyl amine@Cu (LDH@TRMS@BDSA@Cu) was synthesized and confirmed by analyzes such as Fourier transform infrared spectroscopy, Field Emission Scanning Electron Microscopy, energy scattered X-ray spectroscopy (EDX), elemental mapping, X-ray diffraction analysis, heat gravity/heat derivatization (TGA) and differential scanning calorimetry. The newly synthesized nanocatalyst effectively catalyzed the reaction between different aryl aldehydes, malononitrile, different acetophenones and ammonium acetate in solvent-free conditions and they were converted into 2-amino-3-cyanopyridine derivatives with high efficiency. The reaction showed advantages such as simplicity, high stability, environmental friendliness, excellent efficiency and short time.
View Article and Find Full Text PDFMolecules
May 2022
Laboratoire de Catalyse et Synthèse en Chimie Organique, Faculté des Sciences, Université de Tlemcen, BP 119, Tlemcen 13000, Algeria.
Unlabelled: A new and suitable multicomponent one-pot reaction was developed for the synthesis of 2-amino-3-cyanopyridine derivatives.
Background: This synthesis was demonstrated by the efficient and easy access to a variety of substituted 2-aminopyridines using enaminones as key precursors under solvent-free conditions.
Methods: A range of spectroscopic techniques was used to determine and confirm the chemical structures (FTIR, H NMR, C NMR).
Future Med Chem
August 2020
Department of Oncology, Nanjing First Hospital Nanjing Medical University, Nanjing, 210042, China.
To clarify the molecular mechanism of novel 2-aminonicotinonitrile autophagy enhancers, two series of novel 2-aminonicotinonitrile derivatives are synthesized and their structure-activity relationship and biological activity were analyzed. Structure-activity relationship analysis revealed that substituents at C-4 and C-6 position of contribute to enhance their autophagy-inducing activity, while C-5 position substituents have the opposite effect. The most promising compound showed the strongest autophagy-inducing activity and better antiproliferative activity by inducing cell apoptosis and blocking cell cycle G1 arrest in SGC-7901 cells.
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