Articles

One Pot Synthesis of 3-Substituted-1-morpholino-1,2,4-triazole Mannich Bases and Their Activity Evaluation

  • Zhang Chenglu ,
  • Tang Jie ,
  • Yin Liying ,
  • Xi Huan ,
  • Guo Yang ,
  • Sun Lijie
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  • College of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029

Received date: 2015-07-24

  Revised date: 2015-10-08

  Online published: 2015-10-23

Supported by

Project supported by the Science and Technology Research Program of Liaoning Provincial Department of Education (No. 2009A426).

Abstract

15 Schiff bases were synthesized by the reactions of 3-p-chlorophenyl, 3-p-methoxyphenyl and 3-n-pentyl-1,2,4-triazole with five different aromatic aldehydes, respectively. Then 14 novel Mannich bases (PCTABM, PMTABM and PETABM) were first afforded by the reactions of Schiff bases with formaldehyde and morpholine through multi-component one-pot reaction. In order to explore the effect of different 3-substituted groups on biological activities, four Mannich bases FcTABM of 3-ferrocenyl-1,2,4-triazole were also synthesized starting from 3-ferrocenyl-1,2,4-triazole by the similar method. IR, 1H NMR and HRMS were used to characterize the structure of the target molecules. The biological activities of the target molecules were evaluated. As a result, the target compounds exhibited excellent activities in plant growth regulators and herbicidal activity. There are 14 target compounds exhibited excellent inhibitory activity against Cdc25B, in which the IC50 values of 7c, 8e, 9e, 10b10e IC50 were all smaller than the reference Na3VO4, which were expected to be Cdc25B inhibitors.

Cite this article

Zhang Chenglu , Tang Jie , Yin Liying , Xi Huan , Guo Yang , Sun Lijie . One Pot Synthesis of 3-Substituted-1-morpholino-1,2,4-triazole Mannich Bases and Their Activity Evaluation[J]. Chinese Journal of Organic Chemistry, 2016 , 36(2) : 358 -362 . DOI: 10.6023/cjoc201507029

References

[1] Ashok, M.; Holla, B. S.; Poojary, B. Eur. J. Med. Chem. 2007, 42, 1095.
[2] Roman, G. Eur. J. Med. Chem. 2015, 89, 743.
[3] Li, G. H.; Yang, H. Chin. J. Org. Chem. 2008, 28, 1918 (in Chinese). (李国华, 杨红, 有机化学, 2008, 28, 1918.)
[4] Navidpour, L.; Shafaroodi, H.; Abdi, K.; Amini, M.; Ghahremani, H. M.; Dehpour, A. R.; Shafiee, A. Bioorg. Med. Chem. 2006, 14, 2507.
[5] Holla, B. S.; Veerendra, B.; Shivananda, M. K.; Poojary, B. Eur. J. Med. Chem. 2003, 38, 759.
[6] Wang, B. L.; Shi, Y. X.; Ma, Y.; Liu, X. H.; Li, Y. H.; Song, H. B.; Li, B. J.; Li, Z. M. J Agric Food Chem. 2010, 58, 5515.
[7] Deng, X. M.; Wang, J. H.; Zhang, J. M.; Sim, T.; Kim, N. D.; Sasaki, T.; Luther, W.; George, R. E.; Janne, P. A.; Gray, N. S. Med. Chem. Lett. 2011, 2, 379.
[8] Kunj, B. M.; Vinod, K. T. J. Org. Chem. 2014, 79, 5752.
[9] Burbuliene, M. M.; Jakubkiene, V.; Mekuskiene, G.; Udrenaitea, E.; Smiciusa, R.; Vainilaviciusa, P. Farmaco 2004, 59, 767.
[10] Koparir, M.; Orek, C.; Parlak, A. E.; Söylemez, A.; Koparir, P.; Karatepe, M.; Dastan, S. D. Eur. J. Med. Chem. 2013, 63, 340.
[11] Jakubkiene, V.; Burbuliene, M. M.; Mekuskiene, G.; Emilija, U.; Gaidelis, P.; Vainilavi?ius, P. Farmaco 2003, 58, 323.
[12] Ashok, M.; Holla, B. S.; Poojary, B. Eur. J. Med. Chem. 2007, 42, 1095.
[13] Holla, B. S.; Rao, B. S.; Shridhara, K.; Akberali, P. M. Farmaco 2000, 55, 338.
[14] Hu, G. Q.; Wang, G. Q.; Duan, N. N.; Wen, X. Y.; Cao, T.Y.; Xie, S. Q.; Huang, W. L. Acta Pharm. Sin. B 2012, 2, 312.
[15] Kaminski, K.; Obniska, J.; Chlebek, I.; Wiklik, B.; Rzepka, S. Bioorg. Med. Chem. 2013, 21, 6821.
[16] Arafa, W. A. A; Mohamed, A. S. Chin. J. Chem. 2011, 29, 1661.
[17] Mohamed, R. A. Molecules 2014, 19, 18897.
[18] Mostafa, A. H.; Refaat, M. S.; Mohammed, A. A.; Mohammed, F. M. Arch. Pharm. Res. 2011, 34, 1239.
[19] Tsuchiya, A.; Hirai, G.; Koyama, Y.; Oonuma, K.; Otani, Y.; Osada, H.; Sodeoka, M. Med. Chem. Lett. 2012, 3, 294.
[20] Li, Q. H.; Wang, M. M. Chem. Res. Appl. 2010, 22, 186 (in Chinese). (李清寒, 王苗苗, 化学研究与应用, 2010, 22, 186.)
[21] Zhu, C. A.; Wu, F. Y.; Wang, X.; Gao, L. N.; Weng, Q. F.; Shi, L.; Zhang, C. L. Chin. J. Appl. Chem. 2014, 31, 455 (in Chinese). (朱长安, 武飞宇, 王雪, 高丽娜, 翁前锋, 石丽, 张成路, 应用化学, 2014, 31, 455.)
[22] Lavecchia, A.; Giovanni, C. D.; Pesapane, A.; Montuori, N.; Ragno, P.; Martucci, N. M.; Masullo, M.; Vendittis, E. D. J. Med. Chem. 2012, 55, 4142.
[23] Sahoo, P. K.; Sharma, R.; Pattanayak, P. Med. Chem. Res. 2010, 19, 127.
[24] George, T.; Mehta, D. V.; Tahilramani, R.; David, J.; Talwalker, P. K. J. Med. Chem. 1971, 14, 335.
[25] Zhang, C. L.; Wang, X.; Guo, Y. Wu, Y. F.; Gao, L. N.; Sun, L. J.; Chai, J. H.; Zhu, C. A. Chin. J. Org. Chem. 2014, 34, 2331 (in Chinese). (张成路, 王雪, 国阳, 吴一非, 高丽娜, 孙丽杰, 柴金华, 朱长安, 有机化学, 2014, 34, 2331.)
[26] Gupta, A, K.; Prachand, S.; Patel, A.; Jain, S. Int. J. Pharm. Life Sci. 2012, 3, 1848.

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