Radiosynthesis and reactivity of N-[11C]methyl carbamoylimidazole

被引:2
|
作者
Kadirvel, Manikandan [1 ,2 ]
Cardoso, Deborah [3 ]
Freeman, Sally [2 ]
Brown, Gavin [4 ]
机构
[1] Univ Manchester, Wolfson Mol Imaging Ctr, Manchester M20 3LJ, Lancs, England
[2] Univ Manchester, Fac Biol Med & Hlth, Sch Hlth Sci, Div Pharm & Optometry, Manchester M13 9PT, Lancs, England
[3] Univ Auvergne, Fac Pharm, F-63000 Clermont Ferrand, France
[4] Univ Cambridge, Addenbrookes Hosp, Dept Clin Neurosci, Wolfson Brain Imaging Ctr, Box 65, Cambridge CB2 0QQ, England
关键词
C-11; Radiochemistry; PET; Methyl isocyanate; Carbamoylation; ALKYL CYANATES; METHYL ISOCYANATE;
D O I
10.1007/s10967-018-5948-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
N-Methyl carbamoylimidazole is a safe and practical alternative to methyl isocyanate for carbamoylation reactions. We have developed a new chemical route for its synthesis from methyl iodide and applied this to the synthesis of N-[C-11]methyl carbamoylimidazole as a new [C-11]synthon to radiolabel biomolecules for PET imaging research. N-[C-11]methyl carbamoylimidazole was prepared from [C-11]methyl iodide in 70-74% radiochemical yield (decay corrected) and can be used in situ for further reaction without purification. The reactivity of N-[C-11]methyl carbamoylimidazole was demonstrated in a series of [C-11]carbamoylation reactions.
引用
收藏
页码:977 / 984
页数:8
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