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N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide

The title compound, C(19)H(16)N(2)O(4), is of inter­est as a precursor to biologically active substituted quinolines and related compounds. The dihedral angle between the naphthalene ring system and the benzene ring is 81.9 (1)°. The crystal structure is stabilized by N—H⋯O inter­molecular hydrogen...

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Detalles Bibliográficos
Autores principales: NizamMohideen, M., SubbiahPandi, A., Panneer Selvam, N., Perumal, P. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968788/
https://www.ncbi.nlm.nih.gov/pubmed/21582451
http://dx.doi.org/10.1107/S1600536809007442
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author NizamMohideen, M.
SubbiahPandi, A.
Panneer Selvam, N.
Perumal, P. T.
author_facet NizamMohideen, M.
SubbiahPandi, A.
Panneer Selvam, N.
Perumal, P. T.
author_sort NizamMohideen, M.
collection PubMed
description The title compound, C(19)H(16)N(2)O(4), is of inter­est as a precursor to biologically active substituted quinolines and related compounds. The dihedral angle between the naphthalene ring system and the benzene ring is 81.9 (1)°. The crystal structure is stabilized by N—H⋯O inter­molecular hydrogen bonds, linking the mol­ecules into pairs around a center of symmetry. The crystal structure is further stabilized by inter­molecular O—H⋯O hydrogen bonds, which link the mol­ecules into chains running along a axis. An intra­molecular C—H⋯O short contact is also present.
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spelling pubmed-29687882010-12-30 N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide NizamMohideen, M. SubbiahPandi, A. Panneer Selvam, N. Perumal, P. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(16)N(2)O(4), is of inter­est as a precursor to biologically active substituted quinolines and related compounds. The dihedral angle between the naphthalene ring system and the benzene ring is 81.9 (1)°. The crystal structure is stabilized by N—H⋯O inter­molecular hydrogen bonds, linking the mol­ecules into pairs around a center of symmetry. The crystal structure is further stabilized by inter­molecular O—H⋯O hydrogen bonds, which link the mol­ecules into chains running along a axis. An intra­molecular C—H⋯O short contact is also present. International Union of Crystallography 2009-03-06 /pmc/articles/PMC2968788/ /pubmed/21582451 http://dx.doi.org/10.1107/S1600536809007442 Text en © NizamMohideen 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
NizamMohideen, M.
SubbiahPandi, A.
Panneer Selvam, N.
Perumal, P. T.
N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title_full N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title_fullStr N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title_full_unstemmed N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title_short N-[(2-Hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
title_sort n-[(2-hydr­oxy-1-naphthyl)(3-nitro­phenyl)meth­yl]acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968788/
https://www.ncbi.nlm.nih.gov/pubmed/21582451
http://dx.doi.org/10.1107/S1600536809007442
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