N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide

In the title compound, C(21)H(24)N(4)O(2), inversion-related mol­ecules are linked into dimers through pairs of N—H⋯O hydrogen bonds, which generate R (2) (2)(8) motifs. As well as dimer formation, an additional N—H⋯O hydrogen bond and two C—H⋯π contacts, involving H atoms from the phenyl ring and t...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohamed, Shaaban K., Horton, Peter N., Akkurt, Mehmet, Albayati, Mustafa R., Abdelhamid, Antar A.
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/PMC3393912/
https://www.ncbi.nlm.nih.gov/pubmed/22798777
http://dx.doi.org/10.1107/S1600536812026013
_version_ 1782237780312588288
author Mohamed, Shaaban K.
Horton, Peter N.
Akkurt, Mehmet
Albayati, Mustafa R.
Abdelhamid, Antar A.
author_facet Mohamed, Shaaban K.
Horton, Peter N.
Akkurt, Mehmet
Albayati, Mustafa R.
Abdelhamid, Antar A.
author_sort Mohamed, Shaaban K.
collection PubMed
description In the title compound, C(21)H(24)N(4)O(2), inversion-related mol­ecules are linked into dimers through pairs of N—H⋯O hydrogen bonds, which generate R (2) (2)(8) motifs. As well as dimer formation, an additional N—H⋯O hydrogen bond and two C—H⋯π contacts, involving H atoms from the phenyl ring and the pyrrole and benzene rings of the indole system, generate a three-dimensional network.
format Online
Article
Text
id pubmed-3393912
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-33939122012-07-13 N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide Mohamed, Shaaban K. Horton, Peter N. Akkurt, Mehmet Albayati, Mustafa R. Abdelhamid, Antar A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(24)N(4)O(2), inversion-related mol­ecules are linked into dimers through pairs of N—H⋯O hydrogen bonds, which generate R (2) (2)(8) motifs. As well as dimer formation, an additional N—H⋯O hydrogen bond and two C—H⋯π contacts, involving H atoms from the phenyl ring and the pyrrole and benzene rings of the indole system, generate a three-dimensional network. International Union of Crystallography 2012-06-13 /pmc/articles/PMC3393912/ /pubmed/22798777 http://dx.doi.org/10.1107/S1600536812026013 Text en © Mohamed 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
Mohamed, Shaaban K.
Horton, Peter N.
Akkurt, Mehmet
Albayati, Mustafa R.
Abdelhamid, Antar A.
N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title_full N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title_fullStr N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title_full_unstemmed N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title_short N′-[(E)-4-(Dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1H-indol-3-yl)acetohydrazide
title_sort n′-[(e)-4-(dimethyl­amino)­benz­ylidene]-2-(5-meth­oxy-2-methyl-1h-indol-3-yl)acetohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393912/
https://www.ncbi.nlm.nih.gov/pubmed/22798777
http://dx.doi.org/10.1107/S1600536812026013
work_keys_str_mv AT mohamedshaabank ne4dimethylaminobenzylidene25methoxy2methyl1hindol3ylacetohydrazide
AT hortonpetern ne4dimethylaminobenzylidene25methoxy2methyl1hindol3ylacetohydrazide
AT akkurtmehmet ne4dimethylaminobenzylidene25methoxy2methyl1hindol3ylacetohydrazide
AT albayatimustafar ne4dimethylaminobenzylidene25methoxy2methyl1hindol3ylacetohydrazide
AT abdelhamidantara ne4dimethylaminobenzylidene25methoxy2methyl1hindol3ylacetohydrazide

Ejemplares similares