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Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman

The title compound, C(11)H(11)FO(2), is a building block in the synthesis of the active pharmaceutical ingredient dl-nebivolol. The synthesis starting from the enanti­omerically pure (R)-6-fluoro-4-oxo-3,4-di­hydro-2H-chromene-2-carb­oxy­lic acid resulted in a mixture of two stereoisomers, namely (R...

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Autores principales: Rousselin, Yoann, Laureano, Hugo, Clavel, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571392/
https://www.ncbi.nlm.nih.gov/pubmed/26396792
http://dx.doi.org/10.1107/S205698901501261X
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author Rousselin, Yoann
Laureano, Hugo
Clavel, Alexandre
author_facet Rousselin, Yoann
Laureano, Hugo
Clavel, Alexandre
author_sort Rousselin, Yoann
collection PubMed
description The title compound, C(11)H(11)FO(2), is a building block in the synthesis of the active pharmaceutical ingredient dl-nebivolol. The synthesis starting from the enanti­omerically pure (R)-6-fluoro-4-oxo-3,4-di­hydro-2H-chromene-2-carb­oxy­lic acid resulted in a mixture of two stereoisomers, namely (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman and (R)-6-fluoro-2-[(R)-oxiran-2-yl]chroman. The mixture was separated by column chromatography but only one stereoisomer crystallized. The X-ray structure analysis revealed that the solid consisted of the R,S isomer. A similar procedure was repeated for (S)-6-fluoro-4-oxo-3,4-di­hydro-2H-chromene-2-carb­oxy­lic acid and, in this case, the S,R isomer was produced as a crystalline solid. Thus, all four stereoisomers of the title epoxide were obtained and their absolute configuration was assigned. The crystal studied was refined as an inversion twin.
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spelling pubmed-45713922015-09-22 Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman Rousselin, Yoann Laureano, Hugo Clavel, Alexandre Acta Crystallogr E Crystallogr Commun Data Reports The title compound, C(11)H(11)FO(2), is a building block in the synthesis of the active pharmaceutical ingredient dl-nebivolol. The synthesis starting from the enanti­omerically pure (R)-6-fluoro-4-oxo-3,4-di­hydro-2H-chromene-2-carb­oxy­lic acid resulted in a mixture of two stereoisomers, namely (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman and (R)-6-fluoro-2-[(R)-oxiran-2-yl]chroman. The mixture was separated by column chromatography but only one stereoisomer crystallized. The X-ray structure analysis revealed that the solid consisted of the R,S isomer. A similar procedure was repeated for (S)-6-fluoro-4-oxo-3,4-di­hydro-2H-chromene-2-carb­oxy­lic acid and, in this case, the S,R isomer was produced as a crystalline solid. Thus, all four stereoisomers of the title epoxide were obtained and their absolute configuration was assigned. The crystal studied was refined as an inversion twin. International Union of Crystallography 2015-07-08 /pmc/articles/PMC4571392/ /pubmed/26396792 http://dx.doi.org/10.1107/S205698901501261X Text en © Rousselin et al. 2015 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Rousselin, Yoann
Laureano, Hugo
Clavel, Alexandre
Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title_full Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title_fullStr Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title_full_unstemmed Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title_short Crystal structure of (R)-6-fluoro-2-[(S)-oxiran-2-yl]chroman
title_sort crystal structure of (r)-6-fluoro-2-[(s)-oxiran-2-yl]chroman
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571392/
https://www.ncbi.nlm.nih.gov/pubmed/26396792
http://dx.doi.org/10.1107/S205698901501261X
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