高比活度碳-14标记毒氟磷的合成与分析

    Synthesis and analysis of carbon-14 labelled Dufulin with high specific activity

    • 摘要: 以14C碳酸钡为放射性同位素原料,通过格氏反应、Curtius重排、亲核加成、硫代及关环等7步反应,制备了同位素碳-14标记的毒氟磷粗品,经反相高效液相色谱(RP-HPLC)纯化获得标记物纯品14C-毒氟磷(N-2-(4-甲基苯并2-14C噻唑基)-2-氨基-2-氟代苯基-O,O-二乙基甲基膦酸酯,38.3 mCi)。7步反应的化学收率/放化收率为10%。其结构经核磁共振氢谱、质谱和放射性高效液相色谱(HPLC-FSA)分析确认。放射性薄层成像分析(TLC-IIA)、高效液相色谱-液体闪烁测量联用分析(HPLC-LSC)、高效液相色谱-流动液体闪烁测量/二极管阵列检测器/质谱联用分析(HPLC-FSA/PDA/MS)和LSC分析表明,14C-毒氟磷的放化纯度和化学纯度均大于98%,比活度为58.0 mCi/mmol,可作为放射性示踪剂,用于毒氟磷的代谢和环境行为等研究。

       

      Abstract: Carbon-14 labelled Dufulin, diethyl ((2-fluorophenyl)((4-methylbenzo2-14Cthiazol-2-yl) amino)methyl)phosphonate was synthesized from barium 14Ccarbonate via Grignard reaction, Curtius arrangement, nucleophilic addition, thionation reaction, cyclization reaction, etc. The labelled product (38.3 mCi) was obtained after RP-HPLC purification in the overall radiochemical/chemical yield of 10%. The product was characterized by ESI-MS, 1H NMR and HPLC-FSA. Its technical data (radiochemical purity > 98%, chemical purity > 98%, specific activity 58.0 mCi/mmol) was determined by TLC-IIA, HPLC-LSC, HPLC-FSA/PDA/MS and LSC. This carbon-14 labelled Dufulin can be used as radiotracer in the study on its metabolism and environmental behavior by employing radioisotope tracing techniques.

       

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