Catalytic Synthesis of 3-Methyl-1-phenyl-1H-benzo[g]pyrazolo[3,4-b]quinoline-5,10-dione Derivatives Using Cerium Oxide Nanoparticles as Heterogeneous Catalyst in Green Conditions
We have developed a new methodology for the synthesis of 3-methyl-1-phenyl-1H-benzo[g]pyrazolo[3,4-b]quinoline-5,10-dione derivatives in excellent yields. A new green chemistry protocol with the reusability of the nanoparticle as catalyst has been developed for the synthesis of 3-methyl-1-phenyl-1H-benzo[g]pyrazolo[3,4-b]quinoline-5,10-dione derivatives via one-pot reaction of 3-methyl-1-phenyl-1H-pyrazol-5-amine, arylaldehydes, and 2-hydroxynaphthalene-1,4-dione in water as green solvent and using cerium oxide nanoparticles (CONPs) as heterogeneous catalyst. The present methodology affords several advantages such as simple procedure, excellent yields, and short reaction time. The catalyst is inexpensive, stable, easily recycled, and reused for several cycles with consistent activity. 1. Introduction Pyrazolo[3,4-b]quinoline derivatives are used as pharmaceutical agents [1], as inhibitors of oncogenic Ras [2], and as a dopant in the multiplayer OLED fabrication [3]. In the past several decades, three general strategies for the synthesis of pyrazolo[3,4-b]quinolines have been developed: (1) by the Friedlander condensation reaction of 2-aminobenzophenones and pyrazolin-5-ones [4]. Availability of 2-aminobenzophenones limits the range of applicability of this reaction; (2) by cyclization of 4-arylidenepyrazolin-5-ones with anilines [5] or 5-N-arylpyrazoles with aromatic aldehydes [6]. The method is complicated and has a lower yield; (3) by a three-component one-pot reaction of aromatic aldehydes, 5-amino-3-methyl-1-phenylpyrazole, and dimedone under thermal [7] or microwave condition [8]. Nanoparticles have emerged as sustainable alternatives to conventional materials and as robust, high-surface-area heterogeneous catalyst supports. The presence of a catalyst is mainly required by both modern organic syntheses and in fine chemical industries. Thus, the chemical nature and the existing form of the catalyst are of vital importance for the reaction. Recently, a great deal of attention has been focused on satisfying the requirements of environmentally benign and sustainable developments [8]. Consequently, there is a great demand for the discovery and development of novel catalysts with higher catalytic activities, lower prices, good recyclability, and less pollution to the environment in their catalytic systems. Cerium oxide has been extensively used in catalytic converters for automobile exhaust systems as an ultraviolet absorber and as an electrolyte for fuel cells [9–12]. Cerium-oxide based materials are famous for their redox properties, because of
References
[1]
O. A. El-Sayed and H. Y. Aboul-Enein, “Synthesis and antimicrobial activity of novel pyrazolo[3, 4-b]quinoline derivatives,” Archiv der Pharmazie, vol. 334, pp. 117–120, 2001.
[2]
R. Wolin, D. Wang, J. Kelly et al., “Synthesis and evaluation of pyrazolo[3,4-b]quinoline ribofuranosides and their derivatives as inhibitors of oncogenic Ras,” Bioorganic and Medicinal Chemistry Letters, vol. 6, no. 2, pp. 195–200, 1996.
[3]
Z. He, G. H. W. Milburn, K. J. Baldwin, D. A. Smith, A. Danel, and P. Tomasik, “The efficient blue photoluminescence of pyrazolo-[3,4-b]-quinoline derivatives and the energy transfer in polymer matrices,” Journal of Luminescence, vol. 86, no. 1, pp. 1–14, 2000.
[4]
K. Chaczatrian, G. Chaczatrian, A. Danel, and P. Tomasik, “The synthesis of 4-aryl-1H-pyrazolo[3,4-b]quinolines by cyclization of 4-arylidenepyrazolin-5-ones with anilines,” Arkivoc, vol. 2001, no. 6, pp. 63–69, 2001.
