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A Novel Method for Synthesis of 1,4-Dihydropyridines Using Robust Laterite Catalyst under Ultrasonic Irradiation
Corresponding Author(s) : C.S. Patil
Asian Journal of Chemistry,
Vol. 31 No. 1 (2019): Vol 31 Issue 1
Abstract
An efficient method for the synthesis of 1,4-dihydropyridine derivatives from various aryl or heteroaryl aldehydes, β-ketoester and ammonium acetate in presence of laterite catalyst in ethanol under ultrasonication is reported. Catalyst study done with wet chemical analysis, FT-IR, XRD, SEM and EDS techniques. The catalyst can be recovered and reused without noticeable loss of activity even after five cycles.
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References
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S. Das Sharma, P. Hazarika and D. Konwar, Catal. Commun., 9, 709 (2008); https://doi.org/10.1016/j.catcom.2007.08.008.
M. Litvic, I. Cepanec, M. Filipan, K. Kos, A. Bartolinèic, V. Druškovic, M. Majed Tibi and V. Vinkovic, Heterocycles, 65, 23 (2005); https://doi.org/10.3987/COM-04-10194.
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R.K. Singh, D.N. Prasad and T.R. Bhardwaj, Med. Chem. Res., 24, 1534 (2015); https://doi.org/10.1007/s00044-014-1236-1.
H.-A.S. Abbas, W.A. El-Sayed and N.M. Fathy, Eur. J. Med. Chem., 45, 973 (2010); https://doi.org/10.1016/j.ejmech.2009.11.039.
A. Hantzsch, J. Leibigs Ann. Chem., 215, 1 (1882); https://doi.org/10.1002/jlac.18822150102.
B. Loev and K.M. Snader, J. Org. Chem., 30, 1914 (1965); https://doi.org/10.1021/jo01017a048.
A. Dondoni, A. Massi, E. Minghini and V. Bertolasi, Tetrahedron, 60, 2311 (2004); https://doi.org/10.1016/j.tet.2004.01.011.
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A. Agarwal and P.M.S. Chauhan, Tetrahedron Lett., 46, 1345 (2005); https://doi.org/10.1016/j.tetlet.2004.12.109.
Mithlesh, P. Pareek, R. Kant, S.K. Shukla and K.G. Ojha, Cent. Eur. J. Chem., 8, 163 (2010); https://doi.org/10.2478/s11532-009-0114-z.
A.S. Paraskar and A. Sudalai, Indian J. Chem., 46B, 331 (2007).
C.A. Antonyraj and S. Kannan, Appl. Catal. A Gen., 338, 121 (2008); https://doi.org/10.1016/j.apcata.2007.12.028.
B. Datta and M.A. Pasha, Chin. J. Catal., 32, 1180 (2011); https://doi.org/10.1016/S1872-2067(10)60252-5.
D. Bandopadhyay, S. Maldonado and B.K. Banik, Molecules, 17, 2643 (2012); https://doi.org/10.3390/molecules17032643.
J. Ramchander, G. Raju, N. Rameshwar, T.S. Reddy and A.R. Reddy, Spectrochim. Acta A Mol. Biomol. Spectrosc., 85, 210 (2012); https://doi.org/10.1016/j.saa.2011.09.062.
L. Saikia, D. Dutta and D.K. Dutta, Catal. Commun., 19, 1 (2012); https://doi.org/10.1016/j.catcom.2011.12.013.
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C.L. Shi, H. Chen and D.Q. Shi, J. Heterocycl. Chem., 49, 125 (2012); https://doi.org/10.1002/jhet.782.
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R.P. Kagne, G.H. Nikam, V.G. Kalalawe, S.N. Niwadange and D.R. Munde, J. Chem. Chem. Sci, 7, 1064 (2017).
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B.P. Reddy, K. Rajesh and V. Vijayakumar, Arab. J. Chem., 8, 138 (2015); https://doi.org/10.1016/j.arabjc.2011.01.027.
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L. Deng, Q. Xu and H. Wu, Procedia Environ. Sci., 31, 662 (2016); https://doi.org/10.1016/j.proenv.2016.02.122.
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C. Liu, Z. Zhou, Y. Huang, Z. Cheng and W. Yuan, Chin. J. Chem. Eng., 22, 383 (2014); https://doi.org/10.1016/S1004-9541(14)60038-0.
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