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Synthesis and Herbicidal Activity of Amide Derivatives Containing Thiazole Moiety
Corresponding Author(s) : Jian-Quan Weng
Asian Journal of Chemistry,
Vol. 25 No. 4 (2013): Vol 25 Issue 4
Abstract
Twelve novel amide derivatives containing thiazole moiety were synthesized via a coupling reaction of [4-(substituted phenyl)thiazol-2-yl] acetonitrile and aryl isocyanates catalyzed by organic bases. Their structures were characterized by 1H NMR, FTIR, MS and elemental analysis. The preliminary bioassay indicated that these compounds exhibited moderate herbicidal activities against Echinochloa crusgalli and Amaranthus ascedense.
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- X.H. Liu, Y.X. Shi, Y. Ma, C.Y. Zhang, W.L. Dong, P. Li, B.L. Wang, B.J. Li and Z.M. Li, Eur. J. Med. Chem., 44, 2782 (2009).
- Y. Sawada, T. Yanai and H. Nakagawa, Pest Manage. Sci., 59, 49 (2003).
- J.Q. Weng, D.L. Shen, C.X. Tan and X.M. Ou, Chin. J. Org. Chem., 26, 1106 (2006).
- W.L. Dong, Z.X. Liu, X.H. Liu, Z.M. Li and W.G. Zhao, Eur. J. Med. Chem., 45, 1919 (2010).
- Z.Z. Zhou, Q. Chen and G.F. Yang, Chin. J. Org. Chem., 28, 1385 (2008).
- N. Muhammad, N. Muhammad, B. Iftikhar and R. Salma, J. Chem. Soc. Pak., 30, 780 (2008).
- W. Wang, G.P. Zhang, B.A. Song, H. Wang, L.H. Jin, D.Y. Hu and S. Yang, Chin. J. Org. Chem., 27, 279 (2007).
- Q.M. Wang, H. Li, Y.H. Li and R.Q. Huang, J. Agric. Food Chem., 52, 1918 (2004).
- P.C. David, V.E. Roy and T.H. Roy, J. Agric. Food Chem., 29, 640 (1981).
- R.E. Menzer and J.E. Casida, J. Agric. Food Chem., 13, 102 (1965).
- X.H. Liu, C.X. Tan and J.Q. Weng, Phosphorus Sulfur Silicon Rel. Elem., 186, 552 (2011).
- S. Vishnoi, V. Agrawal and V.K. Kasana, J. Agric. Food Chem., 57, 3261 (2009).
- J.Q. Weng, D.L. Shen and C.X. Tan, Chin. J. Org. Chem., 27, 126 (2007).
- S. Ozaki, Chem. Rev., 72, 457 (1972).
- J.Q. Weng, H.J. Liu, X.H. Liu, C.X. Tan and D.L. Shen, Chin. J. Pesticide Sci., 12, 463 (2010).
- P. Yang, C.X. Tan, D.L. Shen, Q. Fu and X.L. Kong, J. Zhejiang Univ. Technol., 35, 19 (2007).
- F.L. Yang, Z.J. Liu, X.B. Huang and M.W. Ding, J. Heterocycl. Chem., 41, 77 (2004).
References
X.H. Liu, Y.X. Shi, Y. Ma, C.Y. Zhang, W.L. Dong, P. Li, B.L. Wang, B.J. Li and Z.M. Li, Eur. J. Med. Chem., 44, 2782 (2009).
Y. Sawada, T. Yanai and H. Nakagawa, Pest Manage. Sci., 59, 49 (2003).
J.Q. Weng, D.L. Shen, C.X. Tan and X.M. Ou, Chin. J. Org. Chem., 26, 1106 (2006).
W.L. Dong, Z.X. Liu, X.H. Liu, Z.M. Li and W.G. Zhao, Eur. J. Med. Chem., 45, 1919 (2010).
Z.Z. Zhou, Q. Chen and G.F. Yang, Chin. J. Org. Chem., 28, 1385 (2008).
N. Muhammad, N. Muhammad, B. Iftikhar and R. Salma, J. Chem. Soc. Pak., 30, 780 (2008).
W. Wang, G.P. Zhang, B.A. Song, H. Wang, L.H. Jin, D.Y. Hu and S. Yang, Chin. J. Org. Chem., 27, 279 (2007).
Q.M. Wang, H. Li, Y.H. Li and R.Q. Huang, J. Agric. Food Chem., 52, 1918 (2004).
P.C. David, V.E. Roy and T.H. Roy, J. Agric. Food Chem., 29, 640 (1981).
R.E. Menzer and J.E. Casida, J. Agric. Food Chem., 13, 102 (1965).
X.H. Liu, C.X. Tan and J.Q. Weng, Phosphorus Sulfur Silicon Rel. Elem., 186, 552 (2011).
S. Vishnoi, V. Agrawal and V.K. Kasana, J. Agric. Food Chem., 57, 3261 (2009).
J.Q. Weng, D.L. Shen and C.X. Tan, Chin. J. Org. Chem., 27, 126 (2007).
S. Ozaki, Chem. Rev., 72, 457 (1972).
J.Q. Weng, H.J. Liu, X.H. Liu, C.X. Tan and D.L. Shen, Chin. J. Pesticide Sci., 12, 463 (2010).
P. Yang, C.X. Tan, D.L. Shen, Q. Fu and X.L. Kong, J. Zhejiang Univ. Technol., 35, 19 (2007).
F.L. Yang, Z.J. Liu, X.B. Huang and M.W. Ding, J. Heterocycl. Chem., 41, 77 (2004).