Preparation and Characterization of Co (II) Supported on Modified Magnetic Fe₃O₄ Nanoparticles and Its Application as Catalyst for the Synthesis of 2-Amino-3-Cyanopyridines

References

• N. Hussain-Khil, A. Ghorbani-Choghamarani, and M. Mohammadi, “A New Silver Coordination Polymer Based on 4,6-Diamino-2-Pyrimidinethiol: Synthesis, Characterization and Catalytic Application in Asymmetric Hantzsch Synthesis of Polyhydroquinolines,” Scientific Reports 11, no. 1 (2021): 15657.
   PubMed Web of Science ®Google Scholar
• M. Nikoorazm, M. Mohammadi, and M. Khanmoradi, “Zirconium@Guanine@MCM‐41 Nanoparticles: An Efficient Heterogeneous Mesoporous Nanocatalyst for One‐Pot, Multi‐Component Tandem Knoevenagel Condensation–Michael Addition–Cyclization Reactions,” Applied Organometallic Chemistry 34, (2020): e5704.
   Web of Science ®Google Scholar
• T. Tamoradi, M. Mohammadi, A. R. Kiasat, J. Davarpanah, and B. Karmakar, “A Competent, Atom-Efficient and Sustainable Synthesis of Bis-Coumarin Derivatives Catalyzed over Strontium-Doped Asparagine Modified Graphene Oxide Nanocomposite,” Polycyclic Aromatic Compounds (2021): 1–15.doi: 10.1080/10406638.2021.1998149
   Web of Science ®Google Scholar
• M. Mohammadi, M. Khodamorady, B. Tahmasbi, K. Bahrami, and A. Ghorbani-Choghamarani, “Boehmite Nanoparticles as Versatile Support for Organic–Inorganic Hybrid Materials: Synthesis, Functionalization, and Applications in Eco-Friendly Catalysis,” Journal of Industrial and Engineering Chemistry 97, (2021): 1–78.
   Web of Science ®Google Scholar
• S. Y. Mansour, G. H. Sayed, M. I. Marzouk, and S. S. Shaban, “Synthesis and Anticancer Assessment of Some New 2-Amino-3-Cyanopyridine Derivatives,” Synthetic Communications 51, (2021): 1–11.
   Web of Science ®Google Scholar
• N. Kumar, A. Chauhan, and S. Drabu, “Synthesis of Cyanopyridine and Pyrimidine Analogues as New anti-Inflammatory and Antimicrobial Agents,” Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie 65, no. 5 (2011): 375–80.
   PubMed Web of Science ®Google Scholar
• F. Zhang, Y. Zhao, L. Sun, L. Ding, Y. Gu, and P. Gong, “Synthesis and Anti-Tumor Activity of 2-Amino-3-Cyano-6-(1H-indol-3-yl)-4-Phenylpyridine Derivatives in Vitro,” European Journal of Medicinal Chemistry 46, no. 7 (2011): 3149–57.
   PubMed Web of Science ®Google Scholar
• A. A. Bekhit, and A. M. Baraka, “Novel Milrinone Analogs of Pyridine-3-Carbonitrile Derivatives as Promising Cardiotonic Agents,” European Journal of Medicinal Chemistry 40, no. 12 (2005): 1405–13.
   PubMed Web of Science ®Google Scholar
• T. Murata, M. Shimada, S. Sakakibara, T. Yoshino, H. Kadono, T. Masuda, M. Shimazaki, T. Shintani, K. Fuchikami, K. Sakai, et al. “Discovery of Novel and Selective IKK-β Serine-Threonine Protein Kinase Inhibitors. Part 1,” Bioorganic & Medicinal Chemistry Letters 13, no. 5 (2003): 913–8.
   PubMed Web of Science ®Google Scholar
• M. A. Gouda, M. A. Berghot, G. E. Abd El Ghani, and A. E.-G. M. Khalil, “Chemistry of 2-Amino-3-Cyanopyridines,” Synthetic Communications 44, no. 3 (2014): 297–330.
   Web of Science ®Google Scholar
• A. M. Shestopalov, and O. A. Naumov, “Synthesis of Substituted 2-Amino-3-Cyano-7, 9-diMethyl-4 H-Pyrano [2", 3": 4, 5] Thieno [2, 3-b] Pyridines,” Russian Chemical Bulletin 52, (2003): 1380–5.
   Web of Science ®Google Scholar
• A. N. Vasiliev, Y. S. Kayukov, O. E. Nasakin, A. N. Lyshchikov, V. N. Nesterov, O. V. Kayukova, and O. V. Poulkherovskaya, “Synthesis of Alkyl 5,6-Dialkyl-2-Amino-3-Cyanopyridine-4-Carboxylates,” Chemistry of Heterocyclic Compounds 37, no. 3 (2001): 309–14.
