## Abstract Fluorine‐18 labeled 1,1‐difluoro‐2,2‐dichloroethyl aryl ethers have been prepared by a facile ^18^F‐for‐^19^F isotopic exchange reaction. The isotopic exchange proceeds in good to excellent yields (up to 85%), and is dependent on reaction time, temperature, and concentration of reactant
[18F]/19F exchange in fluorine containing compounds for potential use in 18F-labelling strategies
✍ Scribed by Elisabeth Blom; Farhad Karimi; Bengt Långström
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 216 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Exchange of [^18^F]fluoride with ^19^F in various organofluorine compounds in concentrations ranging from 0.06 to 56 mM was explored. We aimed to explore whether exchange reactions can be a potential useful labelling strategy, when there are no requirement of high specific radioactivity. Parameters such as solvents, temperature, conventional vs microwave heating, and the degree of fluorine load in some aromatic and alkyl compounds were investigated with regard to radiochemical yield and specific radioactivity. A series of fluorobenzophenones (1–6), 1‐(4‐fluorophenyl)ethanone (7), various activated and deactivated fluoro benzenes (8–16), N‐(pentafluorophenyl)benzamide (17), (pentafluorophenyl)formamide (18), (tridecafluorohexyl)benzene (19) and tetradecafluorohexane (20) were subjected to [^18^F]/^19^F exchange. To test this strategy to label biologically active molecules containing fluorine atoms in an aryl group, two analogues of WAY‐100635 (21–22), Lapatinib (23), 2,5,6,7,8‐pentafluoro‐3‐methylnaphthoquinone (24) and 1‐(2,4‐difluorophenyl)‐3‐(4‐fluorophenyl)propan‐1‐one (25) were investigated. The multi‐fluorinated molecules containing an electron‐withdrawing group were successfully labelled at room temperature, whereas the monofluorinated, as well as those containing an electron‐donating group, required heating for the exchange reaction to take place. Copyright © 2009 John Wiley & Sons, Ltd.
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