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

Published version
Peer-reviewed

Type

Article

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Authors

Kadirvel, Manikandan 
Cardoso, Déborah 
Freeman, Sally 

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.

Description

Keywords

11C, Carbamoylation, Methyl isocyanate, PET, Radiochemistry

Journal Title

J Radioanal Nucl Chem

Conference Name

Journal ISSN

0236-5731
1588-2780

Volume Title

317

Publisher

Springer Science and Business Media LLC