Convenient PET-tracer production via SuFEx 18 F-fluorination of nanomolar precursor amounts

Recently, a protocol for radiolabeling of aryl fluorosulfates ("SuFEx click radiolabeling") using ultrafast F/ F isotopic exchange has been reported. Although promising, the original procedure turned out to be rather inefficient. However, systematic optimization of the reaction parameters...

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Veröffentlicht in:European journal of medicinal chemistry 2022-07, Vol.237, p.114383
Hauptverfasser: Walter, Nils, Bertram, Jan, Drewes, Birte, Bahutski, Victor, Timmer, Marco, Schütz, Markus B, Krämer, Felicia, Neumaier, Felix, Endepols, Heike, Neumaier, Bernd, Zlatopolskiy, Boris D
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Sprache:eng
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Zusammenfassung:Recently, a protocol for radiolabeling of aryl fluorosulfates ("SuFEx click radiolabeling") using ultrafast F/ F isotopic exchange has been reported. Although promising, the original procedure turned out to be rather inefficient. However, systematic optimization of the reaction parameters allowed for development of a robust method for SuFEx radiolabeling which obviates the need for azeotropic drying, base addition and HPLC purification. The developed protocol enabled efficient F-fluorination of low nanomolar amounts of aryl fluorosulfates in highly diluted solution (micromolar concentrations). It was successfully used to prepare a series of 29 F-fluorosulfurylated phenols - including modified ezetimibe, α-tocopherol and etoposide, the two tyrosine derivatives Boc-Tyr([ F]FS)-OMe and H-Tyr([ F]FS)-OMe, the FAP-specific ligand [ F]FS-UAMC1110, and the DPA-714 analog [ F]FS-DPA - in fair to excellent yields. Preliminary evaluation demonstrated sufficient in vivo stability of radiofluorinated electron rich or neutral {Boc-Tyr([ F]FS)-OMe), H-Tyr([ F]FS)-OMe and [ F]FS-DPA} aryl fluorosulfates. Furthermore, [ F]FS-DPA was identified as a promising tracer for visualization of TSPO expression.
ISSN:1768-3254
DOI:10.1016/j.ejmech.2022.114383