The Antifungal Effect of some 4-Chloro-6-Methoxy-N, N-Dimethylpyrimidin-2-Amine Derivatives Containing a Heterocyclic Compound on the Important types of Fungi
Nadhir N.A. Jafar1, Ibtihial M Abdul Mahdi2, Mahmoud Hussein Hadwan1★, Ameer A, Alameri1★ Corresponding author
- 1Department of Chemistry, College of Science, University of Babylon, IRAQ.
- 2Department of Biology, College of Science, University of Babylon, IRAQ.
CORRESPONDENCE
Mahmoud Hussein Hadwan
Department of Chemistry, College of Science, University of Babylon, IRAQ.
Received: 03-04-2017; Revised: 23-05-2017; Accepted: 15-07-2017.
Volume 9, Issue 4 · pp. 463–467 · PUBLISHED · DOI: 10.5530/jyp.2017.9.91
ABSTRACT
Objective: 4-methoxy-N, N-dimethyl-6-(phenylthio) pyrimidin-2-amine, 4-(benzo[d]thiazol-2-ylthio)-6-methoxy-N,N-dimethylpyrimidin-2-amine, 4-(4-(1,2,3-selenadiazol-4-yl)phenoxy)-6-methoxy-N,N 2-amine and 4-(4-(1,2,3-thiadiazol-4-yl)phenoxy)-6-methoxy-N,N 2-amine have been synthesized. Method: The prepared compounds were synthesized by nucleophilic displacement of chloride substituted in pyrimidine heterocyclic ring. Results: The synthesized compounds were being identified by different methods included TLC technique, IR, 1H-NMR and 13C-NMR spectrophotometers. All compounds confirmed by elemental analysis. The biological activity of these new compounds investigated against some fungi like Aspergillus terreus and Aspergillus niger, the results was Aspergillus terreus more effected by antifungal compare with Aspergillus niger, the effect ration 0.98, 1.32 with 200μM respectively and the compound number (2) has more effect than other compounds. Conclusion: It is concluded that synthesized dimethylpyrimidin-derivatives are biologically active and developed into useful Antifungal agents.
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Jafar, N. N., Mahdi, I. M. A., Hadwan, M. H., & Alameri, A. A. (). The Antifungal Effect of some 4-Chloro-6-Methoxy-N, N-Dimethylpyrimidin-2-Amine Derivatives Containing a Heterocyclic Compound on the Important types of Fungi. Journal of Young Pharmacists, 9(4), 463–467. https://doi.org/10.5530/jyp.2017.9.91
