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(S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one
In the title compound, C(21)H(17)N(3)O(3), the dihydroquinazoline ring adopts a screw-boat conformation and its stereogenic C atom has an S configuration. The dihedral angle between the mean planes of the two hydroxyphenyl rings is 86.61 (12)°. The amino H atom forms an intramolecular hydrogen b...
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/PMC3414304/ https://www.ncbi.nlm.nih.gov/pubmed/22904837 http://dx.doi.org/10.1107/S1600536812030012 |
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author | Tinguiano, Daniel Sy, Adama Thiam, Ibrahima Elhadj Gaye, Mohamed Retailleau, Pascal |
author_facet | Tinguiano, Daniel Sy, Adama Thiam, Ibrahima Elhadj Gaye, Mohamed Retailleau, Pascal |
author_sort | Tinguiano, Daniel |
collection | PubMed |
description | In the title compound, C(21)H(17)N(3)O(3), the dihydroquinazoline ring adopts a screw-boat conformation and its stereogenic C atom has an S configuration. The dihedral angle between the mean planes of the two hydroxyphenyl rings is 86.61 (12)°. The amino H atom forms an intramolecular hydrogen bond with a phenol O atom, while the hydrazine N atom acts as an acceptor for the H atom of the other phenol group. In the crystal, O—H⋯N and O—H⋯O hydrogen bonds and weak C—H⋯centroid(π-ring) intermolecular interactions are observed, forming chains along [1-10] and [110]. |
format | Online Article Text |
id | pubmed-3414304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34143042012-08-17 (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one Tinguiano, Daniel Sy, Adama Thiam, Ibrahima Elhadj Gaye, Mohamed Retailleau, Pascal Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(17)N(3)O(3), the dihydroquinazoline ring adopts a screw-boat conformation and its stereogenic C atom has an S configuration. The dihedral angle between the mean planes of the two hydroxyphenyl rings is 86.61 (12)°. The amino H atom forms an intramolecular hydrogen bond with a phenol O atom, while the hydrazine N atom acts as an acceptor for the H atom of the other phenol group. In the crystal, O—H⋯N and O—H⋯O hydrogen bonds and weak C—H⋯centroid(π-ring) intermolecular interactions are observed, forming chains along [1-10] and [110]. International Union of Crystallography 2012-07-07 /pmc/articles/PMC3414304/ /pubmed/22904837 http://dx.doi.org/10.1107/S1600536812030012 Text en © Tinguiano 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 Tinguiano, Daniel Sy, Adama Thiam, Ibrahima Elhadj Gaye, Mohamed Retailleau, Pascal (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title | (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title_full | (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title_fullStr | (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title_full_unstemmed | (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title_short | (S,E)-3-[(2-Hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one |
title_sort | (s,e)-3-[(2-hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1h)-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414304/ https://www.ncbi.nlm.nih.gov/pubmed/22904837 http://dx.doi.org/10.1107/S1600536812030012 |
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