The titled compounds(5) were synthesized by the hydrazone reaction of aromatic aldehydes and 3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-hydrazinyl-1,2,4,5-tetrazine(4) prepared from hydrazine hydrate and guanidine nitrate via cyclization,oxidation and hydrazine reaction.They had been identified by elemental analysis,1H NMR,IR and MS.The results of preliminary bioassays showed that parts of as-synthesized compounds(5) exhibit moderate inhibitory activity to E.coli.,S.aureus and B.subtilis.%以水合肼和硝酸胍为原料,经过环合、氧化和肼化,得到3-(3,5-二甲基-1H-吡唑-1-基)-6-肼基-1,2,4,5-四嗪(4),以此为原料和不同芳香醛发生腙化反应,得到系列1-芳基亚甲基-2-(6-(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪-3-基)肼(5),产物经元素分析、1H NMR、IR和MS表征。所合成的系列化合物抗菌活性测试表明,它们对大肠杆菌、金黄色葡萄球菌、枯草杆菌等3种细菌表现出一定程度的抑制活性。
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