The synthesis of no-carrier-added [C-11]urea from [C-11]carbon dioxide and application to [C-11]uracil synthesis

被引:16
|
作者
Chakraborty, PK
Mangner, TJ
Chugani, HT
机构
[1] Children's Hospital of Michigan, Department of Pediatric Imaging, Wayne Stt. Univ. School of Medicine, Detroit
关键词
D O I
10.1016/S0969-8043(97)00007-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
No-carrier-added [C-11]urea has been synthesized by bubbling cyclotron-produced [C-11]carbon dioxide directly into a tetrahydrofuran solution of lithium bis(trimethylsilyl)amide, followed by hydrolysis of the C-11 labeled adduct with aqueous ammonium chloride. Using this simple, one-pot method, [C-11]urea was produced in 55-70% radiochemical yield (decay-corrected) in 16 min following end-of-bombardment (or in 10 min following the introduction of the [C-11]carbon dioxide). The [C-11]urea thus produced was converted to [C-11]uracil (carrier-added) in 40-75% decay-corrected radiochemical yield by condensation with diethyl malate in presence of fuming sulfuric acid. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:619 / 621
页数:3
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