Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

Efficient Synthesis of 4-Arylmethylene-3-methylisoxazol-5(4H)-one Derivatives Catalyzed by Malic Acid

Author(s): Sayed Zakaria Tahmasabi, Hamzeh Kiyani* and Heshmat Allah Samimi

Volume 20, Issue 2, 2023

Published on: 13 October, 2022

Page: [167 - 174] Pages: 8

DOI: 10.2174/1570178619666220903155012

Price: $65

Abstract

The efficient, straightforward, and green procedure was established in the direction of synthesis of 4-arylmethylene-3-methylisoxazol-5(4H)-one derivatives using the malic acid, which acted as the catalyst for the three-component heterocyclization reaction. In this reaction, aryl/heteroaryl aldehydes, hydroxylamine hydrochloride, and ethyl acetoacetate/ethyl benzoylacetate were applied as the reactants. The reaction was optimized to attain the best conditions for the synthesis of target heterocyclic compounds in a single step route. The best results were obtained from optimization experiments using 10 mol% malic acid as the catalyst, water solvent, and 50ºC temperature. The noticeable features of this process are the simplicity of the experimental procedure, the easy separation of the pure compounds from the product mixture, the simplicity of operation, avoidance of any hazardous organic solvents, no use of chromatographic purification techniques, clean reaction profiles, high yields, relatively short reaction time, and eco-friendliness.

Keywords: Aryl/heteroaryl aldehydes, Green conditions, Heterocyclization, Isoxazol-5(4H)-ones, Malic acid, Water.

