(2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine

The title compound, C(18)H(24)N(4), resides on a crystallographic inversion centre, so that the asymmetric unit comprises one half-mol­ecule. The piperazine ring adopts a chair conformation, with the mean planes of the two equatorial pyridine rings parallel to each other and separated by 2.54 (3) Å....

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Detalles Bibliográficos
Autores principales: Goh, Christopher, Morris, Lilliana S., Girouard, Michael P., Chidanguro, Tamuka, Jasinski, Jerry P.
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/PMC3770377/
https://www.ncbi.nlm.nih.gov/pubmed/24046662
http://dx.doi.org/10.1107/S160053681301605X
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author Goh, Christopher
Morris, Lilliana S.
Girouard, Michael P.
Chidanguro, Tamuka
Jasinski, Jerry P.
author_facet Goh, Christopher
Morris, Lilliana S.
Girouard, Michael P.
Chidanguro, Tamuka
Jasinski, Jerry P.
author_sort Goh, Christopher
collection PubMed
description The title compound, C(18)H(24)N(4), resides on a crystallographic inversion centre, so that the asymmetric unit comprises one half-mol­ecule. The piperazine ring adopts a chair conformation, with the mean planes of the two equatorial pyridine rings parallel to each other and separated by 2.54 (3) Å. No classical hydrogen bonds are observed.
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spelling pubmed-37703772013-09-17 (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine Goh, Christopher Morris, Lilliana S. Girouard, Michael P. Chidanguro, Tamuka Jasinski, Jerry P. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(24)N(4), resides on a crystallographic inversion centre, so that the asymmetric unit comprises one half-mol­ecule. The piperazine ring adopts a chair conformation, with the mean planes of the two equatorial pyridine rings parallel to each other and separated by 2.54 (3) Å. No classical hydrogen bonds are observed. International Union of Crystallography 2013-06-15 /pmc/articles/PMC3770377/ /pubmed/24046662 http://dx.doi.org/10.1107/S160053681301605X Text en © Goh 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
Goh, Christopher
Morris, Lilliana S.
Girouard, Michael P.
Chidanguro, Tamuka
Jasinski, Jerry P.
(2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title_full (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title_fullStr (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title_full_unstemmed (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title_short (2S*,5R*)-2,5-Dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
title_sort (2s*,5r*)-2,5-dimethyl-1,4-bis­(pyridin-2-ylmeth­yl)piperazine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770377/
https://www.ncbi.nlm.nih.gov/pubmed/24046662
http://dx.doi.org/10.1107/S160053681301605X
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