(E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol

In the title compound, C(20)H(27)N(3)O, the hy­droxy group forms an intra­molecular O—H⋯N hydrogen bond with the imino N atom. The dihedral angle between the aromatic rings is 33.09 (9)°. In the crystal, mol­ecules form centrosymmetric dimers via pairs of N—H⋯N hydrogen bonds involving amino­pyridin...

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Detalles Bibliográficos
Autores principales: Carreño, Alexander, Ladeira, Sonia, Castel, Annie, Vega, Andres, Chavez, Ivonne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414959/
https://www.ncbi.nlm.nih.gov/pubmed/22904946
http://dx.doi.org/10.1107/S1600536812032060
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author Carreño, Alexander
Ladeira, Sonia
Castel, Annie
Vega, Andres
Chavez, Ivonne
author_facet Carreño, Alexander
Ladeira, Sonia
Castel, Annie
Vega, Andres
Chavez, Ivonne
author_sort Carreño, Alexander
collection PubMed
description In the title compound, C(20)H(27)N(3)O, the hy­droxy group forms an intra­molecular O—H⋯N hydrogen bond with the imino N atom. The dihedral angle between the aromatic rings is 33.09 (9)°. In the crystal, mol­ecules form centrosymmetric dimers via pairs of N—H⋯N hydrogen bonds involving amino­pyridine fragments.
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spelling pubmed-34149592012-08-17 (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol Carreño, Alexander Ladeira, Sonia Castel, Annie Vega, Andres Chavez, Ivonne Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(27)N(3)O, the hy­droxy group forms an intra­molecular O—H⋯N hydrogen bond with the imino N atom. The dihedral angle between the aromatic rings is 33.09 (9)°. In the crystal, mol­ecules form centrosymmetric dimers via pairs of N—H⋯N hydrogen bonds involving amino­pyridine fragments. International Union of Crystallography 2012-07-21 /pmc/articles/PMC3414959/ /pubmed/22904946 http://dx.doi.org/10.1107/S1600536812032060 Text en © Carreño et al. 2012 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
Carreño, Alexander
Ladeira, Sonia
Castel, Annie
Vega, Andres
Chavez, Ivonne
(E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title_full (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title_fullStr (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title_full_unstemmed (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title_short (E)-2-{[(2-Amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
title_sort (e)-2-{[(2-amino­pyridin-3-yl)imino]­meth­yl}-4,6-di-tert-butyl­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414959/
https://www.ncbi.nlm.nih.gov/pubmed/22904946
http://dx.doi.org/10.1107/S1600536812032060
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