Rapid microwave-assisted fluorination yielding novel 5′-deoxy-5′-fluorouridine derivatives

A rapid fluorination at the 5′-position of nucleosides derivatives is achieved within 45 min providing yields of 75–92% by application of microwave. The preparation of 18F-labeled ligands for positron emission tomography (PET) and the subsequent imaging have to be completed within a half-life of the...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2006-12, Vol.16 (23), p.6139-6142
Hauptverfasser: Le, H. Phuoc, Müller, Christa E.
Format: Artikel
Sprache:eng
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Zusammenfassung:A rapid fluorination at the 5′-position of nucleosides derivatives is achieved within 45 min providing yields of 75–92% by application of microwave. The preparation of 18F-labeled ligands for positron emission tomography (PET) and the subsequent imaging have to be completed within a half-life of the neutron-deficient isotope ( 18F = 110 min). In this paper, we report a rapid fluorination approach to obtain 5′-deoxy-5′-fluoro-substituted uracil nucleoside analogues. Nucleophilic substitution at the 5′-position of the nucleosides was achieved within 45 min providing excellent yields of 75–92% by application of microwaves.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2006.08.093