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5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole

In the title compound, C(25)H(22)N(2)O(2), the indole rings are individually almost planar [with maximum deviations of 0.0116 (19) and 0.0113 (18) Å] and are almost orthogonal to each other, making a dihedral angle of 84.49 (6)°. The benzene ring is inclined at 72.83 (9) and 80.85 (9)° with respect...

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Autores principales: Narayanan, P., Sethusankar, K., Ramachandiran, K., Perumal, P. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238863/
https://www.ncbi.nlm.nih.gov/pubmed/22199716
http://dx.doi.org/10.1107/S1600536811045491
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author Narayanan, P.
Sethusankar, K.
Ramachandiran, K.
Perumal, P. T.
author_facet Narayanan, P.
Sethusankar, K.
Ramachandiran, K.
Perumal, P. T.
author_sort Narayanan, P.
collection PubMed
description In the title compound, C(25)H(22)N(2)O(2), the indole rings are individually almost planar [with maximum deviations of 0.0116 (19) and 0.0113 (18) Å] and are almost orthogonal to each other, making a dihedral angle of 84.49 (6)°. The benzene ring is inclined at 72.83 (9) and 80.85 (9)° with respect to the indole rings. In the crystal, mol­ecules are linked by N—H⋯O inter­actions into chains running parallel to the c axis. The crystal structure is further stabilized by C—H⋯π inter­actions.
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spelling pubmed-32388632011-12-23 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole Narayanan, P. Sethusankar, K. Ramachandiran, K. Perumal, P. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(22)N(2)O(2), the indole rings are individually almost planar [with maximum deviations of 0.0116 (19) and 0.0113 (18) Å] and are almost orthogonal to each other, making a dihedral angle of 84.49 (6)°. The benzene ring is inclined at 72.83 (9) and 80.85 (9)° with respect to the indole rings. In the crystal, mol­ecules are linked by N—H⋯O inter­actions into chains running parallel to the c axis. The crystal structure is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2011-11-05 /pmc/articles/PMC3238863/ /pubmed/22199716 http://dx.doi.org/10.1107/S1600536811045491 Text en © Narayanan et al. 2011 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
Narayanan, P.
Sethusankar, K.
Ramachandiran, K.
Perumal, P. T.
5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title_full 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title_fullStr 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title_full_unstemmed 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title_short 5-Meth­oxy-3-[(5-meth­oxy-1H-indol-3-yl)(phen­yl)meth­yl]-1H-indole
title_sort 5-meth­oxy-3-[(5-meth­oxy-1h-indol-3-yl)(phen­yl)meth­yl]-1h-indole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238863/
https://www.ncbi.nlm.nih.gov/pubmed/22199716
http://dx.doi.org/10.1107/S1600536811045491
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