首页> 外文期刊>American Journal of Organic Chemistry >p-TSA Catalysted, One-Pot Synthesis and Antimicrobial Evaluation of Some Novel Fused Dipyrazolo-1,4-Dihydropyridine Derivatives
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p-TSA Catalysted, One-Pot Synthesis and Antimicrobial Evaluation of Some Novel Fused Dipyrazolo-1,4-Dihydropyridine Derivatives

机译:p -TSA催化,一锅合成和一些新型熔融二吡唑并-1,4-二氢吡啶衍生物的抗菌性能

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Some novel dipyrazolo-1,4-dihydropyridine derivatives have been synthesized via one-pot, multi-component condensation of N-phenylpyrazole, aldehyde and ammonium acetate using p-TSA as catalyst. The fused dipyrazolo-1,4-dihydropyridine molecules without using expensive starting materials and the molecules are obtained in excellent yield without using any special purification technique. The synthesized compounds were screened for their in vitro antibacterial and antifungal activity against six bacterial and four fungal species. Among these 4a, 4e and 4h exhibited significant antibacterial activity against various bacterial and fungal strains.
机译:通过 p -TSA作为底物,通过N-苯基吡唑,醛和乙酸铵的一锅多组分缩合合成了一些新颖的双吡唑-1,4-二氢吡啶衍生物。催化剂。不使用昂贵的起始原料而稠合的双吡唑并-1,4-二氢吡啶分子,并且无需使用任何特殊的纯化技术就可以以优异的收率获得分子。筛选了合成的化合物对六种细菌和四种真菌的体外抗菌和抗真菌活性。在这些 4a , 4e 和 4h 中,它们对各种细菌和真菌菌株均表现出显着的抗菌活性。

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