A rapid microfluidic synthesis of [18F]fluoroarenes from nitroarenes

被引:7
|
作者
Moore, Thomas M.
Akula, Murthy R.
Collier, Lee
Kabalka, George W. [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
Radiofluorination; Fluordenitration; Aromatic Fluorinatio; Microfluidics; Automation;
D O I
10.1016/j.apradiso.2012.09.013
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Microfluidic radiofluorodenitrations have been successfully performed using a commercially available microfluidic synthesis system. Reactions of nitroarenes with para-substituted electron withdrawing groups provide incorporation yields ranging from 43 to 97%. Ortho- and meta-substituted nitroarenes provided incorporation yields up to 35%. The reactions were conducted using dry, no-carrier-added [F-18]-fluoride and K2CO3/K-222 dissolved in N,N-dimethylformamide or dimethyl sulfoxide with total synthesis times of less than five min. The methodology developed in these studies can be applied to the synthesis of a variety of fluorine-18 labeled radiotracers and radiolabeled prosthetic groups from nitroarene precursors. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:47 / 50
页数:4
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