A one-step automated high-radiochemical-yield synthesis of 18F-FECNT from mesylate precursor
2 β-Carbomethoxy-3 β-(4-chlorophenyl)-8-(2-[ 18F]fluoroethyl)nortropane ( 18F-FECNT) is a potential dopamine transporter imaging agent. In this article, a new mesylate precursor was prepared and a one-step automated synthesis of 18F-FECNT was developed. The mesylate precursor ( 4) was synthesized fr...
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Veröffentlicht in: | Applied radiation and isotopes 2008-12, Vol.66 (12), p.1881-1885 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 2
β-Carbomethoxy-3
β-(4-chlorophenyl)-8-(2-[
18F]fluoroethyl)nortropane (
18F-FECNT) is a potential dopamine transporter imaging agent. In this article, a new mesylate precursor was prepared and a one-step automated synthesis of
18F-FECNT was developed. The mesylate precursor (
4) was synthesized from 2
β-carbomethoxy-3
β-(4-chlorophenyl)tropane (
1) by
N-demethylation, hydroxyethylation followed by mesylation at a total yield of 47%. [
18F]fluorination was performed by heating 4
mg mesylate precursor and K[
18F] in 1
ml acetonitrile at 90
°C for 20
min. The crude
18F-FECNT was obtained with a radiolabeling yield of 48%. After purification by preparative high performance liquid chromatography (HPLC), the final
18F-FECNT product was obtained with a radiochemical purity of 98.4% and a decay corrected radiochemical yield of 33±9% (and the uncorrected radiochemical yield was 19±5%,
n=5). The duration of the total procedure was 80–90
min. |
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ISSN: | 0969-8043 1872-9800 |
DOI: | 10.1016/j.apradiso.2008.05.002 |