Graphical Abstract

[1]
Arya, G.C.; Kaur, K.; Jaitak, V. Eur. J. Med. Chem., 2021, 221, 113511.
[http://dx.doi.org/10.1016/j.ejmech.2021.113511] [PMID: 34000484]
[2]
(a) Tang, D.; Iqbal, Z.; Sun, J.; Ji, J.; Yang, M.; Yang, Z. Tetrahedron Lett., 2021, 62, 152685. http://dx.doi.org/10.1016/j.tetlet.2020.152685;
(b) Li, L.; Huang, S.; Mao, K.; Lv, L.; Li, Z. Tetrahedron Lett., 2021, 71, 153052. http://dx.doi.org/10.1016/j.tetlet.2021.153052;
(c) Khodabandlou, S.; Saraei, M. Chem. Heterocycl. Compd., 2021, 57(7-8), 823-827.
[http://dx.doi.org/10.1007/s10593-021-02986-4]
[3]
Elqars, E.; Oubella, A.; Eddine Hachim, M.; Byadi, S.; Auhmani, A.; Guennoun, M.; Essadki, A.; Riahi, A.; Robert, A.; Youssef Ait Itto, M.; Nbigui, T. J. Mol. Liq., 2022, 347, 118311.
[http://dx.doi.org/10.1016/j.molliq.2021.118311]
[4]
Kamal, A.; Reddy, J.S.; Ramaiah, M.J.; Dastagiri, D.; Bharathi, E.V.; Azhar, M.A.; Sultana, F.; Pushpavalli, S.N.C.V.L. Eur. J. Med. Chem., 2010, 45, 3924-3937.
[http://dx.doi.org/10.1016/j.ejmech.2010.05.047] [PMID: 20557981]
[5]
Marwaha, S.; Uvell, H.; Salin, O.; Lindgren, A.E.G.; Silver, J.; Elofsson, M.; Gylfe, Å. Antimicrob. Agents Chemother., 2014, 58(5), 2968-2971.
[http://dx.doi.org/10.1128/AAC.02015-13] [PMID: 24566180]
[6]
Karetnikov, G.L.; Skvortsov, D.A.; Lopatukhina, E.V.; Nikolaeva, S.N.; Bondarenko, O.B. Asian J. Org. Chem., 2021, 10(12), 3343-3348.
[http://dx.doi.org/10.1002/ajoc.202100551]
[7]
Li, J.; Lin, Z.; Wu, W.; Jiang, H. Org. Chem. Front., 2020, 7(16), 2325-2348.
[http://dx.doi.org/10.1039/D0QO00609B]
[8]
Panda, S.S.; Chowdary, P.V.R.; Jayashree, B.S. Indian J. Pharm. Sci., 2009, 71(6), 684-687.
[http://dx.doi.org/10.4103/0250-474X.59554] [PMID: 20376225]
[9]
Agrawal, N.; Mishra, P. Med. Chem. Res., 2018, 27(5), 1309-1344.
[http://dx.doi.org/10.1007/s00044-018-2152-6] [PMID: 32214770]
[10]
Aret, E.; Meekes, H.; Vlieg, E.; Deroover, G. Dyes Pigments, 2007, 72(3), 339-344.
[http://dx.doi.org/10.1016/j.dyepig.2005.09.018]
[11]
Ghosh, T.; Gopal, A.; Saeki, A.; Seki, S.; Nair, V.C. Phys. Chem. Chem. Phys., 2015, 17(16), 10630-10639.
[http://dx.doi.org/10.1039/C5CP01044F] [PMID: 25805168]
[12]
Gao, M.; Zhang, J.; Zhang, X.; Xu, D.; Hu, Z.; Yao, J.; Wu, Y. Cryst. Growth Des., 2021, 21(6), 3153-3157.
[http://dx.doi.org/10.1021/acs.cgd.1c00221]
[13]
Wazalwar, S.S.; Banpurkar, A.R.; Perdih, F. J. Mol. Struct., 2017, 1150, 258-267.
[http://dx.doi.org/10.1016/j.molstruc.2017.08.094]
[14]
Kafle, B.; Cho, H.J. Bull. Korean Chem. Soc., 2012, 33(1), 275-277.
[http://dx.doi.org/10.5012/bkcs.2012.33.1.275]
[15]
Gulati, S. Sci. Rep., 2021, 11, 23563.
[http://dx.doi.org/10.1038/s41598-021-03057-6] [PMID: 34876634]
[16]
Kuchana, M.; Bethapudi, D.R.; Ediga, R.K.; Sisapuram, Y. J. Appl. Pharm. Sci., 2019, 9, 105-110.
[17]
Ishioka, T.; Kubo, A.; Koiso, Y.; Nagasawa, K.; Itai, A.; Hashimoto, Y. Bioorg. Med. Chem., 2002, 10(5), 1555-1566.
[http://dx.doi.org/10.1016/S0968-0896(01)00421-7] [PMID: 11886817]
[18]
Breuer, S.; Chang, M.W.; Yuan, J.; Torbett, B.E. J. Med. Chem., 2012, 55(11), 4968-4977.
[http://dx.doi.org/10.1021/jm201442t] [PMID: 22587465]
[19]
Anwar, T.; Nadeem, H.; Sarwar, S.; Naureen, H.; Ahmed, S.; Khan, A.; Arif, M. Drug Dev. Res., 2020, 81(7), 893-903.
