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(E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate
The title compound, C(20)H(17)N(3)O(2)·CH(4)O·H(2)O, was synthesized by the condensation reaction of 2-benzyloxybenzaldehyde with isoniazid (isonicotinic acid hydrazide). The tricyclic compound displays a trans configuration with respect to the C=N double bond. The central benzene ring makes dihedr...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979361/ https://www.ncbi.nlm.nih.gov/pubmed/21579427 http://dx.doi.org/10.1107/S1600536810016958 |
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author | Naveenkumar, H. S. Sadikun, Amirin Ibrahim, Pazilah Hemamalini, Madhukar Fun, Hoong-Kun |
author_facet | Naveenkumar, H. S. Sadikun, Amirin Ibrahim, Pazilah Hemamalini, Madhukar Fun, Hoong-Kun |
author_sort | Naveenkumar, H. S. |
collection | PubMed |
description | The title compound, C(20)H(17)N(3)O(2)·CH(4)O·H(2)O, was synthesized by the condensation reaction of 2-benzyloxybenzaldehyde with isoniazid (isonicotinic acid hydrazide). The tricyclic compound displays a trans configuration with respect to the C=N double bond. The central benzene ring makes dihedral angles of 8.83 (7) and 70.39 (8)° with the pyridine ring and the terminal benzene ring, respectively. The dihedral angle between the pyridine ring and the terminal benzene ring is 73.11 (8)°. In the crystal structure, molecules are connected by intermolecular N—H⋯O, O—H⋯O, O—H⋯(N,N) and C—H⋯O hydrogen bonds, forming a two-dimensional network perpendicular to the a axis. |
format | Text |
id | pubmed-2979361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29793612010-12-30 (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate Naveenkumar, H. S. Sadikun, Amirin Ibrahim, Pazilah Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(17)N(3)O(2)·CH(4)O·H(2)O, was synthesized by the condensation reaction of 2-benzyloxybenzaldehyde with isoniazid (isonicotinic acid hydrazide). The tricyclic compound displays a trans configuration with respect to the C=N double bond. The central benzene ring makes dihedral angles of 8.83 (7) and 70.39 (8)° with the pyridine ring and the terminal benzene ring, respectively. The dihedral angle between the pyridine ring and the terminal benzene ring is 73.11 (8)°. In the crystal structure, molecules are connected by intermolecular N—H⋯O, O—H⋯O, O—H⋯(N,N) and C—H⋯O hydrogen bonds, forming a two-dimensional network perpendicular to the a axis. International Union of Crystallography 2010-05-15 /pmc/articles/PMC2979361/ /pubmed/21579427 http://dx.doi.org/10.1107/S1600536810016958 Text en © Naveenkumar 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 Naveenkumar, H. S. Sadikun, Amirin Ibrahim, Pazilah Hemamalini, Madhukar Fun, Hoong-Kun (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title | (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title_full | (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title_fullStr | (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title_full_unstemmed | (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title_short | (E)-N′-(2-Benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
title_sort | (e)-n′-(2-benzyloxybenzylidene)isonicotinohydrazide methanol solvate monohydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979361/ https://www.ncbi.nlm.nih.gov/pubmed/21579427 http://dx.doi.org/10.1107/S1600536810016958 |
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