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Synthesis, Characterization and Bioactivity Research of a Derivative of Secnidazole: 1-(2-Chloropropyl)-2-methyl-5-nitro-1H-imidazole

机译:塞克硝唑衍生物1-(2-氯丙基)-2-甲基-5-硝基-1H-咪唑的合成,表征及生物活性研究

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Abstract A secnidazole derivative, 1-(2-chloropropyl)-2-methyl-5-nitro-1H-imidazole (1), was synthesized and its single crystals were successfully grown in the mixture of ethanol/chloroform (3:1) by slow evaporation at room temperature. Its structure was confirmed by 1H NMR, 13C NMR, mass spectra, elemental analyses and X-ray single crystal diffraction. Crystal structure analysis revealed that 1 crystallized in the triclinic, space group P [`1] overline{1} with the following unit cell parameters: a = 6.5339(7) Ǻ, b = 7.5487(8) Ǻ, c = 9.7238(10) Ǻ, α = 92.894°(2), β = 96.165(2)°, γ = 102.710°(2), V = 463.78(8) Å3, Z = 2. Furthermore, this compound exhibited better anti-urease activity than secnidazole and acetyl-hydroxy acid when evaluated for antimicrobial activity against Helicobacter pylori.
机译:摘要合成了塞尼达唑衍生物1-(2-氯丙基)-2-甲基-5-硝基-1H-咪唑(1),并在乙醇/氯仿(3:1)混合物中成功地单晶生长。在室温下缓慢蒸发。通过 1 核磁共振, 13 核磁共振,质谱,元素分析和X射线单晶衍射确定其结构。晶体结构分析表明,在三斜空间群P [`1]上线{1}中结晶的1具有以下晶胞参数:a = 6.5339(7),b = 7.5487(8),c = 9.7238(10) )Ǻ,α= 92.894°(2),β= 96.165(2)°,γ= 102.710°(2),V = 463.78(8)Å 3 ,Z = 2。当评估该化合物对幽门螺杆菌的抗菌活性时,该化合物具有比塞尼达唑和乙酰羟基酸更好的抗脲酶活性。

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