Faculty of Medicine and University Hospital Cologne, Institute of Radiochemistry and Experimental Molecular Imaging, University of Cologne, Kerpener Straße 62, 50937, Cologne, Germany.
Institute of Neuroscience and Medicine, Nuclear Chemistry (INM-5), Forschungszentrum Jülich GmbH, Wilhelm-Johnen-Straße, 52428, Jülich, Germany.
Chemistry. 2023 Jan 9;29(2):e202202965. doi: 10.1002/chem.202202965. Epub 2022 Nov 17.
Cu-mediated radiofluorination is a versatile tool for the preparation of F-labeled (hetero)aromatics. In this work, we systematically evaluated a series of complexes and identified several generally applicable mediators for highly efficient radiofluorination of aryl boronic and stannyl substrates. Utilization of these mediators in nBuOH/DMI or DMI significantly improved F-labeling yields despite use of lower precursor amounts. Impressively, application of 2.5 μmol aryl boronic acids was sufficient to achieve F-labeling yields of up to 75 %. The practicality of the novel mediators was demonstrated by efficient production of five PET-tracers and transfer of the method to an automated radiosynthesis module. In addition, (S)-3-[ F]FPhe and 6-[ F]FDOPA were prepared in activity yields of 23±1 % and 30±3 % using only 2.5 μmol of the corresponding boronic acid or trimethylstannyl precursor.
铜介导的放射性氟化是制备 F 标记(杂)芳基化合物的一种通用工具。在这项工作中,我们系统地评估了一系列配合物,并确定了几种可普遍适用于高效芳基硼酸和锡基底物放射性氟化的通用介导物。尽管使用的前体数量较少,但在 nBuOH/DMI 或 DMI 中使用这些介导物可显著提高 F 标记产率。令人印象深刻的是,应用 2.5μmol 的芳基硼酸足以实现高达 75%的 F 标记产率。通过高效制备五种 PET 示踪剂和将该方法转移到自动化放射性合成模块,证明了新型介导物的实用性。此外,仅使用 2.5μmol 的相应硼酸或三甲基锡基前体,即可以 23±1%和 30±3%的活性产率制备(S)-3-[ F]FPhe 和 6-[ F]FDOPA。