   Google Scholar
• M. M. Heravi, S. Yahya Shirazi Beheshtiha, M. Dehghani, and N. Hosseintash, “Using Magnetic Nanoparticles Fe3O4 as a Reusable Catalyst for the Synthesis of Pyran and Pyridine Derivatives via One-Pot Multicomponent Reaction,” Journal of the Iranian Chemical Society 12, no. 11 (2015): 2075–81.
   Web of Science ®Google Scholar
• S. S. Mansoor, K. Aswin, K. Logaiya, P. N. Sudhan, and S. Malik, “Aqueous Media Preparation of 2-Amino-4,6-Diphenylnicotinonitriles Using Cellulose Sulfuric Acid as an Efficient Catalyst,” Research on Chemical Intermediates 40, no. 2 (2014): 871–85.
   Web of Science ®Google Scholar
• A. A. Dissanayake, R. J. Staples, and A. L. Odom, “Titanium-Catalyzed, One-Pot Synthesis of 2-Amino-3-Cyano- Pyridines,” Advanced Synthesis & Catalysis 356, no. 8 (2014): 1811–22.
   Web of Science ®Google Scholar
• M. A. Zolfigol, M. Kiafar, M. Yarie, A. Taherpour, and M. Saeidi-Rad, “Experimental and Theoretical Studies of the Nanostructured {Fe3O4@SiO2@(CH2)3Im}C(CN)3 Catalyst for 2-Amino-3-Cyanopyridine Preparation: Via an Anomeric Based Oxidation,” RSC Advances 6, no. 55 (2016): 50100–11.
   Web of Science ®Google Scholar
• T. Akbarpoor, A. Khazaei, J. Y. Seyf, N. Sarmasti, and M. M. Gilan, “One-Pot Synthesis of 2-Amino-3-Cyanopyridines and Hexahydroquinolines Using Eggshell-Based Nano-Magnetic Solid Acid Catalyst via Anomeric-Based Oxidation,” Research on Chemical Intermediates 46, no. 2 (2020): 1539–54.
   Web of Science ®Google Scholar
• R. Khalifeh, and M. Ghamari, “A Multicomponent Synthesis of 2-Amino-3-Cyanopyridine Derivatives Catalyzed by Heterogeneous and Recyclable Copper Nanoparticles on Charcoal,” Journal of the Brazilian Chemical Society 27, (2016): 759–68.
   Web of Science ®Google Scholar
• D. Khalili, “Graphene Oxide: A Reusable and Metal-Free Carbocatalyst for the One-Pot Synthesis of 2-Amino-3-Cyanopyridines in Water,” Tetrahedron Letters 57, no. 15 (2016): 1721–3.
   Web of Science ®Google Scholar
• J. Tang, L. Wang, Y. Yao, L. Zhang, and W. Wang, “One-Pot Synthesis of 2-Amino-3-Cyanopyridine Derivatives Catalyzed by Ytterbium Perfluorooctanoate [Yb(PFO)3],” Tetrahedron Letters 52, no. 4 (2011): 509–11.
   Web of Science ®Google Scholar
• A. Ghorbani-Choghamarani, R. Sahraei, Z. Taherinia, and M. Mohammadi, “Cu(I)@Isatin-Glycine-Boehmite Nanoparticles: As Novel Heterogeneous Catalyst for the Synthesis and Selective Oxidation of Sulfides,” Journal of the Iranian Chemical Society 18, no. 4 (2020): 827–838.
   Web of Science ®Google Scholar
• S. Schauermann, N. Nilius, S. Shaikhutdinov, and H.-J. Freund, “Nanoparticles for Heterogeneous Catalysis: New Mechanistic Insights,” Accounts of Chemical Research 46, no. 8 (2013): 1673–81.
   PubMed Web of Science ®Google Scholar
• V. Polshettiwar, and R. S. Varma, “Green Chemistry by Nano-Catalysis,” Green Chemistry 12, no. 5 (2010): 743–54.
   Web of Science ®Google Scholar
• T. Tamoradi, S. Masoumeh Mousavi, and M. Mohammadi, “C − C and C − S Coupling Catalyzed by Supported Cu(II) on Nano CoFe 2 O 4,” ChemistrySelect 5, no. 17 (2020): 5077–81.
   Web of Science ®Google Scholar
• A. Ghorbani-Choghamarani, M. Mohammadi, and Z. Taherinia, “(ZrO)2Fe2O5 as an Efficient and Recoverable Nanocatalyst in C–C Bond Formation,” Journal of the Iranian Chemical Society 16, no. 2 (2019): 411–21.
