Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate

In the mol­ecule of the title compound, C(22)H(17)ClN(2)O(2), the dihedral angles formed by the pyrrole ring with the quinoline and phenyl rings are 67.93 (8) and 28.40 (11)°, respectively. In the crystal structure, mol­ecules are linked into dimers by inter­molecular C—H⋯O hydrogen bonds....

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Detalles Bibliográficos
Autores principales: Benzerka, Saida, Bouraiou, Abdelmalek, Bouacida, Sofiane, Debache, Abdelmadjid, Belfaitah, Ali
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959760/
https://www.ncbi.nlm.nih.gov/pubmed/21580979
http://dx.doi.org/10.1107/S1600536808032546
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author Benzerka, Saida
Bouraiou, Abdelmalek
Bouacida, Sofiane
Debache, Abdelmadjid
Belfaitah, Ali
author_facet Benzerka, Saida
Bouraiou, Abdelmalek
Bouacida, Sofiane
Debache, Abdelmadjid
Belfaitah, Ali
author_sort Benzerka, Saida
collection PubMed
description In the mol­ecule of the title compound, C(22)H(17)ClN(2)O(2), the dihedral angles formed by the pyrrole ring with the quinoline and phenyl rings are 67.93 (8) and 28.40 (11)°, respectively. In the crystal structure, mol­ecules are linked into dimers by inter­molecular C—H⋯O hydrogen bonds.
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spelling pubmed-29597602010-12-30 Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate Benzerka, Saida Bouraiou, Abdelmalek Bouacida, Sofiane Debache, Abdelmadjid Belfaitah, Ali Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecule of the title compound, C(22)H(17)ClN(2)O(2), the dihedral angles formed by the pyrrole ring with the quinoline and phenyl rings are 67.93 (8) and 28.40 (11)°, respectively. In the crystal structure, mol­ecules are linked into dimers by inter­molecular C—H⋯O hydrogen bonds. International Union of Crystallography 2008-10-15 /pmc/articles/PMC2959760/ /pubmed/21580979 http://dx.doi.org/10.1107/S1600536808032546 Text en © Benzerka et al. 2008 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
Benzerka, Saida
Bouraiou, Abdelmalek
Bouacida, Sofiane
Debache, Abdelmadjid
Belfaitah, Ali
Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title_full Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title_fullStr Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title_full_unstemmed Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title_short Ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl­ate
title_sort ethyl 4-(2-chloro­quinolin-3-yl)-1-phenyl-1h-pyrrole-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959760/
https://www.ncbi.nlm.nih.gov/pubmed/21580979
http://dx.doi.org/10.1107/S1600536808032546
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AT debacheabdelmadjid ethyl42chloroquinolin3yl1phenyl1hpyrrole3carboxylate
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