Copyright (c) 2021 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Antimicrobial Activity of Cyclic Dithiocarbamates Employing Triton-B/CS2 System
Corresponding Author(s) : Sangeeta Bajpai
Asian Journal of Chemistry,
Vol. 33 No. 5 (2021): Vol 33 Issue 5, 2021
Abstract
An efficient and green methodology to synthesize cyclic dithiocarbamates (compounds 1-11) was developed by reaction of primary amines, CS2 and 1,2-dibromoethane or 1,4-dibromobutane, catalyzed by Triton-B (as PTC)/CS2 system. Mass spectroscopy, elemental analysis and 1H NMR are used for characterization of the synthesized compounds (1-11). This effectual green tactics give good yield of product which entails mild conditions. Compounds (1-11) were found to possess in vitro antimicrobial activities against the pathogenic bacterial and fungal strain. The microbial strains used to screen activities are Escherichia coli, Staphylococcus aureus and Candida albicans.
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- S.L. Cao, Y. Han, C.Z. Yuan, Y. Wang, J.K. Xiahou, J. Liao, R.T. Gao, B.B. Mao, B.L. Zhao, J.F. Li and X. Xu, Eur. J. Med. Chem., 64, 401 (2013); https://doi.org/10.1016/j.ejmech.2013.04.017
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N.C. Desai, K. Rajpara and V.V. Joshi, J. Fluor. Chem., 145, 102 (2013); https://doi.org/10.1016/j.jfluchem.2012.10.012
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R.S. Grainger and P. Innocenti, Heteroatom Chem., 18, 568 (2007); https://doi.org/10.1002/hc.20336
N. Alexander, K. Ramalingam and C. Rizzoli, Inorg. Chim. Acta, 365, 480 (2011); https://doi.org/10.1016/j.ica.2010.09.029
P. Liu, C. Li, J. Zhang and X. Xu, Synth. Commun., 43, 3342 (2013); https://doi.org/10.1080/00397911.2013.783600
A.Z. Halimehjani, Y. Pourshojaei and M.R. Saidi, Tetrahedron Lett., 50, 32 (2009); https://doi.org/10.1016/j.tetlet.2008.10.063
L. Jamir, U.B. Sinha, J. Nath and B.K. Patel, Synth. Commun., 42, 951 (2012); https://doi.org/10.1080/00397911.2010.532276
M. Kienle, A. Unsinn and P. Knochel, Angew. Chem. Int. Ed., 49, 4751 (2010); https://doi.org/10.1002/anie.201001025
V. Aucagne, C. Lorin, A. Tatibouet and P. Rollin, Tetrahedron Lett., 46, 4349 (2005); https://doi.org/10.1016/j.tetlet.2005.04.112
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L.J. Bahrin, P.J. Jones and H. Hopf, Beilstein J. Org. Chem., 8, 1999 (2012); https://doi.org/10.3762/bjoc.8.226
P.M. Madalageri and O. Kotresh, J. Chem. Pharm. Res., 4, 2697 (2012).
K. Bacharaju, S.R. Jambula, S. Sivan, S. Jyostnatangeda and V. Manga, Bioorg. Med. Chem. Lett., 22, 3274 (2012); https://doi.org/10.1016/j.bmcl.2012.03.018
D. Chaturvedi, A. Kumar and S. Ray, Synth. Commun., 32, 2651 (2002); https://doi.org/10.1081/SCC-120006028
D. Chaturvedi, A. Kumar and S. Ray, Tetrahedron Lett., 44, 7637 (2003); https://doi.org/10.1016/j.tetlet.2003.08.018
D. Chaturvedi and S. Ray, Lett. Org. Chem., 2, 742 (2005); https://doi.org/10.2174/157017805774717472
D. Chaturvedi and S. Ray, J. Sulfur Chem., 26, 365 (2005); https://doi.org/10.1080/17415990500404848
D. Chaturvedi and S. Ray, J. Sulfur Chem., 27, 265 (2006); https://doi.org/10.1080/17415990600701697
R. Kishore, M. Kamboj, M. Shukla and N. Srivastava, Asian J. Chem., 31, 1091 (2019); https://doi.org/10.14233/ajchem.2019.21830
S. Zaidi, A.K. Chaturvedi, N. Singh and D. Chaturvedi, Curr. Chem. Lett., 6, 143 (2017); https://doi.org/10.5267/j.ccl.2017.7.001