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7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate
The asymmetric unit of the title compound, C(14)H(18)N(3)O(+)·Cl(−)·H(2)O, comprises a substituted amido–naphthyridine cation, a chloride anion and a water molecule of crystallization. Intramolecular C—H⋯O hydrogen bonds generate six-membered rings, producing an S(6) ring motif. The amido group is...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968242/ https://www.ncbi.nlm.nih.gov/pubmed/21581941 http://dx.doi.org/10.1107/S1600536808042955 |
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author | Fun, Hoong-Kun Kia, Reza Das, Nirmal Kumar Sen, Debabrata Goswami, Shyamaprosad |
author_facet | Fun, Hoong-Kun Kia, Reza Das, Nirmal Kumar Sen, Debabrata Goswami, Shyamaprosad |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | The asymmetric unit of the title compound, C(14)H(18)N(3)O(+)·Cl(−)·H(2)O, comprises a substituted amido–naphthyridine cation, a chloride anion and a water molecule of crystallization. Intramolecular C—H⋯O hydrogen bonds generate six-membered rings, producing an S(6) ring motif. The amido group is twisted from the naphthyridine ring, making a dihedral angle of 17.65 (7)°. The crystal structure is stabilized by intermolecular N—H⋯O, N—H⋯Cl, O—H⋯Cl (× 2), and C—H⋯O (× 2) hydrogen bonds. These interactions linked neighbouring molecules into chains along the a and b axes of the crystal, thus forming molecular sheets parallel to the (001) plane. |
format | Text |
id | pubmed-2968242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29682422010-12-30 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate Fun, Hoong-Kun Kia, Reza Das, Nirmal Kumar Sen, Debabrata Goswami, Shyamaprosad Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(14)H(18)N(3)O(+)·Cl(−)·H(2)O, comprises a substituted amido–naphthyridine cation, a chloride anion and a water molecule of crystallization. Intramolecular C—H⋯O hydrogen bonds generate six-membered rings, producing an S(6) ring motif. The amido group is twisted from the naphthyridine ring, making a dihedral angle of 17.65 (7)°. The crystal structure is stabilized by intermolecular N—H⋯O, N—H⋯Cl, O—H⋯Cl (× 2), and C—H⋯O (× 2) hydrogen bonds. These interactions linked neighbouring molecules into chains along the a and b axes of the crystal, thus forming molecular sheets parallel to the (001) plane. International Union of Crystallography 2009-01-17 /pmc/articles/PMC2968242/ /pubmed/21581941 http://dx.doi.org/10.1107/S1600536808042955 Text en © Fun 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 Fun, Hoong-Kun Kia, Reza Das, Nirmal Kumar Sen, Debabrata Goswami, Shyamaprosad 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title | 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title_full | 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title_fullStr | 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title_full_unstemmed | 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title_short | 7-(2,2-Dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
title_sort | 7-(2,2-dimethylpropanamido)-2-methyl-1,8-naphthyridin-1-ium chloride monohydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968242/ https://www.ncbi.nlm.nih.gov/pubmed/21581941 http://dx.doi.org/10.1107/S1600536808042955 |
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