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首页> 外文期刊>International Research Journal of Pure and Applied Chemistry >Green Tamarind Extract Catalyzed Synthesis of 4-Amino-1,2,4-Triazole Derivatives and Their In-vitro Antimicrobial Activity
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Green Tamarind Extract Catalyzed Synthesis of 4-Amino-1,2,4-Triazole Derivatives and Their In-vitro Antimicrobial Activity

机译:绿色罗望子提取物催化合成4-氨基-1,2,4-三唑衍生物及其体外抗微生物活性

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In several organic synthesis and chemical transformations, the use of green chemistry has decreased the reaction time and chemical waste. Due to the tremendous advantages of green chemistry, the paper presents the synthesis of benzylidene derivatives of 4-amino-1,2,4-triazole by reacting it with various substituted aldehydes/benzaldehydes using different catalytic amount(ln mL) of tamarind extract/glacial acetic acid as a catalyst by conventional and microwave method.? All the synthesized compounds (1-7) were characterized using spectroscopic techniques viz. UV, IR, and 1H NMR. Antimicrobial activity of all the compounds was done using negative gram bacteria i.e. Pseudomonas aeruginosa, Klebsiella sp., and Enterobacter sp. against standard Ampicillin. Compound 2 containing 4-nitro substitution increased the antimicrobial activity as compared to other Enterobacter sp, but none of them showed better In-vitro antimicrobial potential than standard ampicillin. All the synthesized Schiff bases differed significantly from one another within the range of test concentrations.
机译:在几种有机合成和化学转化中,使用绿色化学的使用降低了反应时间和化学废物。由于绿色化学的巨大优点,本文通过使用不同催化量(LN ML)的罗望子提取物(LN ML)与各种取代的醛/苯甲醛反应来合成4-氨基-1,2,4-三唑的合成/通过常规和微波法作为催化剂的冰醋酸作为催化剂。所有合成化合物(1-7)都是使用光谱技术viz的表征。 UV,IR和1H NMR。所有化合物的抗微生物活性使用负革兰氏菌,即Pseudomonas铜绿假单胞菌,Klebsiella sp。和肠杆菌。针对标准氨苄青霉素。与其他肠杆菌SP相比,含有4-硝基取代的化合物2增加了抗微生物活性,但它们均未显示出比标准氨苄青霉素更好的体外抗微生物潜力。所有合成的Schiff碱基在测试浓度范围内彼此有显着不同。

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