6-~(18)F氟-L-多巴的合成
SYNTHESIS OF 6-~(18)FFLUORO-L-DOPA
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摘要: 以硝基藜芦醛为原料 ,采用亲核取代合成法 ,利用手性相转移催化烷基化等多步反应制备了6 18F氟 L 多巴 (18FDOPA) ,并用手性流动相和反相C18柱的HPLC法测定对映纯度。结果表明 ,18FDOPA总的合成时间少于 12 0min ,经衰减校正后总放化产额约为 6 3% ,对映纯度和放化纯度分别大于 95 %和 99%Abstract: FFluoro L dopa ( 18 FDOPA) is synthesized from the starting material nitro vera traldehyde via multi step reaction by nucleophilic displacement combined with chiral catalytic phase transfer alkylation techniques and the enantiomeric purity of 18 FDOPA is determined by HPLC method using a chiral mobil phase and reversed phase C18 column. The results show that the total time of synthesis is less than 120 min, the total radiochemical yield from potassium 18 F fluoride is about 6.3 % with decay correction and the enantiomeric purity and radiochemical purity are high than 95 % and 99 %, respectively. The practical techniques are provided for the radiochemical synthesis and entiomeric purity determination of 18 FDOPA and other 18 Ffluoro L amino acids.