Synthesis, Characterization and bioactivity Study of some new Trizole malimide Compounds

None Muhand K. Taher AL- Tememi, None Faeza A. AL-Mashal
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Abstract

New two compounds of a five-membered heterocyclic rings triazoles compounds (T1) 4-(4,6-dioxo-5-(p-tolyl)-4,5,6,6atetrahydropyrrolo[3,4-d][1,2,3] triazol-1(3aH)-yl)benzene sulfonamide & (T2) 4-(5-(4-chlorophenyl)-4,6-dioxo-4,5,6,6atetrahydropyrrolo[3,4-d][1,2,3]triazol-1(3aH)-yl) which were synthesized by 1,3 di polar cycloaddition reaction of 4-azidobenzenesulfonamide with (A1) (1-(p-tolyl)-1H-pyrrole-2,5-dione) & (A2) (1-(4-chlorophenyl)-1Hpyrrole-2,5-dione) followed by thermal process. T1 & T2 compounds were synthesized at 56 °C in the present of acetone as a solvent. The products were recrystallized from acetone and ether (1:2), dried and characterized using Fourier transform infrared FT-IR, 1HNMR, and mass spectra. The antibacterial activities of triazoles (T1 & T2) were studied. Antibacterial and anti-fungi activity, Hole-in-plate and disk bioassay procedure methods were used to determine activity of prepared compounds (T1 & T2) against (Aspergillus Terreus,fungus & Psedomounus Aeroginosa, Kocuria Kristinie , Enterobactar Cloacae. , Aeromonase veronii and Staphylococcus Lentus) bacteria.
一些新型三唑酰亚胺化合物的合成、表征及生物活性研究
新的两种五元杂环三唑类化合物(T1) 4-(4,6-二氧基-5-(对苯基)-4,5,6,6四氢吡咯[3,4-d][1,2,3]三唑-1(3aH)-基)苯磺酰胺(T2) 4-(5-(4-氯苯基)-4,6-二氧基-4,5,6,6四氢吡咯[3,4-d][1,2,3]三唑-1(3aH)-基)与(A1)(1-(对甲苯基)- 1h -吡咯-2,5-二酮)和amp的1,3双极性环加成反应合成的4-(5-(4-氯苯基)-4,6-二氧基-4,6-四氢吡咯-4,5,6,6)(A2)(1-(4-氯苯基)- 1hpyrrole -2,5-二酮),然后进行热反应。T1和T2化合物在56℃下以丙酮为溶剂合成。产物由丙酮和醚(1:2)重结晶,干燥,并用傅里叶变换红外FT-IR, 1HNMR和质谱进行表征。三唑类(T1 &T2)进行研究。抑菌和抗真菌活性,采用板孔法和圆盘法测定制备的化合物(T1 &T2)抗土曲霉,真菌;铜绿假单胞菌,Kocuria kristine,肠杆菌阴道炎。维罗氏气单胞酶和香菇葡萄球菌)细菌。
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