[5]
A. Danel, K. Chaczatrian, and P. Tomasik, “Microwave-assisted, facile route to 1H-pyrazolo[3,4-b]quinolines,” Arkivoc, vol. 2000, no. 1, pp. 51–57, 2000.
[6]
J. Quiroga, B. Insuasty, A. Hormaza, C. Saitz, and C. Jullian, “Synthesis of 4-Aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-ones,” Journal of Heterocyclic Chemistry, vol. 35, no. 3, pp. 575–578, 1998.
[7]
G.-P. Hua, J.-N. Xu, S.-J. Tu et al., “Facile three component one-pot synthesis of 5-aryl-1,5,6,7,8,9-hexahydro- 2H-pyrazolo[5,4-b]quinolin-6-one derivatives under microwave irradiation,” Chinese Journal of Organic Chemistry, vol. 25, no. 12, pp. 1610–1614, 2005.
[8]
C. K. Z. Andrade and L. M. Alves, “Environmentally benign solvents in organic synthesis: current topics,” Current Organic Chemistry, vol. 9, no. 2, pp. 195–218, 2005.
[9]
Z. Liu, R. Zhou, and X. Zheng, “Comparative study of different methods of preparing CuO-CeO2 catalysts for preferential oxidation of CO in excess hydrogen,” Journal of Molecular Catalysis A, vol. 267, no. 1-2, pp. 137–142, 2007.
[10]
S. Hilaire, X. Wang, T. Luo, R. J. Gorte, and J. Wagner, “A comparative study of water-gas-shift reaction over ceria-supported metallic catalysts,” Applied Catalysis A, vol. 258, no. 2, pp. 271–276, 2004.
[11]
M. Chen, P. Z. Zhang, and X. M. Zheng, “A new preparation method for nano-sized Ce-Zr-Ba mixed oxide with high surface area,” Catalysis Today, vol. 93-95, pp. 671–974, 2004.
[12]
T. Masui, M. Yamamoto, T. Sakata, H. Mori, and G.-Y. Adachi, “Synthesis of BN-coated CeO2 fine powder as a new UV blocking material,” Journal of Materials Chemistry, vol. 10, no. 2, pp. 353–357, 2000.
[13]
A. Tschope, W. Liu, M. Flytzanistephanopoulos, and J. Y. Ying, “Redox activity of nonstoichometric cerium oxide based nanocrystalline catalysts,” Journal of Catalysis, vol. 157, no. 1, pp. 42–50, 1995.
[14]
I. Celardo, E. Traversa, and L. Ghibelli, “Cerium oxide nanoparticles: a promise for applications in therapy,” Journal of Experimental Therapeutics and Oncology, vol. 9, no. 1, pp. 47–51, 2011.
[15]
K. Sambasivudu, Y. B. Reddy, J. S. Yadav, G. Sabitha, and D. Shailaja, “Ceria-supported vinylpyridine polymers: synthesis, characterization and application in catalysis,” International Journal of Polymeric Materials, vol. 57, no. 9, pp. 891–903, 2008.
[16]
A. Trovarelli, Catalysis by Ceria and Related Materials, Imperial College Press, London, UK, 2002.
[17]
J. A. Wang, J. M. Dominguez, A. Montoya et al., “New insights into the defective structure and catalytic activity of Pd/ceria,” Chemistry of Materials, vol. 14, no. 11, pp. 4676–4683, 2002.
[18]
A. Corma, P. Atienzar, H. García, and J.-Y. Chane-Ching, “Hierarchically mesostructured doped CeO2 with potential for solar-cell use,” Nature Materials, vol. 3, no. 6, pp. 394–397, 2004.
[19]
B. Akhlaghinia, H. Ebrahimabadi, E. K. Goharshadi, S. Samiee, and S. Rezazadeh, “Ceria nanoparticles as an efficient catalyst for oxidation of benzylic CH bonds,” Journal of Molecular Catalysis A, vol. 357, pp. 67–72, 2012.