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盐酸西替利嗪的NMR研究

NMR studies on cetirizine hydrochloride

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【作者】 李茜沈文斌邹巧根

【Author】 LI Qian, SHEN Wen bin *, ZOU Qiao gen (Center for Instrumental Analysis, China Pharmaceutical University, Nanjing 210009, China)

【机构】 中国药科大学分析测试中心中国药科大学分析测试中心 江苏南京210009江苏南京210009江苏南京210009

【摘要】 目的 研究盐酸西替利嗪在DMSO d6溶剂中的核磁共振现象并对其质子和碳信号进行归属。方法 测定其在不同温度和加入重水条件下的各种 1D和 2D核磁共振谱。结果 室温下以DMSO d6为溶剂时 ,哌嗪环及与其N原子相连的碳、氢信号均呈现多个峰或宽峰 ,提高温度或加入重水后 ,其碳、氢信号均出现“合并”或变窄现象。结论 室温下在DMSO d6溶剂中 ,与核磁共振“时间尺度”相比 ,不同构象的盐酸西替利嗪并存 ;随着温度的提高 ,不同构象能快速互变 ,而加入重水则形成稳定构象

【Abstract】 Aim To study the NMR phenomena of cetirizine hydrochloride and assign all proton and carbon signals in NMR spectra. Methods To record the 1D and 2D NMR spectra of cetirizine hydrochloride while changing the experimental temperature and adding D 2O into the solution. Results More than one NMR signal or broad peak resulting from piperazine and the attached groups with N atom were given in DMSO d 6 solution at room temperature. “Coalescence” or narrowing had occurred for the proton and carbon signals when the experimental temperature was increased or D 2O was added into the solution. Conclusion Compared with the NMR “time scale”, there are more than one conformation of cetirizine hydrochloride in DMSO d 6 solution at room temperature. The different conformation will be exchanged fast while temperature rised and the stable conformation will be existed while D 2O was added into the solution.

  • 【文献出处】 药学学报 ,Acta Pharmaceutica Sinica , 编辑部邮箱 ,2003年10期
  • 【分类号】R917
  • 【被引频次】4
  • 【下载频次】154
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