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Radiosynthesis and reactivity of N-[11C]methyl carbamoylimidazole.
Kadirvel, Manikandan; Cardoso, Déborah; Freeman, Sally; Brown, Gavin.
Afiliação
  • Kadirvel M; 1Wolfson Molecular Imaging Centre, University of Manchester, Manchester, M20 3LJ UK.
  • Cardoso D; 2Division of Pharmacy & Optometry, School of Health Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, M13 9PT UK.
  • Freeman S; 3Faculté de Pharmacie, Université d'Auvergne, 63000 Clermont-Ferrand, France.
  • Brown G; 2Division of Pharmacy & Optometry, School of Health Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, M13 9PT UK.
J Radioanal Nucl Chem ; 317(2): 977-984, 2018.
Article em En | MEDLINE | ID: mdl-30100651
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.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Radioanal Nucl Chem Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Radioanal Nucl Chem Ano de publicação: 2018 Tipo de documento: Article