[http://dx.doi.org/10.1002/ddr.21711] [PMID: 32662202]
[20]
Ali, M.; Saleem, U.; Anwar, F.; Imran, M.; Nadeem, H.; Ahmad, B.; Ali, T. Neurochem. Res., 2021, 46, 905-920.
[http://dx.doi.org/10.1007/s11064-021-03229-w] [PMID: 33486698]
[21]
Macchia, A.; Cuomo, V.D.; Di Mola, A.; Pierri, G.; Tedesco, C.; Palombi, L.; Massa, A. Eur. J. Org. Chem., 2020, 2020(15), 2264-2270.
[http://dx.doi.org/10.1002/ejoc.202000286]
[22]
Fernandes, A.A.G.; da Silva, A.F.; Okada, C.Y., Jr; Suzukawa, V.; Cormanich, R.A.; Jurberg, I.D. Eur. J. Org. Chem., 2019, 2019(19), 3022-3034.
[http://dx.doi.org/10.1002/ejoc.201900187]
[23]
Wannenmacher, N.; Pfeffer, C.; Frey, W.; Peters, R. J. Org. Chem., 2022, 87(1), 670-682.
[http://dx.doi.org/10.1021/acs.joc.1c02640] [PMID: 34890190]
[24]
Li, L.; Luo, P.; Deng, Y. Shao. Z. Angew. Chem. Int. Ed., 2019, 58(14), 4710-4713.
[http://dx.doi.org/10.1002/anie.201901511]
[25]
Niu, Q.; Xi, J.; Li, L.; Li, L.; Pan, C.; Lan, M.; Rong, L. Tetrahedron Lett., 2019, 60(43), 151181.
[http://dx.doi.org/10.1016/j.tetlet.2019.151181]
[26]
Ghogare, R.S.; Patankar-Jain, K. Lett. Org. Chem., 2021, 18, 83-87.
[http://dx.doi.org/10.2174/1570178617999200721011300]
[27]
Kalhor, M.; Samiei, S. Silicon, 2021, 13, 201-210.
[http://dx.doi.org/10.1007/s12633-020-00413-5]
[28]
Deshmukh, S.R.; Nalkar, A.S.; Thopate, S.R. J. Chem. Sci., 2022, 134(1), 15.
[http://dx.doi.org/10.1007/s12039-021-02016-y]
[29]
Basak, P.; Dey, S. ChemistrySelect, 2020, 5, 626-636.
[http://dx.doi.org/10.1002/slct.201904164]
[30]
Parveen, M.; Aslam, A.; Ahmad, A.; Alam, M.; Silva, M.R.; Silva, P.S.P. J. Mol. Struct., 2020, 1200, 127067.
[http://dx.doi.org/10.1016/j.molstruc.2019.127067]
[31]
Kasar, S.B.; Thopate, S.R. Curr. Organocatal., 2019, 6(3), 231-237.
[http://dx.doi.org/10.2174/2213337206666190411115402]
[32]
Mosallanezhad, A.; Kiyani, H. Curr. Organocatal., 2019, 6(1), 28-35.
[http://dx.doi.org/10.2174/2213337206666190214161332]
[33]
Farahi, S.; Nowrouzi, N. Iran. J. Sci. Technol. Trans. A Sci., 2018, 42, 1881-1887.
[http://dx.doi.org/10.1007/s40995-017-0453-0]
[34]
Ghorbani, F.; Kiyani, H.; Pourmousavi, S.A. Res. Chem. Intermed., 2020, 46(1), 943-959.
[http://dx.doi.org/10.1007/s11164-019-03999-7]
[35]
Ghorbani, F.; Kiyani, H. Res. Chem. Intermed., 2015, 41, 2653-2664.
[http://dx.doi.org/10.1007/s11164-013-1411-x]
[36]
Barkule, A.B.; Gadkari, Y.U.; Telvekar, V.N. Polycycl. Aromat. Compd., 2021, 1-12.
[http://dx.doi.org/10.1080/10406638.2021.1959353]
[37]
Faramarzi, Z.; Kiyani, H. Polycycl. Aromat. Compd., 2022, 1-23.
[http://dx.doi.org/10.1080/10406638.2022.2061533]
[38]
Faramarzi, Z.; Kiyani, H. Heterocycles, 2021, 102, 1779-1790.
[http://dx.doi.org/10.3987/COM-21-14488]
[39]
Kiyani, H.; Mosallanezhad, A. Curr. Org. Synth., 2018, 15(5), 715-722.
[http://dx.doi.org/10.2174/1570179415666180423150259]
[40]
Reihani, N.; Kiyani, H. Curr. Org. Chem., 2021, 25(8), 950-962.
[http://dx.doi.org/10.2174/1385272825666210212120517]
[41]
Damghani, F.K.; Kiyani, H.; Pourmousavi, S.A. Curr. Green Chem., 2020, 7(2), 217-225.
[http://dx.doi.org/10.2174/2213346107666200122093906]
[42]
Shanshak, M.; Budagumpi, S. Małecki, J.G.; Keri, R.S. Appl. Organomet. Chem., 2020, 44, e5544.
[43]
