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Abstract
A novel heterocyclic library were synthesized, characterized and tested for biological evaluation against bacteria and fungus. This novel series of substitute N-(4-(3-oxomorpholino)phenyl)-2-(4-((phenylamino)-methyl)-1H-1,2,3-triazol-1-yl)acetamide via click chemistry approach in the presence of DMF:H2O:n-BuOH and CuSO4·5H2O in good yield. The title compounds have been synthesized with several structural variations. The synthesized compounds were screened for antimicrobial activity against standard drugs. The structure of synthesized compounds characterized by their spectral (IR, 1H NMR and mass) data. The purity of the synthesized compounds was confirmed by TLC.
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References
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References
C.H. Zhou and Y. Wang, Recent Researches in Triazole Compounds as Medicinal Drugs, Curr. Med. Chem., 19, 239 (2012); https://doi.org/10.2174/092986712803414213
S.K. Monfared, Ph.D. Thesis, 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, France (2014).
H.C. Kolb, M.G. Finn and K.B. Sharpless, Click Chemistry: Diverse Chemical Function from a Few Good Reactions, Angew. Chem. Int. Ed., 40, 2004 (2001); https://doi.org/10.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5
H. Adolfsson, A. Converso and K.B. Sharpless, Comparison of Amine Additives Most Effective in the New Methyltrioxorhenium-Catalyzed Epoxidation Process, Tetrahedron Lett., 40, 3991 (1999); https://doi.org/10.1016/S0040-4039(99)00661-9
H.C. Kolb and K.B. Sharpless, The Growing Impact of Click Chemistry on Drug Discovery, Drug Discov. Today, 8, 1128 (2003); https://doi.org/10.1016/S1359-6446(03)02933-7
H. Li, R. Aneja and I. Chaiken, Click Chemistry in Peptide-Based Drug Design, Molecules, 18, 9797 (2013); https://doi.org/10.3390/molecules18089797
R. Hoogenboom, Thiol-Yne Chemistry: A Powerful Tool for Creating Highly Functional Materials, Angew. Chem. Int. Ed., 49, 3415 (2010); https://doi.org/10.1002/anie.201000401
R. Tong, L. Tang, L. Ma, C. Tu, R. Baumgartner and J. Cheng, Smart Chemistry in Polymeric Nanomedicine, Chem. Soc. Rev., 43, 6982 (2014); https://doi.org/10.1039/C4CS00133H
X. Zhang and Y. Zhang, Applications of Azide-Based Bioorthogonal Click Chemistry in Glycobiology, Molecules, 18, 7145 (2013); https://doi.org/10.3390/molecules18067145
S.B. Rose and R.E. Miller, Studies with the Agar Cup-Plate Method: I. A Standardized Agar Cup-Plate Technique, J. Bacteriol., 38, 525 (1939); https://doi.org/10.1128/jb.38.5.525-537.1939