N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine

In the crystal structure of the title compound, C(21)H(18)FN(5), the pyridopyrazine ring system forms dihedral angles of 33.27 (7) and 48.69 (9)° with the 4-fluoro­phenyl and pyridine ring, respectively. The dihedral angle of the 4-fluoro­phenyl and pyridine rings is 57.45 (8)°. The crystal packing...

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Detalles Bibliográficos
Autores principales: Koch, Pierre, Schollmeyer, Dieter, Laufer, Stefan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970374/
https://www.ncbi.nlm.nih.gov/pubmed/21577998
http://dx.doi.org/10.1107/S1600536809038173
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author Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_facet Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_sort Koch, Pierre
collection PubMed
description In the crystal structure of the title compound, C(21)H(18)FN(5), the pyridopyrazine ring system forms dihedral angles of 33.27 (7) and 48.69 (9)° with the 4-fluoro­phenyl and pyridine ring, respectively. The dihedral angle of the 4-fluoro­phenyl and pyridine rings is 57.45 (8)°. The crystal packing is characterized by an inter­molecular N—H⋯N hydrogen bond.
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spelling pubmed-29703742010-12-30 N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine Koch, Pierre Schollmeyer, Dieter Laufer, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(21)H(18)FN(5), the pyridopyrazine ring system forms dihedral angles of 33.27 (7) and 48.69 (9)° with the 4-fluoro­phenyl and pyridine ring, respectively. The dihedral angle of the 4-fluoro­phenyl and pyridine rings is 57.45 (8)°. The crystal packing is characterized by an inter­molecular N—H⋯N hydrogen bond. International Union of Crystallography 2009-09-26 /pmc/articles/PMC2970374/ /pubmed/21577998 http://dx.doi.org/10.1107/S1600536809038173 Text en © Koch et al. 2009 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
Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title_full N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title_fullStr N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title_full_unstemmed N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title_short N-{4-[3-(4-Fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
title_sort n-{4-[3-(4-fluoro­phen­yl)pyrido[2,3-b]pyrazin-2-yl]-2-pyrid­yl}isopropyl­amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970374/
https://www.ncbi.nlm.nih.gov/pubmed/21577998
http://dx.doi.org/10.1107/S1600536809038173
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AT schollmeyerdieter n434fluorophenylpyrido23bpyrazin2yl2pyridylisopropylamine
AT lauferstefan n434fluorophenylpyrido23bpyrazin2yl2pyridylisopropylamine

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