Cargando…
(E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide
In the title compound, C(13)H(13)ClN(4)O, the dihedral angle between the aromatic rings is 33.47 (9)° and an intramolecular N—H⋯N hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, resulting in R (2) (2)(8) loops.
| Autores principales: | , , , |
|---|---|
| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2009
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971773/ https://www.ncbi.nlm.nih.gov/pubmed/21578958 http://dx.doi.org/10.1107/S1600536809050685 |
| _version_ | 1782190665731407872 |
|---|---|
| author | Cong, Yunbo Yang, Huibin Yu, Haibo Li, Bin |
| author_facet | Cong, Yunbo Yang, Huibin Yu, Haibo Li, Bin |
| author_sort | Cong, Yunbo |
| collection | PubMed |
| description | In the title compound, C(13)H(13)ClN(4)O, the dihedral angle between the aromatic rings is 33.47 (9)° and an intramolecular N—H⋯N hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, resulting in R (2) (2)(8) loops. |
| format | Text |
| id | pubmed-2971773 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2009 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29717732010-12-30 (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide Cong, Yunbo Yang, Huibin Yu, Haibo Li, Bin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(13)ClN(4)O, the dihedral angle between the aromatic rings is 33.47 (9)° and an intramolecular N—H⋯N hydrogen bond generates an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, resulting in R (2) (2)(8) loops. International Union of Crystallography 2009-11-28 /pmc/articles/PMC2971773/ /pubmed/21578958 http://dx.doi.org/10.1107/S1600536809050685 Text en © Cong 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 Cong, Yunbo Yang, Huibin Yu, Haibo Li, Bin (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title | (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title_full | (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title_fullStr | (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title_full_unstemmed | (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title_short | (E)-2-[(4-Chloro-1,3-dimethyl-1H-pyrazol-5-yl)methyleneamino]benzamide |
| title_sort | (e)-2-[(4-chloro-1,3-dimethyl-1h-pyrazol-5-yl)methyleneamino]benzamide |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971773/ https://www.ncbi.nlm.nih.gov/pubmed/21578958 http://dx.doi.org/10.1107/S1600536809050685 |
| work_keys_str_mv | AT congyunbo e24chloro13dimethyl1hpyrazol5ylmethyleneaminobenzamide AT yanghuibin e24chloro13dimethyl1hpyrazol5ylmethyleneaminobenzamide AT yuhaibo e24chloro13dimethyl1hpyrazol5ylmethyleneaminobenzamide AT libin e24chloro13dimethyl1hpyrazol5ylmethyleneaminobenzamide |