Synthesis, Characterization and Biological Evaluation of Novel Substitute 2,2'-(4,4'-((Phenylazanediyl)Bis(Methylene)) Bis (1h-1,2,3-Triazole-4,1-Diyl))Bis(N-(4-(3-Oxomorpholino) Phenyl)Acetamide) Via Click Chemistry Approach
Keywords:
Acetamide, Click, Chemistry, Biological, Activities, FungalAbstract
In current work we synthesized novel series of triazole derivatives of 2,2'-(4,4'- ((phenylazanediyl)bis(methylene)) bis (1H-1,2,3-triazole-4,1-diyl)) bis (N-(4-(3-oxomorpholino)phenyl)acetamide) via click chemistry approach in the presence DMF:H2O:n-BuOH, and CuSO4.5H2O of in good yield. The different studies indicate that newly synthesized novel compounds possess moderate to good biological activities. The title compounds have been synthesized with several structural variations biological evaluation of entirely synthesized compounds have been carried out in vitro for their antibacterial and antifungal efficacy against various bacterial and fungal strains. The structure of synthesized compounds characterized by their spectral (IR, 1H NMR and Mass) data. All compounds purity confirmed by TLC.
References
- C. H. Zhou, Y. Wang, Curr. Med. Chem. 2012, 19, 239–280.
- S. K. Monfared, Synthesis and Cytotoxicity Evaluation of Small 1, 4-Triazolic Derivatives against B16 Melanoma Cell Lines and a Methodolgy Study on the Synthesis of Propargyl Ethers from Their Corresponding Propargyl Esters without Catalyst and under Microwave Irradiatio, Université Pierre et Marie Curie-Paris VI, 2014.
- H. C. Kolb, M. G. Finn, K. B. Sharpless, Angew. Chemie - Int. Ed. 2001, 40, 2004– 2021.
- H. Adolfsson, A. Converso, K. B. Sharpless, Tetrahedron Lett. 1999, 40, 3991– 3994.
- H. C. Kolb, K. B. Sharpless, Drug Discov. Today 2003, 8, 1128–1137.
- H. Li, R. Aneja, I. Chaiken, Molecules 2013, 18, 9797–9817.
- R. Hoogenboom, Angew. Chemie Int. Ed. 2010, 49, 3415–3417.
- R. Tong, L. Tang, L. Ma, C. Tu, R. Baumgartner, J. Cheng, Chem. Soc. Rev. 2014,43, 6982–7012.
- X. Zhang, Y. Zhang, Molecules 2013, 18, 7145–7159.
- C.-F. Chan, K.-S. Huang, M.-Y. Lee, C.-H. Yang, C.-Y. Wang, Y.-S. Lin, Curr. Org. Chem. 2014, 18, 204–215.
- D. Sun, M. Babar Shahzad, M. Li, G. Wang, D. Xu, Mater. Technol. 2015, 30, B90– B95.
- A. Brochot, A. Guilbot, L. Haddioui, C. Roques, Microbiologyopen 2017, 6, e00459.
- I. Al-Adham, R. Haddadin, P. Collier, Russell, Hugo Ayliffe’s Princ. Pract. Disinfect. Preserv. Steriliz. 2013, 5–70. \
- S. B. Rose, R. E. Miller, J. Bacteriol. 1939, 38, 525.
Downloads
Published
Issue
Section
License
Copyright (c) IJSRST

This work is licensed under a Creative Commons Attribution 4.0 International License.