European Journal of Chemistry

A new facile and efficient synthesis of 2-((5-aryl-1,3,4-oxadiazol-2-yl) methoxy)-3-methyl quinoxaline and 3-methylquinoxalin-2-yl-2-(5-aryl-2H-tetrazol-2-yl)acetate derivatives



Main Article Content

Shashikala Kethireddy
Hemalatha Kotakommula
Laxminarayana Eppakayala
Thirumala Chary Mariganti

Abstract

Newly synthesized compounds containing quinoxaline ring fused with tetrazoles and oxadiazoles show array of pharmacological activities, especially, anti-inflammatory, analgesic and anticonvulsant activities. The ability to serve as surrogates or bioisosteres for carboxylic acids, esters and carboxamides made them important moieties in drug designing. Considering the importance of quinoxalines, tetrazoles and 1,3,4-oxadiazoles to both medicinal and heterocyclic chemistry, the following 2-((5-aryl-1,3,4-oxadiazol-2-yl)methoxy)-3-methyl quinoxaline and 3-methylquinoxalin-2-yl-2-(5-aryl-2H-tetrazol-2-yl)acetate derivatives are synthesized. The structures of the synthesized compounds were confirmed by 1H NMR, 13C NMR and Mass spectral data. All the synthesized derivatives were tested in vitro for their antibacterial activity.


icon graph This Abstract was viewed 1612 times | icon graph Article PDF downloaded 795 times

How to Cite
(1)
Kethireddy, S.; Kotakommula, H.; Eppakayala, L.; Mariganti, T. C. A New Facile and Efficient Synthesis of 2-(5-Aryl-1,3,4-Oxadiazol-2-Yl) Methoxy)-3-Methyl Quinoxaline and 3-Methylquinoxalin-2-Yl-2-(5-Aryl-2H-Tetrazol-2-yl)acetate Derivatives. Eur. J. Chem. 2017, 8, 125-129.

Article Details

Share
Crossref - Scopus - Google - European PMC
References

[1]. Bekhit, A. A.; El-Sayed, O. A.; El-Sayedi, A.; Park, J. Y. Eur. J. Med. Chem. 2004, 39, 249-255.
https://doi.org/10.1016/j.ejmech.2003.12.005

[2]. Smita, S.; Sharma, M. C.; Kohli, D. V. J. Optoelect. Biomed. Mat. 2010, 1(3), 151-160.

[3]. Mohite, P. B.; Bhaskar, V. H. Int. J. Pharm. Tech. Res. 2011, 3, 1557-1566.

[4]. Wagle, S.; Adhikari, A. V.; Kumari, S. K. Eur. J. Med. Chem. 2009, 44, 1135-1143.
https://doi.org/10.1016/j.ejmech.2008.06.006

[5]. Upadhayaya, R. S.; Jain, S.; Sinha, N.; Kishore, N.; Chandra, R.; Arora, S. K. Eur. J. Med. Chem. 2004, 39, 579-592.
https://doi.org/10.1016/j.ejmech.2004.03.004

[6]. Matysiak, J.; Niewiadomy, A.; Krajewska-Kulak, E.; Niewiadomy, M. G. Il Farmaco 2003, 58, 455-461.
https://doi.org/10.1016/S0014-827X(03)00046-6

[7]. Popat, B. M.; Vaidhun, H. B. Orbital-Elec. J. Chem. 2010, 3, 311-315.

[8]. Rajasekaran, A.; Thampi, P. P. Eur. J. Med. Chem. 2004, 39, 273-279.
https://doi.org/10.1016/j.ejmech.2003.11.016

[9]. Rajasekaran, A.; Thampi, P. P. Eur. J. Med. Chem. 2005, 40, 1359-1364.
https://doi.org/10.1016/j.ejmech.2005.07.013

[10]. Bhaskar, V. H.; Mohite, P. B. J. Optoelect. Biomed. Mat. 2010, 2(4), 249-259.

[11]. Pattan, S. R.; Kekare, P.; Patil, A.; Nikalge, A.; Kittur, B. S. Iran J. Pharm. Sci. 2009, 5(4), 225-230.

[12]. Basheer, H. A.; Aveen, A. I.; Maysoon, S. A. J. Pure Appl. Chem. 2016, 2(1), 1-3.

[13]. Navidpour, L.; Amini, M.; Shafaroodi, H.; Abdi, K.; Ghahremani, M. H.; Dehpour, A. R.; Shafiee, A. Bioorg. Med. Chem. Lett. 2006, 15, 4483-4487.
https://doi.org/10.1016/j.bmcl.2006.06.032

[14]. Gao, Y. L.; Zhao, G. L.; Liu, W.; Shao, H.; Wang, Y. L.; Xu, W. R.; Tangand, L. D.; Wang, J. W. Indian J. Chem. B 2010, 49, 1499-1508.

[15]. Rajasekaran, A.; Rajagopal, K. A. Acta Pharm. 2009, 59, 355-364.
https://doi.org/10.2478/v10007-009-0026-7

[16]. Gundugola, A. S.; Chandra, K. L.; Perchellet, E. M.; Water, A. M.; Rayat, S. Bioorg. Med. Chem. Lett. 2010, 20, 3920-3924.
https://doi.org/10.1016/j.bmcl.2010.05.012

[17]. Sharon, A.; Pratap, R.; Tiwari, P.; Srivastava, A.; Maulik, P. R.; Vishnu, J. R. Bioorg. Med. Chem. Lett. 2005, 15, 2115-2117.
https://doi.org/10.1016/j.bmcl.2005.02.060

[18]. Umarani, N.; Kaliappan, I.; Singh, N. K. Derpharma Chem. 2010, 2(1), 159-167.

[19]. Umarani, N. K. Int. J. Pharm. Sci. Rev. Res. 2010, 2(2), 24-28.

[20]. Othman, A. A.; Mebrouk, K.; Sarah, A. Arab. J. Chem. 2014, 32, 714-725.

[21]. Oliveira, C. S.; Lira, B. F.; Barbosa-Filho, J. M.; Lorenzo, J. G. F.; Athayde-Filho, P. F. Molecules 2012, 17, 10192-10231.
https://doi.org/10.3390/molecules170910192

Supporting Agencies

Geethanjali College of Engineering and Technology, Keesara, Rangareddy, 501301, Telangana, India
Most read articles by the same author(s)

Most read articles by the same author(s)

TrendMD

Dimensions - Altmetric - scite_ - PlumX

Downloads and views

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...
License Terms

License Terms

by-nc

Copyright © 2024 by Authors. This work is published and licensed by Atlanta Publishing House LLC, Atlanta, GA, USA. The full terms of this license are available at https://www.eurjchem.com/index.php/eurjchem/terms and incorporate the Creative Commons Attribution-Non Commercial (CC BY NC) (International, v4.0) License (http://creativecommons.org/licenses/by-nc/4.0). By accessing the work, you hereby accept the Terms. This is an open access article distributed under the terms and conditions of the CC BY NC License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited without any further permission from Atlanta Publishing House LLC (European Journal of Chemistry). No use, distribution, or reproduction is permitted which does not comply with these terms. Permissions for commercial use of this work beyond the scope of the License (https://www.eurjchem.com/index.php/eurjchem/terms) are administered by Atlanta Publishing House LLC (European Journal of Chemistry).