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The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives

Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelli...

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Autores principales: Blower, Julia E., Ma, Michelle T., Al-Salemee, Fahad A. I., Gee, Antony D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132178/
https://www.ncbi.nlm.nih.gov/pubmed/33876157
http://dx.doi.org/10.1039/d1cc00495f
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author Blower, Julia E.
Ma, Michelle T.
Al-Salemee, Fahad A. I.
Gee, Antony D.
author_facet Blower, Julia E.
Ma, Michelle T.
Al-Salemee, Fahad A. I.
Gee, Antony D.
author_sort Blower, Julia E.
collection PubMed
description Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelling strategies and tracers by adapting the multicomponent Hantzsch condensation reaction to prepare a library of (13)N-labelled 1,4-dihydropyridines from [(13)N]ammonia, including the widely-used drug nifedipine. This represents a key advance in (13)N PET radiochemistry, and will serve to underpin the renewed interest in clinical opportunities offered by short-lived PET tracers.
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spelling pubmed-81321782021-05-25 The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives Blower, Julia E. Ma, Michelle T. Al-Salemee, Fahad A. I. Gee, Antony D. Chem Commun (Camb) Chemistry Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelling strategies and tracers by adapting the multicomponent Hantzsch condensation reaction to prepare a library of (13)N-labelled 1,4-dihydropyridines from [(13)N]ammonia, including the widely-used drug nifedipine. This represents a key advance in (13)N PET radiochemistry, and will serve to underpin the renewed interest in clinical opportunities offered by short-lived PET tracers. The Royal Society of Chemistry 2021-04-08 /pmc/articles/PMC8132178/ /pubmed/33876157 http://dx.doi.org/10.1039/d1cc00495f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Blower, Julia E.
Ma, Michelle T.
Al-Salemee, Fahad A. I.
Gee, Antony D.
The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title_full The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title_fullStr The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title_full_unstemmed The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title_short The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
title_sort hantzsch reaction for nitrogen-13 pet: preparation of [(13)n]nifedipine and derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132178/
https://www.ncbi.nlm.nih.gov/pubmed/33876157
http://dx.doi.org/10.1039/d1cc00495f
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