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3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one

In the title mol­ecule, C(19)H(14)ClN(3)O, the quinoline and quinazoline ring systems form a dihedral angle of 80.75 (4)°. In the crystal, the mol­ecules are linked by pairs of C—H⋯N hydrogen bonds into centrosymmetric dimers, generating R (2) (2)(6) ring motifs. The structure is further stabilized...

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Detalles Bibliográficos
Autores principales: Roopan, S. Mohana, Khan, F. Nawaz, Kone, Sriramakrishnaswamy, Hathwar, Venkatesha R., Akkurt, Mehmet
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006817/
https://www.ncbi.nlm.nih.gov/pubmed/21587791
http://dx.doi.org/10.1107/S1600536810020830
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author Roopan, S. Mohana
Khan, F. Nawaz
Kone, Sriramakrishnaswamy
Hathwar, Venkatesha R.
Akkurt, Mehmet
author_facet Roopan, S. Mohana
Khan, F. Nawaz
Kone, Sriramakrishnaswamy
Hathwar, Venkatesha R.
Akkurt, Mehmet
author_sort Roopan, S. Mohana
collection PubMed
description In the title mol­ecule, C(19)H(14)ClN(3)O, the quinoline and quinazoline ring systems form a dihedral angle of 80.75 (4)°. In the crystal, the mol­ecules are linked by pairs of C—H⋯N hydrogen bonds into centrosymmetric dimers, generating R (2) (2)(6) ring motifs. The structure is further stabilized by C—H⋯π inter­actions and π–π stacking inter­actions [centroid–centroid distances = 3.7869 (8) and 3.8490 (8) Å].
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spelling pubmed-30068172010-12-30 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one Roopan, S. Mohana Khan, F. Nawaz Kone, Sriramakrishnaswamy Hathwar, Venkatesha R. Akkurt, Mehmet Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(19)H(14)ClN(3)O, the quinoline and quinazoline ring systems form a dihedral angle of 80.75 (4)°. In the crystal, the mol­ecules are linked by pairs of C—H⋯N hydrogen bonds into centrosymmetric dimers, generating R (2) (2)(6) ring motifs. The structure is further stabilized by C—H⋯π inter­actions and π–π stacking inter­actions [centroid–centroid distances = 3.7869 (8) and 3.8490 (8) Å]. International Union of Crystallography 2010-06-05 /pmc/articles/PMC3006817/ /pubmed/21587791 http://dx.doi.org/10.1107/S1600536810020830 Text en © Roopan 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
Roopan, S. Mohana
Khan, F. Nawaz
Kone, Sriramakrishnaswamy
Hathwar, Venkatesha R.
Akkurt, Mehmet
3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title_full 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title_fullStr 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title_full_unstemmed 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title_short 3-[(2-Chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3H)-one
title_sort 3-[(2-chloro-6-methyl­quinolin-3-yl)meth­yl]quinazolin-4(3h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006817/
https://www.ncbi.nlm.nih.gov/pubmed/21587791
http://dx.doi.org/10.1107/S1600536810020830
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