Investigation of the role of the base in the synthesis of [18F]FLT.

TitleInvestigation of the role of the base in the synthesis of [18F]FLT.
Publication TypeJournal Article
Year of Publication2007
AuthorsSuehiro M, Vallabhajosula S, Goldsmith SJ, Ballon DJ
JournalAppl Radiat Isot
Volume65
Issue12
Pagination1350-8
Date Published2007 Dec
ISSN0969-8043
KeywordsAnimals, Chromatography, High Pressure Liquid, Dideoxynucleosides, Fluorine Radioisotopes, Humans, Molecular Structure, Positron-Emission Tomography, Radiopharmaceuticals
Abstract

The role of the base in the synthesis of 3'-deoxy-3'-[18F]fluorothymidine, [18F]FLT, via nucleophilic substitution of the nosyl group with [18F]fluoride was investigated. The rate of 18F-incorporation into the molecule dramatically changed as a function of the precursor-to-base ratio. In the presence of excess base, the precursor was consumed by elimination before substitution was complete. When the precursor-to-base ratio was optimal, an overall [18F]FLT yield of 30-40% was achieved even if the precursor amount was as small as 8-13 mg.

DOI10.1016/j.apradiso.2007.07.013
Alternate JournalAppl Radiat Isot
PubMed ID17919915
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065