   Web of Science ®Google Scholar
• H. Filian, A. Kohzadian, M. Mohammadi, A. Ghorbani‐Choghamarani, and A. Karami, “Pd(0)‐Guanidine@MCM‐41: A Very Effective Catalyst for Rapid Production of Bis (Pyrazolyl)Methanes,” Applied Organometallic Chemistry 34, (2020): e5579.
   Web of Science ®Google Scholar
• M. Mohammadi, and A. Ghorbani-Choghamarani, “L-Methionine–Pd Complex Supported on Hercynite as a Highly Efficient and Reusable Nanocatalyst for C–C Cross-Coupling Reactions,” New Journal of Chemistry 44, no. 7 (2020): 2919–29.
   Web of Science ®Google Scholar
• A. Ghorbani-Choghamarani, H. Aghavandi, and M. Mohammadi, “Mesoporous SBA-15@n-Pr-THAM-ZrO Organic–Inorganic Hybrid: As a Highly Efficient Reusable Nanocatalyst for the Synthesis of Polyhydroquinolines and 2,3-Dihydroquinazolin-4 (1h)-Ones,” Journal of Porous Materials 28 (2021): 1167-1186.
   Web of Science ®Google Scholar
• A. Ghorbani-Choghamarani, Z. Taherinia, and M. Mohammadi, “Facile Synthesis of Fe3O4@GlcA@Ni-MOF Composites as Environmentally Green Catalyst in Organic Reactions,” Environmental Technology & Innovation 24, (2021): 102050.
   Web of Science ®Google Scholar
• X. Duan, J. Liu, J. Hao, L. Wu, B. He, Y. Qiu, J. Zhang, Z. He, J. Xi, and S. Wang, “Magnetically Recyclable Nanocatalyst with Synergetic Catalytic Effect and Its Application for 4-Nitrophenol Reduction and Suzuki Coupling Reactions,” Carbon N Carbon 130, (2018): 806–13.
   Web of Science ®Google Scholar
• Z. Esam, M. Akhavan, A. Bekhradnia, M. Mohammadi, and S. Tourani, “A Novel Magnetic Immobilized Para-Aminobenzoic Acid-Cu(II) Complex: A Green, Efficient and Reusable Catalyst for Aldol Condensation Reactions in Green Media,” Catalysis Letters 150, no. 11 (2020): 3112–31.
   Web of Science ®Google Scholar
• A. Khazaei, N. Sarmasti, and J. Y. Seyf, “Waste to Wealth: Conversion of Nano-Magnetic Eggshell (Fe3O4@Eggshell) to Fe3O4@Ca(HSO4)2: Cheap, Green and Environment-Friendly Solid Acid Catalyst,” Applied Organometallic Chemistry 32, no. 4 (2018): e4308.
   Web of Science ®Google Scholar
• A. Khazaei, N. Sarmasti, and J. Yousefi Seyf, “Anchoring High Density Sulfonic Acid Based Ionic Liquid on the Magnetic Nano-Magnetite (Fe3O4), Application to the Synthesis of Hexahydroquinoline Derivatives,” Journal of Molecular Liquids 262, (2018): 484–94.
   Web of Science ®Google Scholar
• S. Andalibi Salem, A. Khazaei, J. Y. Seyf, N. Sarmasti, and M. Mahmoudiani Gilan, “Preparation of Magnetic Cu(II) Nano-Structure (Based on Nano-Fe3O4) and Application to the Synthesis of Hexahydroquinoline Derivatives,” Polycyclic Aromatic Compounds 41, no. 2 (2021): 319–32. doi: 10.1080/10406638.2021.1873152
   Web of Science ®Google Scholar
• T. Akbarpour, J. Yousefi Seyf, A. Khazaei, and N. Sarmasti, “Synthesis of Pyrano [2,3-c] Pyrazole Derivatives Using a Novel Ionic-Liquid Based Nano-Magnetic Catalyst (Fe3O4@SiO2@(CH2)3NH@CC@Imidazole@SO3H + Cl−),” Polycyclic Aromatic Compounds (2021): 1–21.
   Google Scholar
• M. Kazemi, and M. Mohammadi, “Magnetically Recoverable Catalysts: Catalysis in Synthesis of Polyhydroquinolines,” Applied Organometallic Chemistry 34, (2020): e5400.
   Web of Science ®Google Scholar
• A. Ghorbani-Choghamarani, M. Mohammadi, L. Shiri, and Z. Taherinia, “Synthesis and Characterization of Spinel FeAl2O4 (Hercynite) Magnetic Nanoparticles and Their Application in Multicomponent Reactions,” Research on Chemical Intermediates 45, no. 11 (2019): 5705–23.
   Web of Science ®Google Scholar