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Fast and reliable method for the preparation of ortho- and para-[18F]fluorobenzyl halide derivatives: Key intermediates for the preparation of no-carrier-added PET aromatic radiopharmaceuticals
- Source :
-
Journal of Fluorine Chemistry . Jun2012, Vol. 138, p48-55. 8p. - Publication Year :
- 2012
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Abstract
- Abstract: A fast and reliable method suitable for the automated preparation of (substituted) [18F]fluorobenzyl halides from several [18F]fluorobenzaldehydes was developed. Aromatic nucleophilic substitution of trimethylammonium benzaldehyde triflate and nitro precursors was realized with no-carrier-added [18F]fluoride. After labeling, fluorine-18 containing aldehydes were trapped on a Solid Phase Extraction (SPE) cartridge and the subsequent conversion into benzyl halide was directly realized, on-line, on the support. Reduction of the aldehydes (>95%) was near-quantitative with an aqueous solution of NaBH4. Halogenation was performed on the same support with different aqueous solutions of concentrated acid (HI, HBr, HCl). The conversion of benzyl alcohols into [18F]fluorobenzyl halides (X=Cl, Br, I) usually proceeded within 2min at high yields. The halogenation proceeded at room temperature, with the exception of the 2-[18F]fluoro-3-methoxybenzyl, 2- and 4-[18F]fluorobenzyl halides, which required the use of HBr/HOAc (33%). With this method, various [18F]fluorobenzyl chloride, bromide and iodide compounds were obtained with high radiochemical purities (>90%) and with overall radiochemical yields of 15–70%. The radiosynthesis was completed in 30 or 45min from EOB, starting from the ammonium or nitro precursor, respectively. By using the same solid support, 2- and 4-[18F]fluorobenzyl bromide and iodide derivatives were near-quantitatively converted (>95%) into the corresponding azido compounds (60°C, 5min). As the reduction and halogenation steps were performed on solid supports, automation of the whole synthesis was straightforward. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 00221139
- Volume :
- 138
- Database :
- Academic Search Index
- Journal :
- Journal of Fluorine Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 74678298
- Full Text :
- https://doi.org/10.1016/j.jfluchem.2012.03.015