首页> 外国专利> COMPLEXONES WITH THE STRUCTURE OF N-2-(AZOL-1(2)-YL)ETHYLIMINODIACETIC ACIDS, SYNTHESIS, ANALYTICAL STUDY AND BIOLOGICAL APPLICATIONS

COMPLEXONES WITH THE STRUCTURE OF N-2-(AZOL-1(2)-YL)ETHYLIMINODIACETIC ACIDS, SYNTHESIS, ANALYTICAL STUDY AND BIOLOGICAL APPLICATIONS

机译:具有N-2-(AZOL-1(2)-YL)乙基亚氨基二乙酸结构的配合物,合成,分析研究及生物学应用

摘要

Complexones having the structure of N-2-(azol-1(2)-yl(ethyl-iminodiacetic acids, synthesis, analytical study and biological applications, characterized by their complexing capacity over Ca2+, Mg2+ ions and other bivalent cations, lanthanides and transition metals. In the formula azolN-CH2-CH2-N(CH2-CO2R)2 (I), azol is pirazol; 3,5-dimethylpirazol; indazol; etc. and R is alkyl or H or Na. The compounds having the general formula (I), are obtained by an alkylation reaction of methyl iminodiacetate with N-bromoethylazols and further hydrolysis in acid or basic medium. The process may be modified by alternative synthetic processes which involve N-aminoethylazols as starting materials or the use of cyclization processes in the preparation of N-substituted azol. They can be applied in spectroscopy and nuclear magnetic resonance (NMR) imaging of hydrogen or other nuclei as extrinsic probes of Ca2+, Mg2+ or other metal ions and as contrast agents, in solutions, biological extracts, tissues, entire animals and human beings.
机译:具有N-2-(azol-1(2)-yl(ethyl-iminodiacetic acid)结构的配合物,其合成,分析研究和生物学应用的特征是其在Ca 2上的络合能力。 + ,Mg 2 + 离子和其他二价阳离子,镧系元素和过渡金属在式中azolN-CH 2 -CH 2 -N(CH 2 -CO 2 R) 2 (I),氮杂为吡唑; 3,5-二甲基吡唑;吲唑;等通式(I)的化合物是通过亚氨基二乙酸甲酯与N-溴乙基偶氮烷基的烷基化反应并在酸或碱性介质中进一步水解而制得的,该方法可通过替代合成法进行修饰。 N-氨基乙基偶氮为起始原料的方法或在N-取代的氮杂化合物的制备中使用环化方法的方法,它们可用于氢或其他核的光谱学和核磁共振成像,作为Ca 2 + ,溶液,生物提取物,组织,整个动物和人类中的Mg 2 + 或其他金属离子以及作为造影剂。

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