Nickel ferrite as a recyclable nanocatalyst for synthesis of novel highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives

Publish Year: 1396
نوع سند: مقاله ژورنالی
زبان: English
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JR_ICC-6-1_011

تاریخ نمایه سازی: 2 مهر 1398

Abstract:

Highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives were synthesized by four-component reaction of aromatic aldehydes, malononitrile, ethyl acetoacetate and various phenylhydrazine, using nickel ferrite as a recyclable nanocatalyst by a grinding method under solvent-free and thermal conditions. The reaction has the advantages of good yields, less pollution, ease of separation of the desired products, and of being environment friendly. A possible mechanism for this reaction was proposed. Highly substituted 1,4-dihydropyrano[2,3-c]pyrazole derivatives were synthesized by four-component reaction of aromatic aldehydes, malononitrile, ethyl acetoacetate and various phenylhydrazine, using nickel ferrite as a recyclable nanocatalyst by a grinding method under solvent-free and thermal conditions. The reaction has the advantages of good yields, less pollution, ease of separation of the desired products, and of being environment friendly. A possible mechanism for this reaction was proposed.

Authors

Mohammad Reza Poor Heravi

Department of Chemistry, Payame Noor University, Abhar, Iran

Naheed Morsalie

aDepartment of Chemistry, Payame Noor University, PO Box ۱۹۳۹۵-۳۶۹۷, Tehran, IRAN

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  • C.N. Ocallaghan, T.B.H. Mcmurry, J. Chem. Res., 1999, (S) 8, ...
  • A.M. Shestopalov, N. Zukharal, D.H. Evans, M.E. Niyazgmbetov, Heterocycles, 1999, ...
  • D.  Armesto, A. Albert, F.H. Cano, N. Marrtin, A. Ramos, ...
  • J.L. Wang, D. Liu, Z.J. Zhang, S. Shan, X. Han, ...
  • L.N.  Martin, M. Quinterio, C. Seoane, J.L. Soto, Liebigs Annalen ...
  • S. Hatakeyama, N. Ochi, H. Numata, S. Takano, J. Chem. ...
  • M.R. Poor Heravi, ISRN Org. Chem, 2013, 52, 8329-8436. ...
  • X.S. Wang, D.Q. Shi, S.J. Tu, C.S. Yao, Y.C. Wang, ...
  • D. Shi, J. Mou, Q. Zhuang, L. Niu, N. Wu, ...
  • S. B. Guo, S.X. Wang, J.T. Li, Synth. Commun., 2007, ...
  • F. Tanaka, F. Toda, Chem. Rev., 2000, 100, 1025-1074.  ...
  • M.Z. Kassaee, F. Movahedi, H. Masouri, Synlett, 2009, 8, 1326-1330. ...
  • Z. Mirjafari, H. Saeidian, A. Sadeghi, F. Matloubo Moghaddam, Catal. ...
  • M. Stratakis, H. Garcia, Chem. Rev., 2012, 112 (8), 4460-4506. ...
  • K. Ablajan,Z.  Maimaiti, Synth. Commun., 2012, 42, 1959-1966. ...
  • H. Mecadon, M.R. Rohman, I. Kharbangar, B.M. Laloo, I. Kharkongor, ...
  • M. Babaie, H. Sheibani, Arab. J. Chem., 2011, 4, 159-162. ...
  • . Z. Karimi-Jaberi, M.M.  Reyazo Shams, B. Pooladian, Acta Chimica ...
  • H.R. Shaterian, M. Kangani, Res Chem. Intermed., 2014, 40, 1997-2005. ...
  • . M. Kangani, N. Hazeri, M.T. Maghsoodlou, S.M. Habibi-khorasani, S. ...
  • A.N. Siddekha, A.M. Pasha, Spectrochim. Acta. Chimica Slov, 2013, 60, ...
  • G. Kumar, R. Rani, S. Sharma, K.M. Batto, M. Singh, ...
  • P. Laokul, V. Amornkitbamrung, S. Seraphin, S. Maensiri, Curr. Appl. ...
  • J.M. Khurana, B. Nand, S. Kumar, Synth. Commun., 2011, 41, ...
  • R.S. Toreshettahally, S. Kothanahally, K. Sharath, P. Mariyappan, C. Somu, ...
  • V. Gnanasambandam, K. Kandhasamy, Tetrahedron Lett., 2008, 49, 5636-5638. ...
  • M. Abdollahi-Alibeik, A. Ali Moaddeli, K. Masoomi, RSC Advances, 2015, ...
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