N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide

The asymmetric unit of the title compound, C23H23N3O2, contains two molecules in both of which, one amide N atom is in a syn position with respect to the pyridine N atom, while the other amide N atom is in an anti position (the syn--anti conformation). There are minor conformational differences betw...

Full description

Bibliographic Details
Main Authors: Blanka Klepetářová, Emanuel Makrlík, Vasily A. Babain, Václav Kašička
Format: Article
Language:English
Published: International Union of Crystallography 2012-04-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536812009026
id doaj-863dd8c0d2064d038883a480f93f0d47
record_format Article
spelling doaj-863dd8c0d2064d038883a480f93f0d472020-11-25T01:11:09ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-04-01684o1099o110010.1107/S1600536812009026N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamideBlanka KlepetářováEmanuel MakrlíkVasily A. BabainVáclav KašičkaThe asymmetric unit of the title compound, C23H23N3O2, contains two molecules in both of which, one amide N atom is in a syn position with respect to the pyridine N atom, while the other amide N atom is in an anti position (the syn--anti conformation). There are minor conformational differences between the two molecules, as reflected in the Npyridine—C—C—Namide torsion angles of −44.9 (3) and 136.0 (2)° for one molecule and 43.5 (3) and −131.1 (2)° for the other molecule. However, the two molecules show significant differences in the orientation of an ethyl group, with corresponding C—C—N—C torsion angles of 86.6 (3)° for one molecule and 79.6 (3)° for the other molecule. In the crystal, molecules are linked by weak C—H...O hydrogen bonds, forming a three-dimensional supramolecular network.http://scripts.iucr.org/cgi-bin/paper?S1600536812009026
collection DOAJ
language English
format Article
sources DOAJ
author Blanka Klepetářová
Emanuel Makrlík
Vasily A. Babain
Václav Kašička
spellingShingle Blanka Klepetářová
Emanuel Makrlík
Vasily A. Babain
Václav Kašička
N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
Acta Crystallographica Section E
author_facet Blanka Klepetářová
Emanuel Makrlík
Vasily A. Babain
Václav Kašička
author_sort Blanka Klepetářová
title N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
title_short N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
title_full N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
title_fullStr N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
title_full_unstemmed N,N′-Diethyl-N,N′-diphenylpyridine-2,6-dicarboxamide
title_sort n,n′-diethyl-n,n′-diphenylpyridine-2,6-dicarboxamide
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2012-04-01
description The asymmetric unit of the title compound, C23H23N3O2, contains two molecules in both of which, one amide N atom is in a syn position with respect to the pyridine N atom, while the other amide N atom is in an anti position (the syn--anti conformation). There are minor conformational differences between the two molecules, as reflected in the Npyridine—C—C—Namide torsion angles of −44.9 (3) and 136.0 (2)° for one molecule and 43.5 (3) and −131.1 (2)° for the other molecule. However, the two molecules show significant differences in the orientation of an ethyl group, with corresponding C—C—N—C torsion angles of 86.6 (3)° for one molecule and 79.6 (3)° for the other molecule. In the crystal, molecules are linked by weak C—H...O hydrogen bonds, forming a three-dimensional supramolecular network.
url http://scripts.iucr.org/cgi-bin/paper?S1600536812009026
work_keys_str_mv AT blankaklepetamp225amp345ovamp225 nnamp8242diethylnnamp8242diphenylpyridine26dicarboxamide
AT emanuelmakrlamp237k nnamp8242diethylnnamp8242diphenylpyridine26dicarboxamide
AT vasilyababain nnamp8242diethylnnamp8242diphenylpyridine26dicarboxamide
AT vamp225clavkaamp353iamp269ka nnamp8242diethylnnamp8242diphenylpyridine26dicarboxamide
_version_ 1725172676385832960