Copyright (c) 2023 U. M. MANDLE, S. B. Rathod, N. S. KOLATE, P. A. NANAWARE, V. S. RANE, P. A. AMBLE, K. S. LOHAR, B. L. Shinde
This work is licensed under a Creative Commons Attribution 4.0 International License.
An Efficient One-Pot Synthesis of Octahydroquinazolinone Derivatives Using Magnetic Cobalt Ferrite Catalyst
Corresponding Author(s) : B. L. Shinde
Asian Journal of Chemistry,
Vol. 35 No. 9 (2023): Vol 35 Issue 9, 2023
Abstract
In this work, octahydroquinazolinone derivatives were synthesized using magnetic cobalt ferrite nanoparticles using oxalate precursor method. The XRD pattern and IR spectrum confirmed the formation of single segment cubic spinel cobalt ferrite. The average size of the crystallites was determined to be 26.599 nm, while the lattice constant was found to be 8.365 Å. A fine spherical CoFe2O4 particles with some quantity of aggregation may be observed within the SEM and TEM images. Nano spinel cobalt ferrite nanoparticles is a easily synthesized, non-toxic, less expensive, effortlessly magnetically recoverable and green catalyst for the synthesis of octahydroquinazolinone derivatives through the condensation of aromatic aldehydes with urea or thiourea and dimedone. The advantages of this technique are quick reaction time, ease of product isolation and high yields.
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References
A. Dömling and I. Ugi, Angew. Chem. Int. Ed., 39, 3168 (2000); https://doi.org/10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U
M. Poliakoff, J.M. Fitzpatrick, T.R. Farren and P.T. Anastas, Science, 297, 807 (2002); https://doi.org/10.1126/science.297.5582.807
J.D. Sunderhaus and S.F. Martin, Chem. Eur. J., 15, 1300 (2009); https://doi.org/10.1002/chem.200802140
R.C. Cioc, E. Ruijter and R.V. Orru, Green Chem., 16, 2958 (2014); https://doi.org/10.1039/C4GC00013G
S.S. van Berkel, B.G. Bögels, M.A. Wijdeven, B. Westermann and F.P. Rutjes, Eur. J. Org. Chem., 2012, 3543 (2012); https://doi.org/10.1002/ejoc.201200030
U.M. Mandle, A.M. Pachpinde, D.R. Kulkarni and B.L. Shinde, Mater. Today Proc., 46, 6122 (2021); https://doi.org/10.1016/j.matpr.2020.03.583
N. Kerru, L. Gummidi, S.N. Maddila, K.K. Gangu and S.B. Jonnalagadda, Inorg. Chem. Commun., 116, 107935 (2020); https://doi.org/10.1016/j.inoche.2020.107935
N. Bahlawane, P.H.T. Ngamou, V. Vannier, T. Kottke, J. Heberle and K. Kohse-Höinghaus, Phys. Chem. Chem. Phys., 11, 9224 (2009); https://doi.org/10.1039/b910707j
M. Houshiar, F. Zebhi, Z.J. Razi, A. Alidoust and Z. Askari, J. Magn. Magn. Mater., 371, 43 (2014); https://doi.org/10.1016/j.jmmm.2014.06.059
N.C. Desai, A. Dodiya and N. Shihory, J. Saudi Chem. Soc., 17, 259 (2013); https://doi.org/10.1016/j.jscs.2011.04.001
S.S. Chine, C.S. Patil and R.P. Pawar, Eur. Chem. Bull., 7, 318 (2019); https://doi.org/10.17628/ecb.2018.7.318-323
A. Mobinikhaledi, N. Foroughifar and H. Khodaei, Eur. J. Chem., 1, 291 (2010); https://doi.org/10.5155/eurjchem.1.4.291-293.108
P.V. Badadhe, A.V. Chate, D.G. Hingane, P.S. Mahajan, N.M. Chavhan and C.H. Gill, J. Korean Chem. Soc., 55, 936 (2011); https://doi.org/10.5012/jkcs.2011.55.6.936
Z. Hassani, M.R. Islami and M. Kalantari, Bioorg. Med. Chem. Lett., 16, 4479 (2006); https://doi.org/10.1016/j.bmcl.2006.06.038
I.S. Nosulenko, O.Y. Voskoboynik, G.G. Berest, S.L. Safronyuk, S.I. Kovalenko, O.M. Kamyshnyi and A.V. Katsev, Sci. Pharm., 82, 483 (2014); https://doi.org/10.3797/scipharm.1402-10
K. Nikoofar and Z. Khademi, Res. Chem. Intermed., 42, 3929 (2016); https://doi.org/10.1007/s11164-015-2260-6
P.M. Shah and M.P. Patel, Med. Chem. Res., 21, 1188 (2012); https://doi.org/10.1007/s00044-011-9628-y
S.Y. Srinivasan, K.M. Paknikar, D. Bodas and V. Gajbhiye, Nanomedicine, 13, 1221 (2018); https://doi.org/10.2217/nnm-2017-0379
G. Allaedini, S.M. Tasirin and P. Aminayi, Int. Nano Lett., 5, 183 (2015); https://doi.org/10.1007/s40089-015-0153-8
B.L. Shinde, U.M. Mandle, A.M. Pachpinde and K.S. Lohar, J. Therm. Anal. Calorim., 147, 2947 (2022); https://doi.org/10.1007/s10973-021-10719-0