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Letters in Organic Chemistry

Editor-in-Chief

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

Research Article

Novel Approach for the Synthesis of 2, 5-disubstituted 1, 3, 4-thiadiazoles from Benzothiohydrazides and Ethylbenzimidate

Author(s): Shobha S, Kemparajegowda, Swamy Savvemala Girimanchanaika, Hassan A. Swarup and Kempegowda Mantelingu*

Volume 20, Issue 11, 2023

Published on: 22 June, 2023

Page: [1070 - 1076] Pages: 7

DOI: 10.2174/1570178620666230602085830

Price: $65

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Abstract

In the current study, a simple and reliable technique for the synthesis of 2,5-disubstituted 1,3,4-thiadiazoles from ethylbenzimidate and benzothiohydrazides were devised. This protocol goes via a base-mediated nucleophilic addition elimination process, followed by intramolecular rearrangement. Our method utilizes commonly accessible and non-toxic substrates and a simple workup procedure to produce high to exceptional yields (70-91%) of 2,5-diphenyl 1,3,4-thiadiazoles derivatives with a wide range of substitutions. We present a simple procedure for the synthesis of 1, 3, 4- thiadiazole using ethylbenzimidate and benzothiohydrazides in the presence of Et3N in DMSO solvent as affordable and easily accessible starting materials to create derivatives under ambient conditions.

