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Synthesis of the calcilytic ligand NPS 2143

(R)-3 (NPS 2143) is a negative allosteric modulator of the human calcium-sensing receptor (CaSR) and as such represents an important pharmacological tool compound for studying the CaSR. Herein, we disclose for the first time a complete experimental description, detailed characterisation and assessme...

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Autores principales: Johansson, Henrik, Cailly, Thomas, Rojas Bie Thomsen, Alex, Bräuner-Osborne, Hans, Sejer Pedersen, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3740522/
https://www.ncbi.nlm.nih.gov/pubmed/23946832
http://dx.doi.org/10.3762/bjoc.9.154
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author Johansson, Henrik
Cailly, Thomas
Rojas Bie Thomsen, Alex
Bräuner-Osborne, Hans
Sejer Pedersen, Daniel
author_facet Johansson, Henrik
Cailly, Thomas
Rojas Bie Thomsen, Alex
Bräuner-Osborne, Hans
Sejer Pedersen, Daniel
author_sort Johansson, Henrik
collection PubMed
description (R)-3 (NPS 2143) is a negative allosteric modulator of the human calcium-sensing receptor (CaSR) and as such represents an important pharmacological tool compound for studying the CaSR. Herein, we disclose for the first time a complete experimental description, detailed characterisation and assessment of enantiomeric purity for (R)-3. An efficient, reproducible and scalable synthesis of (R)-3 that requires a minimum of chromatographic purification steps is presented. (R)-3 was obtained in excellent optical purity (er > 99:1) as demonstrated by chiral HPLC and the pharmacological profile for (R)-3 is in full accordance with that reported in the literature.
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spelling pubmed-37405222013-08-14 Synthesis of the calcilytic ligand NPS 2143 Johansson, Henrik Cailly, Thomas Rojas Bie Thomsen, Alex Bräuner-Osborne, Hans Sejer Pedersen, Daniel Beilstein J Org Chem Full Research Paper (R)-3 (NPS 2143) is a negative allosteric modulator of the human calcium-sensing receptor (CaSR) and as such represents an important pharmacological tool compound for studying the CaSR. Herein, we disclose for the first time a complete experimental description, detailed characterisation and assessment of enantiomeric purity for (R)-3. An efficient, reproducible and scalable synthesis of (R)-3 that requires a minimum of chromatographic purification steps is presented. (R)-3 was obtained in excellent optical purity (er > 99:1) as demonstrated by chiral HPLC and the pharmacological profile for (R)-3 is in full accordance with that reported in the literature. Beilstein-Institut 2013-07-09 /pmc/articles/PMC3740522/ /pubmed/23946832 http://dx.doi.org/10.3762/bjoc.9.154 Text en Copyright © 2013, Johansson et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Johansson, Henrik
Cailly, Thomas
Rojas Bie Thomsen, Alex
Bräuner-Osborne, Hans
Sejer Pedersen, Daniel
Synthesis of the calcilytic ligand NPS 2143
title Synthesis of the calcilytic ligand NPS 2143
title_full Synthesis of the calcilytic ligand NPS 2143
title_fullStr Synthesis of the calcilytic ligand NPS 2143
title_full_unstemmed Synthesis of the calcilytic ligand NPS 2143
title_short Synthesis of the calcilytic ligand NPS 2143
title_sort synthesis of the calcilytic ligand nps 2143
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3740522/
https://www.ncbi.nlm.nih.gov/pubmed/23946832
http://dx.doi.org/10.3762/bjoc.9.154
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