Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate

The pyranyl ring of the title compound, C(22)H(19)NO(3), adopts a flattened-boat conformation. The dihedral angle between naphthalene and phenyl rings is 78.3 (1)°The mol­ecule also features an intra­molecular N—H⋯O(carbon­yl) hydrogen bond. Adjacent mol­ecules are linked by an inter­molecular N—H⋯O...

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Detalles Bibliográficos
Autores principales: Jiao, Yuan-Hong, Zhang, Qian, Meng, Fa-Yan, Teng, Lei, Yuan, Jia, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969098/
https://www.ncbi.nlm.nih.gov/pubmed/21582501
http://dx.doi.org/10.1107/S1600536809008885
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author Jiao, Yuan-Hong
Zhang, Qian
Meng, Fa-Yan
Teng, Lei
Yuan, Jia
Ng, Seik Weng
author_facet Jiao, Yuan-Hong
Zhang, Qian
Meng, Fa-Yan
Teng, Lei
Yuan, Jia
Ng, Seik Weng
author_sort Jiao, Yuan-Hong
collection PubMed
description The pyranyl ring of the title compound, C(22)H(19)NO(3), adopts a flattened-boat conformation. The dihedral angle between naphthalene and phenyl rings is 78.3 (1)°The mol­ecule also features an intra­molecular N—H⋯O(carbon­yl) hydrogen bond. Adjacent mol­ecules are linked by an inter­molecular N—H⋯O(carbon­yl) hydrogen bond, forming a zigzag chain that runs along the c axis.
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spelling pubmed-29690982010-12-30 Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate Jiao, Yuan-Hong Zhang, Qian Meng, Fa-Yan Teng, Lei Yuan, Jia Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The pyranyl ring of the title compound, C(22)H(19)NO(3), adopts a flattened-boat conformation. The dihedral angle between naphthalene and phenyl rings is 78.3 (1)°The mol­ecule also features an intra­molecular N—H⋯O(carbon­yl) hydrogen bond. Adjacent mol­ecules are linked by an inter­molecular N—H⋯O(carbon­yl) hydrogen bond, forming a zigzag chain that runs along the c axis. International Union of Crystallography 2009-03-14 /pmc/articles/PMC2969098/ /pubmed/21582501 http://dx.doi.org/10.1107/S1600536809008885 Text en © Jiao et al. 2009 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
Jiao, Yuan-Hong
Zhang, Qian
Meng, Fa-Yan
Teng, Lei
Yuan, Jia
Ng, Seik Weng
Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title_full Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title_fullStr Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title_full_unstemmed Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title_short Ethyl 3-amino-1-phenyl-1H-benzo[f]chromene-2-carboxyl­ate
title_sort ethyl 3-amino-1-phenyl-1h-benzo[f]chromene-2-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969098/
https://www.ncbi.nlm.nih.gov/pubmed/21582501
http://dx.doi.org/10.1107/S1600536809008885
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AT tenglei ethyl3amino1phenyl1hbenzofchromene2carboxylate
AT yuanjia ethyl3amino1phenyl1hbenzofchromene2carboxylate
AT ngseikweng ethyl3amino1phenyl1hbenzofchromene2carboxylate

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