2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide

In the title compound, C(18)H(16)N(2)O(3), the dihedral angle between the naphthalene ring system and the pyridyl ring is 18.1 (8)°. The mol­ecules are inter­connected via C—H⋯O and O—H⋯O hydrogen bonds. Inversion-related mol­ecules are linked by O—H⋯O hydrogen bonds into cyclic centrosymmetric R (2...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Jebas, Samuel Robinson, Jana, Subrata, Chakrabarty, Rinku, Goswami, Shyamaprasad
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961012/
https://www.ncbi.nlm.nih.gov/pubmed/21202090
http://dx.doi.org/10.1107/S1600536808006211
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author Fun, Hoong-Kun
Jebas, Samuel Robinson
Jana, Subrata
Chakrabarty, Rinku
Goswami, Shyamaprasad
author_facet Fun, Hoong-Kun
Jebas, Samuel Robinson
Jana, Subrata
Chakrabarty, Rinku
Goswami, Shyamaprasad
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(18)H(16)N(2)O(3), the dihedral angle between the naphthalene ring system and the pyridyl ring is 18.1 (8)°. The mol­ecules are inter­connected via C—H⋯O and O—H⋯O hydrogen bonds. Inversion-related mol­ecules are linked by O—H⋯O hydrogen bonds into cyclic centrosymmetric R (2) (2)(22) dimers. Intra­molecular N—H⋯O hydrogen bonding produces an S(5) ring motif. The crystal structure is further stabilized by weak C—H—π inter­actions.
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spelling pubmed-29610122010-12-30 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide Fun, Hoong-Kun Jebas, Samuel Robinson Jana, Subrata Chakrabarty, Rinku Goswami, Shyamaprasad Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(16)N(2)O(3), the dihedral angle between the naphthalene ring system and the pyridyl ring is 18.1 (8)°. The mol­ecules are inter­connected via C—H⋯O and O—H⋯O hydrogen bonds. Inversion-related mol­ecules are linked by O—H⋯O hydrogen bonds into cyclic centrosymmetric R (2) (2)(22) dimers. Intra­molecular N—H⋯O hydrogen bonding produces an S(5) ring motif. The crystal structure is further stabilized by weak C—H—π inter­actions. International Union of Crystallography 2008-03-12 /pmc/articles/PMC2961012/ /pubmed/21202090 http://dx.doi.org/10.1107/S1600536808006211 Text en © Fun 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
Fun, Hoong-Kun
Jebas, Samuel Robinson
Jana, Subrata
Chakrabarty, Rinku
Goswami, Shyamaprasad
2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title_full 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title_fullStr 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title_full_unstemmed 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title_short 2-(7-Hydr­oxy-2-naphth­yloxy)-N-(6-methyl-2-pyrid­yl)acetamide
title_sort 2-(7-hydr­oxy-2-naphth­yloxy)-n-(6-methyl-2-pyrid­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961012/
https://www.ncbi.nlm.nih.gov/pubmed/21202090
http://dx.doi.org/10.1107/S1600536808006211
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