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Synthesis of New 1,2,4-Triazole[3,4-b][1,3,4]thiadiazoles Bearing Pyrazole as Potent Antimicrobial Agents

机译:以吡唑为有效抗菌剂的新型1,2,4-三唑[3,4-b] [1,3,4]噻二唑的合成

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A new series of 6-(aryl/heteryl)-3-(5-methyl-1-phenyl-1 H -4-pyrazolyl)[1,2,4]triazolo[3,4- b ][1,3,4]thiadiazoles ( 7a — j ) has been synthesized by the reaction of 4-amino-5-(5-methyl-1-phenyl-1 H -4-pyrazolyl)-4 H -1,2,4-triazol-3-yl-hydrosulfide ( 6 ) with POCl3 and the corresponding aryl/heteryl carboxylic acid, in ethanol at reflux temperature for 12 h. All the synthesized compounds were tested for in vitro activities against certain strains of bacteria such as Staphylococcus aureus , Bacillus subtilis , Escherichia coli and fungi such as Aspergillus niger , Aspergillus nodulans , Alternaria alternate . Compounds having 4-chlorophenyl ( 7d ), 4-aminophenyl ( 7f ), 4-nitrophenyl ( 7h ) and 3-pyridyl ( 7i ) substituents at 6-position of thiadiazole ring, showed marked inhibition of bacterial and fungal growth nearly equal to the standards. The other new compounds also showed appreciable activity against the test bacteria and fungi.
机译:一个新的6-(芳基/杂基)-3-(5-甲基-1-苯基-1 H -4-吡唑基)[1,2,4]三唑[3,4-b] [1,3, 4]噻二唑(7a_j)通过4-氨基-5-(5-甲基-1-苯基-1 H -4-吡唑基)-4 H -1,2,4-三唑-3的反应合成在乙醇中,在回流温度下,用POCl 3 和相应的芳基/杂芳基羧酸制备正丁基氢硫化物(6)。测试了所有合成化合物对某些细菌菌株(如金黄色葡萄球菌,枯草芽孢杆菌,大肠杆菌和真菌,如黑曲霉,诺氏曲霉,交替杆菌)的体外活性。在噻二唑环的6位上具有4-氯苯基(7d),4-氨基苯基(7f),4-硝基苯基(7h)和3-吡啶基(7i)取代基的化合物对细菌和真菌的生长具有明显的抑制作用,几乎等于标准。其他新化合物也对测试细菌和真菌表现出明显的活性。

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