Kadam, H.K.; Salkar, K.; Naik, A.P.; Naik, M.M.; Salgaonkar, L.N.; Charya, L.; Pinto, K.C. ChemistrySelect, 2021, 6, 11718-11728.
[http://dx.doi.org/10.1002/slct.202101798]
[44]
Kiyani, H.; Kanaani, A.; Ajloo, D.; Ghorbani, F.; Vakili, M. Res. Chem. Intermed., 2015, 41(10), 7739-7773.
[http://dx.doi.org/10.1007/s11164-014-1857-5]
[45]
Kiyani, H.; Ghorbani, F. Res. Chem. Intermed., 2015, 41(10), 7847-7882.
[http://dx.doi.org/10.1007/s11164-014-1863-7]
[46]
Kiyani, H.; Jabbari, M.; Mosallanezhad, A. J. Chem., 2014, 9, 279-289.
[47]
Kiyani, H.; Darbandi, H.; Mosallanezhad, A.; Ghorbani, F. Res. Chem. Intermed., 2015, 41(10), 7561-7579.
[http://dx.doi.org/10.1007/s11164-014-1844-x]
[48]
Kiyani, H.; Ghorbani, F. J. Saudi Chem. Soc., 2017, 21, S112-S119.
[http://dx.doi.org/10.1016/j.jscs.2013.11.002]
[49]
Mosallanezhad, A.; Kiyani, H. Electron. J. Chem., 2018, 10, 133-139.
[50]
Kiyani, H.; Ghorbani, F. Res. Chem. Intermed., 2016, 42(9), 6831-6844.
[http://dx.doi.org/10.1007/s11164-016-2498-7]
[51]
Kiyani, H.; Samimi, H.A. Warasan Khana Witthayasat Maha Witthayalai Chiang Mai, 2017, 44, 1011-1021.
[52]
(a) Patil, B.M.; Shinde, S.K.; Jagdale, A.A.; Jadhav, S.D.; Patil, S.S. Res. Chem. Intermed., 2021, 47(10), 4369-4398.
[http://dx.doi.org/10.1007/s11164-021-04539-y];
(b) Popatkar, B.B.; Mane, A.A.; Meshram, G.A. Indian J. Chem., 2021, 60B, 1362-1367.;
(c) Kadu, V.R.; Gholap, S.S. Indian J. Heterocycl. Chem., 2019, 29, 319-326.;
d) Vekariya, R.H.; Patel, K.D.; Patel, H.D. Res. Chem. Intermed., 2016, 42(10), 7559-7579.
[http://dx.doi.org/10.1007/s11164-016-2553-4]
[53]
Kaminwar, N.S.; Tekale, S.U.; Nakkalwar, S.L.; Pawar, R.P. Lett. Org. Chem., 2021, 18(12), 945-949.
[http://dx.doi.org/10.2174/1570178618666210729114845]
[54]
Gharehassanlou, S.; Kiyani, H. Indian J. Chem., 2022, 61, 515-520.
[55]
(a) Kiyani, H.; Tazari, M.; Ghorbani, F. Lett. Org. Chem., 2018, 15, 523-529.;
(b) Kiyani, H. Curr. Org. Synth., 2018, 15, 1043-1072.;
(c) Tazari, M.; Kiyani, H. Curr. Org. Synth., 2019, 16, 793-800.;
d) Tazari, M.; Kiyani, H. Res. Chem. Intermed., 2017, 43, 6639-6650.;
e) Zhu, F.X.; Wang, W.; Li, H.X. J. Am. Chem. Soc., 2011, 133, 11632-11640.;
f) Candeias, N.R.; Cal, P.M.S.D.; Andre, V.; Duarte, M.T.; Veiros, L.F.; Gois, P.M.P. Tetrahedron, 2010, 66, 2736-2745.
[56]
Kar, S.; Sanderson, H.; Roy, K.; Benfenati, E. Leszczynski. J. Chem. Rev., 2022, 122(3), 3637-3710.
[http://dx.doi.org/10.1021/acs.chemrev.1c00631] [PMID: 34910451]
[57]
Knesebeck, A.M.; Ortiz, R.W.P.; Wypych, F.; Zanoelo, E.F. Ind. Eng. Chem. Res., 2019, 58, 9257-9265.
[http://dx.doi.org/10.1021/acs.iecr.9b00583]
[58]
Liu, J.; Du, Z.; Yang, Y.; Lu, T.; Lu, F.; Xu, J. ChemSusChem, 2012, 5(11), 2151-2154.
[http://dx.doi.org/10.1002/cssc.201200489] [PMID: 23055457]
[59]
Ortiz, R.W.P.; de Jesús, B.G.; Franceschi, E.; Dariva, C.; Cardozo-Filho, L.; Zanoelo, E.F. React. Kinet. Mech. Catal., 2017, 122(2), 793-802.
[http://dx.doi.org/10.1007/s11144-017-1287-7]
[60]
Zou, X.; Zhou, Y.; Yang, S.T. Biotechnol. Bioeng., 2013, 110(8), 2105-2113.
[http://dx.doi.org/10.1002/bit.24876] [PMID: 23436475]
[61]
Sandeep, K.B.; Shankar, T.R. Curr. Green Chem., 2018, 5, 177-184.
[http://dx.doi.org/10.2174/2213346105666180821114459]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy