Nano-Fe3O4@ZrO2-SO3H as highly efficient recyclable catalyst for the green synthesis of fluoroquinolones in ordinary or magnetized water
محورهای موضوعی : Iranian Journal of Catalysis
Ahmad Nakhaei
1
(
Young Researchers and Elite Club, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
)
Abolghasem Davoodnia
2
(
Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
)
Sepideh Yadegarian
3
(
Young Researchers and Elite Club, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
)
کلید واژه: Fluoroquinolones, Magnetized water, Fast and green synthesis, Fe3O4@ZrO2-SO3H, Ordinary water,
چکیده مقاله :
Core–shell zirconia-coated magnetite nanoparticle bearing sulfonic acid groups (nano-Fe3O4@ZrO2-H3PO4) have been prepared and used as an efficient acid catalyst in the synthesis of fluoroquinolons by the direct amination of 7-halo-6- fluoroquinolone-3-carboxylic acids with variety of piperazine derivatives and (4aR,7aR)-octahydro-1H-pyrrolo[3,4-b] pyridine. The reaction was carried out in the ordinary or magnetized water as a solvent. In the final outcomes, the nano-Fe3O4@ZrO2-SO3H showed good catalytic performance in the both forms of water. However, the magnetized water showed better results. Therefore, this new procedure provides prompt achievement to the appropriate products with acceptable yields in water as a green solvent at reflux situations with an easy work‐up process. Furthermore, the catalyst was recyclable and could be reused at least three times without any discernible loss in its catalytic activity.
[1] R. Breslow, Acc. Chem. Res. 24 (1991) 159-164.
[2] P.B. Fernandes, N. Shipkowitz, R.R. Bower, K.P. Jarvis, J. Weisz, D.T. Chu, J. Antimicrob. Chemother. 18 (1986) 693-701.
[3] K. Fujimaki, T. Noumi, I. Saikawa, M. Inoue, S. Mitsuhashi, Antimicrob. Agents Chemother. 32 (1988) 827-833.
[4] B. Llorente, F. Leclerc, R. Cedergren, Bioorg. Med. Chem. 4 (1996) 61-71.
[5] Y.-S. Oh, C.-W. Lee, Y.-H. Chung, S.-J. Yoon, S.-H. Cho, J. Heterocycl. Chem. 35 (1998) 541-550.
[6] R. Stahlmann, H. Lode, Drugs 58 (1999) 37-42.
[7] B.A. Lipsky, C.A. Baker, Clin. Infect. Dis. 28 (1999) 352-361.
[8] D.C. Hooper, J.S. Wolfson, N. Engl. J. Med. 324 (1991) 384-394.
[9] J.S. Wolfson, D.C. Hooper, Clin. Microbiol. Rev. 2 (1989) 378-424.
[10] A. Aubry, X.-S. Pan, L.M. Fisher, V. Jarlier, E. Cambau, Antimicrob. Agents Chemother. 48 (2004) 1281-1288.
[11] T.D. Gootz, R. Zaniewski, S. Haskell, B. Schmieder, J. Tankovic, D. Girard, P. Courvalin, R.J. Polzer, Antimicrob. Agents Chemother. 40 (1996) 2691-2697.
[12] L.A. Mitscher, Chem. Rev. 105 (2005) 559-592.
[13] F. Dubar, G. Anquetin, B. Pradines, D. Dive, J. Khalife, C. Biot, J. Med. Chem. 52 (2009) 7954-7957.
[14] A.V. Shindikar, C.L. Viswanathan, Bioorg. Med. Chem. Lett. 15 (2005) 1803-1806.
[15] D. Sriram, A. Aubry, P. Yogeeswari, L.M. Fisher, Bioorg. Med. Chem. Lett. 16 (2006) 2982-2985.
[16] I.W. Davies, L. Matty, D.L. Hughes, P.J. Reider, J. Am. Chem. Soc. 123 (2001) 10139-10140.
[17] M. Ledoux, C. Pham-Huu, Catal. Today 15 (1992) 263-284.
[18] C.S. Gill, B.A. Price, C.W. Jones, J. Catal. 251 (2007) 145-152.
[19] A. Nakhaei, A. Davoodnia, S. Yadegarian, Heterocycl. Lett. 7 (2017) 35-44.
[20] A. Nakhaei, A. Davoodnia, S. Yadegarian, Russ. J. Gen. Chem. 86 (2016) 2870-2876.
[21] A. Nakhaei, A. Davoodnia, A. Morsali, Res. Chem. Intermed. 41 (2015) 7815-7826.
[22] A. Nakhaei, A. Davoodnia, Chin. J. Catal. 35 (2014) 1761-1767.
[23] A. Nakhaei, Russ. J. Gen. Chem. 87 (2017) 1850-1856.
[24] M. Bakherad, A. Keivanloo, M. Gholizadeh, R. Doosti, M. Javanmardi, Res. Chem. Intermed. 43 (2017) 1013-1029.
[25] M.M. Hosseini, E. Kolvari, Chem. Lett. 46 (2017) 53-55.
[26] E.E. Platero, M.P. Mentruit, Catal. Lett. 30 (1994) 31-39.
[27] C. Garkoti, J. Shabir, S. Mozumdar, New J. Chem. 41 (2017) 9291-9298.
[28] P.L. Patnam, M. Bhatt, R. Singh, S. Saran, S.L. Jain, RSC Adv. 6 (2016) 60888-60895.
[29] A. Sarkar, S.K. Biswas, P. Pramanik, J. Mater. Chem. 20 (2010) 4417-4424.
[30] G.-Y. Li, Y.-R. Jiang, K.-L. Huang, P. Ding, L.-L. Yao, Colloid. Surf. A 320 (2008) 11-18.
[31] A.P. Kumar, J.H. Kim, T.D. Thanh, Y.-I. Lee, J. Mater. Chem. B 1 (2013) 4909-4915.
[32] M.A. Navarra, F. Croce, B. Scrosati, J. Mater. Chem. 17 (2007) 3210-3215.
[33] P.G. Reddy, S. Baskaran, Tetrahedron Lett. 42 (2001) 6775-6777.
[34] K. Kawakami, K. Namba, M. Tanaka, N. Matsuhashi, K. Sato, M. Takemura, Antimicrob. Agents Chemother. 44 (2000) 2126-2129.
[35] K. Grohe, H. Heitzer, Liebigs Ann. Chem. 1987 (1987) 29-37.
[36] I. Hayakawa, T. Hiramitsu, Y. Tanaka, Chem. Pharm. Bull. 32 (1984) 4907-4913.
[37] B. Guruswamy, R. Arul, Lett. Drug Des. Discov. 10 (2013) 86-93.
[38] Y.R. Kumar, V.V.N.K.V. Prasad Raju, R.R. Kumar, S. Eswaraiah, K. Mukkanti, M.V. Suryanarayana, M.S. Reddy, J. Pharm. Biomed. Anal. 34 (2004) 1125-1129.