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[1]
Wu, Z.; Shi, J.; Chen, J.; Hu, D.; Song, B. J. Agric. Food Chem., 2021, 69(31), 8660-8670.
[http://dx.doi.org/10.1021/acs.jafc.1c01626] [PMID: 34319116]
[2]
Khrustalev, V.N.; Grishina, M.M.; Matsulevich, Z.V.; Lukiyanova, J.M.; Borisova, G.N.; Osmanov, V.K.; Novikov, A.S.; Kirichuk, A.A.; Borisov, A.V.; Solari, E.; Tskhovrebov, A.G. Dalton Trans., 2021, 50(31), 10689-10691.
[http://dx.doi.org/10.1039/D1DT01322J] [PMID: 34165455]
[3]
Grudova, M.V.; Kubasov, A.S.; Khrustalev, V.N.; Novikov, A.S.; Kritchenkov, A.S.; Nenajdenko, V.G.; Borisov, A.V.; Tskhovrebov, A.G. Molecules, 2022, 27(3), 1029.
[http://dx.doi.org/10.3390/molecules27031029] [PMID: 35164294]
[4]
Gummidi, L.; Kerru, N.; Ebenezer, O.; Awolade, P.; Sanni, O.; Islam, M.S.; Singh, P. Bioorg. Chem., 2021, 115(May)105210
[http://dx.doi.org/10.1016/j.bioorg.2021.105210] [PMID: 34332231]
[5]
Jatav, V.; Mishra, P.; Kashaw, S.; Stables, J.P. Eur. J. Med. Chem., 2008, 43(9), 1945-1954.
[http://dx.doi.org/10.1016/j.ejmech.2007.12.003] [PMID: 18222569]
[6]
Chai, L.; Lai, Z.; Xia, Q.; Yuan, J.; Bian, Q.; Yu, M.; Zhang, W.; Xu, Y.; Xu, H. Eur. J. Org. Chem., 2018, 2018(31), 4338-4344.
[http://dx.doi.org/10.1002/ejoc.201800670]
[7]
Khan, I.; Ali, S.; Hameed, S.; Rama, N.H.; Hussain, M.T.; Wadood, A.; Uddin, R.; Ul-Haq, Z.; Khan, A.; Ali, S.; Choudhary, M.I. Eur. J. Med. Chem., 2010, 45(11), 5200-5207.
[http://dx.doi.org/10.1016/j.ejmech.2010.08.034] [PMID: 20828889]
[8]
Rzeski, W.; Matysiak, J. Kandefer-Szerszeń. M. Bioorg. Med. Chem., 2007, 15(9), 3201-3207.
[http://dx.doi.org/10.1016/j.bmc.2007.02.041] [PMID: 17350846]
[9]
Hu, Y.; Li, C.Y.; Wang, X.M.; Yang, Y.H.; Zhu, H.L. Chem. Rev., 2014, 114(10), 5572-5610.
[http://dx.doi.org/10.1021/cr400131u] [PMID: 24716666]
[10]
Peng, X.; Gao, H.; Xiao, Y.; Cheng, H.; Huang, F.; Cheng, X. New J. Chem., 2017, 41(5), 2004-2012.
[http://dx.doi.org/10.1039/C6NJ02604D]
[11]
Jain, A.K.; Sharma, S.; Vaidya, A.; Ravichandran, V.; Agrawal, R.K. Chem. Biol. Drug Des., 2013, 81(5), 557-576.
[http://dx.doi.org/10.1111/cbdd.12125] [PMID: 23452185]
[12]
Sharma, B.; Verma, A.; Sharma, U.K.; Prajapati, S. Med. Chem. Res., 2014, 23(1), 146-157.
[http://dx.doi.org/10.1007/s00044-013-0618-0]
[13]
Polshettiwar, V.; Varma, R.S. Tetrahedron Lett., 2008, 49(5), 879-883.
[http://dx.doi.org/10.1016/j.tetlet.2007.11.165]
[14]
Swamy, S.N. Basappa; Priya, B.S.; Prabhuswamy, B.; Doreswamy, B.H.; Prasad, J.S.; Rangappa, K.S. Eur. J. Med. Chem., 2006, 41(4), 531-538.
[http://dx.doi.org/10.1016/j.ejmech.2005.12.009] [PMID: 16529848]
[15]
Janowska, S.; Paneth, A.; Wujec, M. Molecules, 2020, 25(18), 4309.
[http://dx.doi.org/10.3390/molecules25184309] [PMID: 32962192]
[16]
Palaska, E. Şahin, G.; Kelicen, P.; Durlu, N.T.; Altinok, G. Farmaco, 2002, 57(2), 101-107.
[http://dx.doi.org/10.1016/S0014-827X(01)01176-4] [PMID: 11902651]
[17]
Ankali, K.N.; Rangaswamy, J.; Shalavadi, M.; Naik, N.; Krishnamurthy, G. J. Mol. Struct., 2021, 1236130357
[http://dx.doi.org/10.1016/j.molstruc.2021.130357]
[18]
Li, Y.J.; Sun, Y.Z.; Xu, Y.T.; Jin, K.; Wen, L.P.; Hou, N.B.; Sun, X.X. Chin. Chem. Lett., 2007, 18(9), 1047-1048.
[http://dx.doi.org/10.1016/j.cclet.2007.05.049]
[19]
Zarei, M. Tetrahedron, 2017, 73(14), 1867-1872.
[http://dx.doi.org/10.1016/j.tet.2017.02.042]
[20]
Fan, X.Y.; Jiang, X.; Zhang, Y.; Chen, Z.B.; Zhu, Y.M. Org. Biomol. Chem., 2015, 13(41), 10402-10408.
[http://dx.doi.org/10.1039/C5OB01328C] [PMID: 26328529]
[21]
Zhou, Z.; Liu, Y.; Chen, J.; Yao, E. Cheng. J. Org. Lett., 2016, 18(20), 5268-5271.
[http://dx.doi.org/10.1021/acs.orglett.6b02583] [PMID: 27684432]
[22]
Nandeesh, K.N.; Swarup, H.A.; Sandhya, N.C.; Mohan, C.D.; Pavan Kumar, C.S.; Kumara, M.N.; Mantelingu, K.; Ananda, S.; Rangappa, K.S. New J. Chem., 2016, 40(3), 2823-2828.
[http://dx.doi.org/10.1039/C5NJ02925B]
[23]
Sharma, S.; Varsha, K.K.; Kumari, S.; Gopalakrishnan, V.; Jose, A.E.; Choudhary, B.; Mantelingu, K.; Raghavan, S.C. Sci. Rep., 2020, 10(1), 15188.
[http://dx.doi.org/10.1038/s41598-020-72058-8] [PMID: 32938954]
[24]
Ray, U.; Mantelingu, K.; Raghavan, S.C.; Rangappa, K.S.; Rangappa, K.S. Russ. J. Bioorganic Chem., 2020, 46(5), 837-844.
[http://dx.doi.org/10.1134/S106816202005009X]
[25]
Hegde, M.; Mantelingu, K.; Swarup, H.A.; Pavankumar, C.S.; Qamar, I.; Raghavan, S.C.; Rangappa, K.S. RSC Advances, 2016, 6(8), 6308-6319.
[http://dx.doi.org/10.1039/C5RA19150E]
[26]
Ray, U.; Raul, S.K.; Gopinatha, V.K.; Ghosh, D.; Rangappa, K.S.; Mantelingu, K.; Raghavan, S.C. Mol. Carcinog., 2020, 59(6), 618-628.
[http://dx.doi.org/10.1002/mc.23186] [PMID: 32189406]
[27]
Hegde, M.; Mantelingu, K.; Pandey, M.; Pavankumar, C.S.; Rangappa, K.S.; Raghavan, S.C. Target. Oncol., 2016, 11(5), 655-665.
[http://dx.doi.org/10.1007/s11523-016-0441-x] [PMID: 27188390]
[28]
Sandhya, N.C.; Nandeesh, K.N.; Rangappa, K.S.; Ananda, S. RSC Advances, 2015, 5(38), 29939-29946.
[http://dx.doi.org/10.1039/C5RA02114F]
[29]
Ramesha, A.B.; Sandhya, N.C.; Pavan Kumar, C.S.; Hiremath, M.; Mantelingu, K.; Rangappa, K.S. New J. Chem., 2016, 40(9), 7637-7642.
[http://dx.doi.org/10.1039/C6NJ01038E]
[30]
Swarup, H.A.; Chaithra, N.; Mantelingu, K.; Rangappa, K.S. ChemistrySelect, 2018, 3(19), 5390-5394.
[http://dx.doi.org/10.1002/slct.201800886]
[31]
Ramesha, A.B.; Pavan Kumar, C.S.; Sandhya, N.C.; Kumara, M.N.; Mantelingu, K.; Rangappa, K.S. RSC Advances, 2016, 6(54), 48375-48378.
[http://dx.doi.org/10.1039/C6RA03771B]
[32]
Saegusa, Y.; Akano, N.; Nakamura, S.; Chau, N.; Iwakura, Y. Journal of polymer science. Part A-1. Polym. Chem., 1985, 23(11), 2727-2738.
[http://dx.doi.org/10.1002/pol.1985.170231101]
[33]
Avadhani, A.; Iniyavan, P.; Kumar, Y.; Ila, H. J. Org. Chem., 2021, 86(12), 8508-8515.
[http://dx.doi.org/10.1021/acs.joc.1c00616] [PMID: 34107686]
[34]
Thakur, R.; Jaiswal, Y.; Kumar, A. Org. Biomol. Chem., 2019, 17(46), 9829-9843.
[http://dx.doi.org/10.1039/C9OB01899A] [PMID: 31720673]
[35]
Gowda, K.; Swarup, H.A.; Nagarakere, S.C.; Rangappa, S.; Kanchugarkoppal, R.S.; Kempegowda, M. Synth. Commun., 2020, 50(10), 1528-1544.
[http://dx.doi.org/10.1080/00397911.2020.1745843]

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