Efficient one-pot synthesis of 6-amino-4-aryl-5-cyano-2-methyl-4H-pyran-3-carboxylates catalyzed by nano MgO in water

Publish Year: 1396
نوع سند: مقاله ژورنالی
زبان: English
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JR_ICC-6-2_003

تاریخ نمایه سازی: 2 مهر 1398

Abstract:

Water is a versatile solvent in many ways, and in this sense performing organic reactions in this medium is now of great interest. The one-pot reaction of ethyl acetoacetate or benzyl acetoacetate, with benzaldehydes and malononitrile to provide some novel 6-amino-4-aryl-5-cyano-2-methyl-4H-pyran-3-carboxylates has been performed over nano MgO with high performance in water as a green solvent at 80 °C. The nanocrystalline MgO catalyst was characterized via X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET analysis. This method offers considerable improvements for the synthesis of 6-amino-4-aryl-5-cyano-2-methyl-4H-pyran-3-carboxylates with concern to the yield of products, facility in operation, and green aspects without using of toxic catalysts and solvents.

Authors

Maryam Sojoudi

Department of Chemistry, Rasht Branch, Islamic Azad University, Rasht, Iran

Masoud Mokhtary

Islamic Azad University, Rasht branch, Iran

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  • P. Luches, S. Benedetti, M. Liberati, F. Boscherini, I.I. Pronin, ...
  • G. Bilalbegovic, Phys. Rev. B, 2004, 70, 45406-45407. ...
  • C.S. Goh, J. Wei, L.C. Lee, J. Compos. Mater., 2007, ...
  • G.A. Somorjai, J.Y. Park, Angew. Chem. Int. Ed., 2008, 47, ...
  • A. Martı´nez-Grau, J. Marco, Bioorg. Med. Chem. Lett., 1997, 7, ...
  • J.L. Wang, D. Liu, Z.J. Zhang, S. Shan, X. Han, ...
  • W. Kemnitzer, J. Drewe, S. Jiang, H. Zhang, C. Crogan-Grundy, ...
  • M. Kidwai, S. Saxena, M.K.R. Khan, S.S. Thukral, Bioorg. Med. ...
  • R.R. Kumar, S. Perumal, P. Senthilkumar, P. Yogeeswari, D. Sriram, ...
  • E.A. Hafez, M.H. Elnagdi, A.A. Elagamey, F.A. El-Taweel, Heterocycles, 1987, ...
  • D. Armesto, W.M. Horspool, N. Martin, A. Ramos, C. Seoane, ...
  • X.S. Wang, Z.S. Zeng, M.M. Zhang, Y.L. Li, D.Q. Shi, ...
  • Y. Peng, G. Song, F. Huang, Monatsh. Chem., 2005, 136, ...
  • M M. Heravi, Y.S. Beheshtiha, Z. Pirnia, S. Sadjadi, M. ...
  • N. Seshu Babu, N. Pasha, K.T. Venkateswara Rao, P.S. Sai ...
  • S. Banerjee, A. Horn, H. Khatri, G. Sereda, Tetrahedron Lett., ...
  • U.R. Pratap, D.V. Jawale, P.D. Netankar, R.A. Mane, Tetrahedron Lett., ...
  • G.P. Lu, C. Cai, J. Heterocycl. Chem., 2011, 48, 124-128. ...
  • C. Udhaya Kumar, A. Sethukumar, B. Arul Prakasam, J. Mol. ...
  • B. Maleki, S. Sheikh, Org. Prep. Proc. Int., 2015, 47, ...
  • A. Mossafaii Rad, M. Mokhtary, Int. Nano Lett., 2015, 5, ...
  • B. Karmakar, J. Banerji, Tetrahedron Lett., 2011, 52, 4957-4960. ...
  • J. Safari, Z. Zarnegar, M. Heydarian, J. Taibah. Unvi. Sci., ...
  • Z.X. Tang, X.J. Fang, Z.L. Zhang, T. Zhou, X.Y. Zhang, ...
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