Methyl N-(3-cyano­picolino­yl)-l-tryptophanate

In the title compound, C(19)H(16)N(4)O(3), the stereocenter has an l configuration; l-tryptophan methyl ester hydro­chloride being used as a starting material. The indole ring system and the pyridine ring are inclined to one another by 13.55 (14)°. In the crystal, adjacent mol­ecules are linked via...

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Autores principales: Ovdiichuk, Olga, Hordiyenko, Olga, Voitenko, Zoia, Arrault, Axelle, Medviediev, Volodymyr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885065/
https://www.ncbi.nlm.nih.gov/pubmed/24454241
http://dx.doi.org/10.1107/S160053681303153X
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author Ovdiichuk, Olga
Hordiyenko, Olga
Voitenko, Zoia
Arrault, Axelle
Medviediev, Volodymyr
author_facet Ovdiichuk, Olga
Hordiyenko, Olga
Voitenko, Zoia
Arrault, Axelle
Medviediev, Volodymyr
author_sort Ovdiichuk, Olga
collection PubMed
description In the title compound, C(19)H(16)N(4)O(3), the stereocenter has an l configuration; l-tryptophan methyl ester hydro­chloride being used as a starting material. The indole ring system and the pyridine ring are inclined to one another by 13.55 (14)°. In the crystal, adjacent mol­ecules are linked via N—H⋯O hydrogen bonds, forming chains propagating along the c-axis direction.
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spelling pubmed-38850652014-01-17 Methyl N-(3-cyano­picolino­yl)-l-tryptophanate Ovdiichuk, Olga Hordiyenko, Olga Voitenko, Zoia Arrault, Axelle Medviediev, Volodymyr Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(16)N(4)O(3), the stereocenter has an l configuration; l-tryptophan methyl ester hydro­chloride being used as a starting material. The indole ring system and the pyridine ring are inclined to one another by 13.55 (14)°. In the crystal, adjacent mol­ecules are linked via N—H⋯O hydrogen bonds, forming chains propagating along the c-axis direction. International Union of Crystallography 2013-11-23 /pmc/articles/PMC3885065/ /pubmed/24454241 http://dx.doi.org/10.1107/S160053681303153X Text en © Ovdiichuk et al. 2013 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 Organic Papers
Ovdiichuk, Olga
Hordiyenko, Olga
Voitenko, Zoia
Arrault, Axelle
Medviediev, Volodymyr
Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title_full Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title_fullStr Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title_full_unstemmed Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title_short Methyl N-(3-cyano­picolino­yl)-l-tryptophanate
title_sort methyl n-(3-cyano­picolino­yl)-l-tryptophanate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885065/
https://www.ncbi.nlm.nih.gov/pubmed/24454241
http://dx.doi.org/10.1107/S160053681303153X
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AT arraultaxelle methyln3cyanopicolinoylltryptophanate
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