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2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide
In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thiazole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414920/ https://www.ncbi.nlm.nih.gov/pubmed/22904907 http://dx.doi.org/10.1107/S1600536812031583 |
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author | Fun, Hoong-Kun Quah, Ching Kheng Nayak, Prakash S. Narayana, B. Sarojini, B. K. |
author_facet | Fun, Hoong-Kun Quah, Ching Kheng Nayak, Prakash S. Narayana, B. Sarojini, B. K. |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thiazole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The dimers are linked by C—H⋯O hydrogen bonds into chains propagating along [110]. |
format | Online Article Text |
id | pubmed-3414920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34149202012-08-17 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide Fun, Hoong-Kun Quah, Ching Kheng Nayak, Prakash S. Narayana, B. Sarojini, B. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(12)N(2)OS, the naphthalene ring system [maximum deviation = 0.026 (1) Å] forms a dihedral angle of 85.69 (6)° with the thiazole ring [maximum deviation = 0.010 (1) Å]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R (2) (2)(8) loops. The dimers are linked by C—H⋯O hydrogen bonds into chains propagating along [110]. International Union of Crystallography 2012-07-18 /pmc/articles/PMC3414920/ /pubmed/22904907 http://dx.doi.org/10.1107/S1600536812031583 Text en © Fun et al. 2012 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 Nayak, Prakash S. Narayana, B. Sarojini, B. K. 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title | 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title_full | 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title_fullStr | 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title_full_unstemmed | 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title_short | 2-(Naphthalen-1-yl)-N-(1,3-thiazol-2-yl)acetamide |
title_sort | 2-(naphthalen-1-yl)-n-(1,3-thiazol-2-yl)acetamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414920/ https://www.ncbi.nlm.nih.gov/pubmed/22904907 http://dx.doi.org/10.1107/S1600536812031583 |
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