N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine

In the title compound, C(14)H(11)BrN(4), the fused benzene and pyrimidine rings are nearly coplanar, making dihedral angles of 1.26 (14) and 3.53 (15)° in the two independent mol­ecules. In the crystal structure, π–π stacking inter­actions [centroid–centroid distances = 3.4736 (19) and 3.5416 (19) Å...

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Detalles Bibliográficos
Autores principales: Li, De-Liang, Wu, Yang, Wang, Qiang, He, Gu, Yu, Luo-Ting
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979868/
https://www.ncbi.nlm.nih.gov/pubmed/21579862
http://dx.doi.org/10.1107/S1600536810002631
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author Li, De-Liang
Wu, Yang
Wang, Qiang
He, Gu
Yu, Luo-Ting
author_facet Li, De-Liang
Wu, Yang
Wang, Qiang
He, Gu
Yu, Luo-Ting
author_sort Li, De-Liang
collection PubMed
description In the title compound, C(14)H(11)BrN(4), the fused benzene and pyrimidine rings are nearly coplanar, making dihedral angles of 1.26 (14) and 3.53 (15)° in the two independent mol­ecules. In the crystal structure, π–π stacking inter­actions [centroid–centroid distances = 3.4736 (19) and 3.5416 (19) Å] and weak N—H⋯N and N—H⋯Br inter­actions contribute to the stability of the structure.
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spelling pubmed-29798682010-12-30 N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine Li, De-Liang Wu, Yang Wang, Qiang He, Gu Yu, Luo-Ting Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(11)BrN(4), the fused benzene and pyrimidine rings are nearly coplanar, making dihedral angles of 1.26 (14) and 3.53 (15)° in the two independent mol­ecules. In the crystal structure, π–π stacking inter­actions [centroid–centroid distances = 3.4736 (19) and 3.5416 (19) Å] and weak N—H⋯N and N—H⋯Br inter­actions contribute to the stability of the structure. International Union of Crystallography 2010-01-27 /pmc/articles/PMC2979868/ /pubmed/21579862 http://dx.doi.org/10.1107/S1600536810002631 Text en © Li 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
Li, De-Liang
Wu, Yang
Wang, Qiang
He, Gu
Yu, Luo-Ting
N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title_full N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title_fullStr N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title_full_unstemmed N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title_short N (4)-(3-Bromo­phen­yl)quinazoline-4,6-diamine
title_sort n (4)-(3-bromo­phen­yl)quinazoline-4,6-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979868/
https://www.ncbi.nlm.nih.gov/pubmed/21579862
http://dx.doi.org/10.1107/S1600536810002631
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AT yuluoting n43bromophenylquinazoline46diamine

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