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2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione

In the title compound, C(19)H(10)ClNO(4), the dihedral angle between the naphtho­quinone and coumarin rings is 48.99 (6)°. In the crystal, mol­ecules are linked by strong N—H⋯O hydrogen bonds into chains with graph-set motif C(6) along [101]. The packing also features π–π stacking inter­actions betw...

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Autores principales: Sousa, Mikaelly O. B., Silveira, Gleiciani Q., Gomez, Javier A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793804/
https://www.ncbi.nlm.nih.gov/pubmed/24109391
http://dx.doi.org/10.1107/S1600536813019922
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author Sousa, Mikaelly O. B.
Silveira, Gleiciani Q.
Gomez, Javier A. G.
author_facet Sousa, Mikaelly O. B.
Silveira, Gleiciani Q.
Gomez, Javier A. G.
author_sort Sousa, Mikaelly O. B.
collection PubMed
description In the title compound, C(19)H(10)ClNO(4), the dihedral angle between the naphtho­quinone and coumarin rings is 48.99 (6)°. In the crystal, mol­ecules are linked by strong N—H⋯O hydrogen bonds into chains with graph-set motif C(6) along [101]. The packing also features π–π stacking inter­actions between naphtho­quinone and coumarin rings [centroid-to-centroid distances = 3.7679 (12) and 3.6180 (13) Å].
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spelling pubmed-37938042013-10-09 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione Sousa, Mikaelly O. B. Silveira, Gleiciani Q. Gomez, Javier A. G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(10)ClNO(4), the dihedral angle between the naphtho­quinone and coumarin rings is 48.99 (6)°. In the crystal, mol­ecules are linked by strong N—H⋯O hydrogen bonds into chains with graph-set motif C(6) along [101]. The packing also features π–π stacking inter­actions between naphtho­quinone and coumarin rings [centroid-to-centroid distances = 3.7679 (12) and 3.6180 (13) Å]. International Union of Crystallography 2013-07-27 /pmc/articles/PMC3793804/ /pubmed/24109391 http://dx.doi.org/10.1107/S1600536813019922 Text en © Sousa et al. 2013 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
Sousa, Mikaelly O. B.
Silveira, Gleiciani Q.
Gomez, Javier A. G.
2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title_full 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title_fullStr 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title_full_unstemmed 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title_short 2-Chloro-3-[(2-oxo-2H-chromen-6-yl)amino]­naphthalene-1,4-dione
title_sort 2-chloro-3-[(2-oxo-2h-chromen-6-yl)amino]­naphthalene-1,4-dione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793804/
https://www.ncbi.nlm.nih.gov/pubmed/24109391
http://dx.doi.org/10.1107/S1600536813019922
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