Synthesis of [18F]-labeled EF3 [2-(2-nitroimidazol-1-yl)-N-(3,3,3-trifluoropropyl)-acetamide], a marker for PET detection of hypoxia

被引:50
作者
Josse, O
Labar, D
Georges, B
Grégoire, V
Marchand-Brynaert, J
机构
[1] Univ Catholique Louvain, Unite Chim Organ & Med, B-1348 Louvain, Belgium
[2] Univ Catholique Louvain, Lab Tomog Positron, B-1348 Louvain, Belgium
[3] Univ Catholique Louvain, Hop Univ St Luc, Radiobiol Lab, B-1200 Brussels, Belgium
关键词
D O I
10.1016/S0968-0896(00)00279-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[F-18]-2-(2-Nitroimidazol-1-yl)-N-(3,3,3-trifluoropropyl)-acetamide ([F-18]-EF3) has been prepared, in 65% chemical yield and 5% radiochemical yield, by coupling 2,3,5,6-tetrafluorophenyl 2-(2-nitroimidazol-1-yl) acetate 1 with [F-18]-3,3,3-trifluoropropylamine 7. This original radiolabelled key-synthon was obtained in 40% overall chemical yield by oxidative [F-18]-fluorodesulfurization of ethyl N-phthalimido-3-aminopropane dithioate 4, followed by deprotection with hydrazine of the resulting [F-18]-N-phthalimido-3,3,3-trifluoropropylamine 5. All the process was performed within 90 min, from the [F-18]-HF production in the cyclotron to the purification of the final target. (C) 2001 Elsevier Science Ltd. All rights reserved.
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页码:665 / 675
页数:11
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