Simple and efficient synthesis of 2-[18F]fluoroethyl triflate for high yield 18fluoroethylation

被引:4
|
作者
Peters, Tanja [1 ]
Vogg, Andreas [1 ]
Oppel, Iris M. [2 ]
Schmaljohann, Joern [1 ]
机构
[1] Rhein Westfal TH Aachen, Dept Nucl Med, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Dept Inorgan Chem, D-52074 Aachen, Germany
关键词
2-[F-18]fluoroethyl triflate; 2-[F-18]fluoroethanol; F-18-fluoroethylation; Fluorine-18; BIODISTRIBUTION;
D O I
10.1016/j.apradiso.2014.07.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The [F-18]fluoroethyl moiety has been widely utilized in the synthesis of F-18-labelled compounds. The aim of this work was the reliable synthesis of [F-18]FEtOTf with a novel strategy to increase the reactivity of the commonly used [F-18]FEB and [F-18]FEtOTos. [F-18]FEtOTf and the intermediate [F-18]FEtOH were synthesized in high RCY (78% and 85%, respectively) and purified by SPE. The high potency of [F-18] FEtOTf was shown by the efficient alkylation of the deactivated nucleophile aniline under mild conditions, as well as by the synthesis of [F-18]FEC. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:141 / 146
页数:6
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