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Diverse synthetic approach for sulfur and nitrogen-containing spiroheterocycles from dimedone and their pharmacological evaluation

机译:来自Dimedone的含硫和含氮螺旋形循环系的多种合成方法及其药理学评估

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摘要

Novel spiro(3-hydroxy-5,5-dimethyl)-1,5'-(2'-substituated[1,3,4]-oxadiazole/thiadiazolo[3,2-c] thiazolines and 3-hydroxy-5,5-dimethyl-spiro[cyclohex-2-ene-thiazolo/thiazino[3,2-b]-s-tetrazine were prepared from previously reported hydrazone, semicarbazone, carbazone, and spiro-s-tetrazine intermediates derived from dimedone precursor. All the newly synthesized heterocycles have been characterized by analytical and spectral (H-1 NMR and C-h NMR) data and screened their in vitro antibacterial activity against gram negative bacteria Escherichia coli and gram positive bacteria Staphylococcus aureus. Some of the compounds showed moderate to good activities towards the bacteria chosen.
机译:新型螺螺(3-羟基-5,5-二甲基)-1,5' - (2' - 替代[1,3,4] - 脱唑/噻唑啉和3-羟基 - 5, 从先前报道的腙,氨基脲,咔唑酮和螺旋-S-四嗪中间体制备5-二甲基 - 螺唑(环己-2-Ene-Thiazolo / Thiazino [3,2-B] -s-四唑嗪[3,2-B] -S-四唑类衍生自Dimedone前体。所有 新合成的杂环的特征在于分析和光谱(H-1 NMR和CH NMR)数据,并筛选其对革兰阴性细菌大肠杆菌和克革氏阳性细菌金黄色葡萄球菌的体外抗菌活性。一些化合物显示出中度至良好的活性 朝向所选细菌。

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