4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione

In the title compound, C(13)H(12)N(4)OS, the dihedral angle between the triazole and naphthalene ring systems is 67.42 (5)°. In the crystal, adjacent mol­ecules are linked via two pairs of inter­molecular N—H⋯S inter­actions, forming R (2) (2)(8) and R (2) (2)(10) ring motifs. Weak C—H⋯S inter­actio...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Vijesh, A. M., Malladi, Shridhar, Isloor, Arun M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980099/
https://www.ncbi.nlm.nih.gov/pubmed/21580136
http://dx.doi.org/10.1107/S1600536809051368
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author Fun, Hoong-Kun
Quah, Ching Kheng
Vijesh, A. M.
Malladi, Shridhar
Isloor, Arun M.
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Vijesh, A. M.
Malladi, Shridhar
Isloor, Arun M.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(13)H(12)N(4)OS, the dihedral angle between the triazole and naphthalene ring systems is 67.42 (5)°. In the crystal, adjacent mol­ecules are linked via two pairs of inter­molecular N—H⋯S inter­actions, forming R (2) (2)(8) and R (2) (2)(10) ring motifs. Weak C—H⋯S inter­actions generate infinite chains along [001] and the structure is further consolidated by C–H⋯π bonds and aromatic π⋯π stacking inter­actions [distance between the centroids of the triazole rings = 3.2479 (7) Å].
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spelling pubmed-29800992010-12-30 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione Fun, Hoong-Kun Quah, Ching Kheng Vijesh, A. M. Malladi, Shridhar Isloor, Arun M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(12)N(4)OS, the dihedral angle between the triazole and naphthalene ring systems is 67.42 (5)°. In the crystal, adjacent mol­ecules are linked via two pairs of inter­molecular N—H⋯S inter­actions, forming R (2) (2)(8) and R (2) (2)(10) ring motifs. Weak C—H⋯S inter­actions generate infinite chains along [001] and the structure is further consolidated by C–H⋯π bonds and aromatic π⋯π stacking inter­actions [distance between the centroids of the triazole rings = 3.2479 (7) Å]. International Union of Crystallography 2009-12-04 /pmc/articles/PMC2980099/ /pubmed/21580136 http://dx.doi.org/10.1107/S1600536809051368 Text en © Fun et al. 2010 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
Quah, Ching Kheng
Vijesh, A. M.
Malladi, Shridhar
Isloor, Arun M.
4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title_full 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title_fullStr 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title_full_unstemmed 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title_short 4-Amino-3-(1-naphthyl­oxymeth­yl)-1H-1,2,4-triazole-5(4H)-thione
title_sort 4-amino-3-(1-naphthyl­oxymeth­yl)-1h-1,2,4-triazole-5(4h)-thione
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980099/
https://www.ncbi.nlm.nih.gov/pubmed/21580136
http://dx.doi.org/10.1107/S1600536809051368
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