Radiosynthesis and reactivity of N-[11C]methyl carbamoylimidazole.
Authors
Kadirvel, Manikandan
Cardoso, Déborah
Freeman, Sally
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Abstract
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-[11C]methyl carbamoylimidazole as a new [11C]synthon to radiolabel biomolecules for PET imaging research. N-[11C]methyl carbamoylimidazole was prepared from [11C]methyl iodide in 70-74% radiochemical yield (decay corrected) and can be used in situ for further reaction without purification. The reactivity of N-[11C]methyl carbamoylimidazole was demonstrated in a series of [11C]carbamoylation reactions.
Publication Date
2018
Online Publication Date
2018-06-19
Acceptance Date
Keywords
11C, Carbamoylation, Methyl isocyanate, PET, Radiochemistry
Journal Title
J Radioanal Nucl Chem
Journal ISSN
0236-5731
1588-2780
1588-2780
Volume Title
317
Publisher
Springer Science and Business Media LLC