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An Efficient and Green Synthesis of Benzylidene-2-N-(carbothioamido)-6-oxo-1,2,5,6-tetrahydro-1-NH-1,2,4-triazine Derivatives and their Antibacterial Activity Evaluation
Corresponding Author(s) : V. Anitha Rani
Asian Journal of Chemistry,
Vol. 26 No. 18 (2014): Vol 26 Issue 18
Abstract
An efficient and green synthesis of (Z)-3-allkyl-5(benzylidene/substituted benzylidene)-2N- (carbothioamido)-6-oxo-1,2,5,6-tetrahydro-1-NH-1,2,4-triazine derivatives have been developed in good yields and tested for their antibacterial activities against Escherichia coli, Providencia aeruginosa, Pseudomonas azotogensis and Baccilus subtillis. Some of the synthesized compounds possess good activity against Escherichia coli and Baccilus subtillis compared to standard drug streptomycin.
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References
M. Kidwai, Y. Goel and R. Kumar, Indian J. Chem., 37B, 174 (1998).
B.S. Holla, R. Gonsalves, B.S. Rao, S. Shenoy and H.N. Gopalakrishna, Farmaco, 56, 899 (2001); doi:10.1016/S0014-827X(01)01119-3.
R.M. Abdel- Rahman, J.M. Morsy, F. Hanafy and H.A. Amene, Pharmazie, 54, 347 (1999).
M.W. Partridge and M.F.G. Stevens, J. Chem. Soc. C, 1127 (1966); doi:10.1039/J39660001127.
Z.K. Abd El-Samii, J. Chem. Technol. Biotechnol, 53, 143 (1992); doi:10.1002/jctb.280530206.
M.P. Hay, F.B. Pruijn, S.A. Gamage, H.D.S. Liyanage, M.S. Kovacs, A.V. Patterson, W.R. Wilson, J.M. Brown and W.A. Denny, J. Med. Chem., 47, 475 (2004); doi:10.1021/jm030399c.
W.P. Heilman, R.D. Heilman, J.A. Scozzie, R.J. Wayner, J.M. Gullo and Z.S. Ariyan, J. Med. Chem., 22, 671 (1979); doi:10.1021/jm00192a012.
J.G. Erickson, Chem. Heterocycl. Compd., 10, 44 (1956).
R.L. Jones and J.R. Kershaw, Rev. Pure Appl. Chem, 21, 23 (1971).
G.J. Collee, G.A. Fraser, P.B. Marmion and A. Simmons, Practical Medical Microbiology, Churchill Livingstone: Edinburgh, edn 14, vol. 11, p. 163 (1996).
S.S. Tiwari and R.K. Satsangi, J. Indian Chem. Soc., 56, 627 (1979).
E.J. Budovskii, C. Chang, N. Kochetkov, Z. Obschchikim., 31, 1297 (1961).