首页> 外文期刊>Der chemica Sinica >Design, Synthesis and Biological Activity of Some Benzimidazoles Derivatives 3-Chloro-4-(Substituted--phenyl-1-(4-{1-[2'-(2H-tetrazol-5-yl)-biphenyl-4- ylmethyl]-1H-benzimidazol-2yl}-phenyl)-azetidin-2-ones
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Design, Synthesis and Biological Activity of Some Benzimidazoles Derivatives 3-Chloro-4-(Substituted--phenyl-1-(4-{1-[2'-(2H-tetrazol-5-yl)-biphenyl-4- ylmethyl]-1H-benzimidazol-2yl}-phenyl)-azetidin-2-ones

机译:某些苯并咪唑衍生物3-氯-4-(取代的-苯基-1-(4- {1- [2'-(2H-四唑-5-基)-联苯-4-基甲基]的设计,合成和生物活性-1H-苯并咪唑-2基}-苯基)-氮杂环丁烷-2-酮

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A novel method for the synthesis of novel 3-Chloro-4(4-chloro-phenyl-1-(4-{1-[2'-(2H-tetrazol- 5-yl)-biphenyl-4-ylmethyl]-1H-benzimidazol-2yl}-phenyl)-azetidin-2-one derivatives have been reported. Structures of all the synthesized compounds have been corroborated on the basis of elemental IR, 1H NMR, 13C NMR and Mass spectro-analytical data. Many Schiff bases were prepared by condensation reaction of nitro compound containing biphenyl tetrazole with aromatic aryl aldehydes derivatives with azetidin-2-one. The synthesized compounds were screened for AT1 Angiotension (A II) Receptor Antagonist activity. The nitro, chlorine, hydroxy, florine, iodo compound containing biphenyl tetrazole Schiff bases azetidin-2-one shows good activity compared with losartan and Telmisartan.
机译:合成新颖的3-Chloro-4(4-chloro-phenyl-1-(4- {1- [2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl] -1H)的新方法-苯并咪唑-2-基}-苯基)-氮杂环丁烷-2-one衍生物的报道,根据元素IR,1 H NMR,13 C NMR和质谱分析数据,证实了所有合成化合物的结构。含联苯四唑的硝基化合物与芳基醛衍生物与氮杂环丁烷-2-一的缩合反应制得的化合物经筛选具有AT1血管紧张素(A II)受体拮抗活性,其中硝基,氯,羟基,植物精,碘化合物与氯沙坦和替米沙坦相比,含有联苯四唑席夫碱的氮杂环丁烷-2-酮显示出良好的活性。

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