Copyright (c) 2016 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Synthesis and Antibacterial Studies of 1-[3-(Trifluoromethoxy)phenylmethanone]piperidine-4-carboxylic Acid Derivatives
Corresponding Author(s) : P. Venkataramana
Asian Journal of Chemistry,
Vol. 28 No. 1 (2016): Vol 28 Issue 1
Abstract
Synthesis of novel piperidine-4-carboxamide derivatives as antibacterial agents has elevated impact on medicinal field. In the present work, ten new compounds were synthesized and screened toward their antibacterial studies. The structures of these compounds were characterized and analyzed by spectral studies such as IR, mass and 1H NMR and compounds 6a and 6c-6h, were observed to possess potent antimicrobial activity.
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- M.G.P. Buffat, Tetrahedron, 60, 1701 (2004); doi:10.1016/j.tet.2003.11.043.
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- P.M. Weintraub, J.S. Sabol, J.M. Kane and D.R. Borcherding, Tetrahedron, 59, 2953 (2003); doi:10.1016/S0040-4020(03)00295-3.
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- V.B.P. Reddy, P. Prasad and P. Venkataramana, J. Applicable Chem., 2, 1501 (2013).
References
M.G.P. Buffat, Tetrahedron, 60, 1701 (2004); doi:10.1016/j.tet.2003.11.043.
I. Ojima and D.M. Iula, in ed.: S.W. Pelletier, Chemical and Biological Perspectives, Elsevier Science Ltd, UK, edn 13, pp. 371-410 (1999).
P.M. Weintraub, J.S. Sabol, J.M. Kane and D.R. Borcherding, Tetrahedron, 59, 2953 (2003); doi:10.1016/S0040-4020(03)00295-3.
Z. Dang, Y. Yang, R. Ji and S. Zhang, Bioorg. Med. Chem. Lett., 17, 4523 (2007); doi:10.1016/j.bmcl.2007.05.093.
H.-N. Shin, S.H. Seo, H. Choo, G. Kuem, K.I. Choi and G. Nam, Bioorg. Med. Chem. Lett., 23, 1193 (2013); doi:10.1016/j.bmcl.2013.01.033.
C.L. Cavallaro, S. Briceno, J. Chen, M.E. Cvijic, P. Davies, J. Hynes Jr., R.-Q. Liu, S. Mandlekar, A.V. Rose, A.J. Tebben, K. Van Kirk, A. Watson, H. Wu, G. Yang and P.H. Carter, J. Med. Chem., 55, 9643 (2012); doi:10.1021/jm300896d.
H. Khalid, Aziz-ur-Rehman, K.M. Khan, Int. J. Pharm. Pharmaceut. Sci., 4, 443 (2012).
S.P. Kalpesh and P.V. Sandip, Der Chemica Sinica, 3, 430 (2012).
M.K. Prashanth, H.D. Revanasiddappa, K.M. Lokanatha Rai and B. Veeresh, Bioorg. Med. Chem. Lett., 22, 7065 (2012); doi:10.1016/j.bmcl.2012.09.089.
Y.-Y. Zheng, L. Guo, X.-C. Zhen and J.-Q. Li, Eur. J. Med. Chem., 54, 123 (2012); doi:10.1016/j.ejmech.2012.04.030.
B.J. Mavunkel, J.J. Perumattam, X. Tan, G.R. Luedtke, Q. Lu, D. Lim, D. Kizer, S. Dugar, S. Chakravarty, Y. Xu, J. Jung, A. Liclican, D.E. Levy and J. Tabora, Bioorg. Med. Chem. Lett., 20, 1059 (2010); doi:10.1016/j.bmcl.2009.12.031.
X. Chen, P. Zhan, X. Liu, Z. Cheng, C. Meng, S. Shao, C. Pannecouque, E. De Clercq and X. Liu, Bioorg. Med. Chem., 20, 3856 (2012); doi:10.1016/j.bmc.2012.04.030.
X. Chen, P. Zhan, C. Pannecouque, J. Balzarini, E. De Clercq and X.Liu, Eur. J. Med. Chem., 51, 60 (2012); doi:10.1016/j.ejmech.2012.02.019.
S. Watanuki, K. Matsuura, Y. Tomura, M. Okada, T. Okazaki, M. Ohta and S. Tsukamoto, Bioorg. Med. Chem., 19, 5628 (2011); doi:10.1016/j.bmc.2011.07.030.
X.-H. Liu, J. Li, J.B. Shi, B.-A. Song and X.-B. Qi, Eur. J. Med. Chem., 51, 294 (2012); doi:10.1016/j.ejmech.2012.02.040.
V.B.P. Reddy, P. Prasad and P. Venkataramana, J. Applicable Chem., 2, 1501 (2013).