4-Methyl-6-phenyl­pyrimidin-2-amine

The title compound, C(11)H(11)N(3), was synthesized as part of our research into functionalized pyrimidines. It crystallizes with two independent mol­ecules in the asymmetric unit that differ only in the twist between the two aromatic rings; the torsion angles between the rings are 29.9 (2) and 45.1...

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Detalles Bibliográficos
Autores principales: Li, Zhen-Jiang, Huang, Jun-E, Meng, A-Lan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960917/
https://www.ncbi.nlm.nih.gov/pubmed/21202148
http://dx.doi.org/10.1107/S1600536808008003
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author Li, Zhen-Jiang
Huang, Jun-E
Meng, A-Lan
author_facet Li, Zhen-Jiang
Huang, Jun-E
Meng, A-Lan
author_sort Li, Zhen-Jiang
collection PubMed
description The title compound, C(11)H(11)N(3), was synthesized as part of our research into functionalized pyrimidines. It crystallizes with two independent mol­ecules in the asymmetric unit that differ only in the twist between the two aromatic rings; the torsion angles between the rings are 29.9 (2) and 45.1 (2)°. The crystal packing is dominated by inter­molecular N—H⋯N hydrogen bonds between independent and equivalent mol­ecules, forming an infinite three-dimensional network.
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spelling pubmed-29609172010-12-30 4-Methyl-6-phenyl­pyrimidin-2-amine Li, Zhen-Jiang Huang, Jun-E Meng, A-Lan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(11)N(3), was synthesized as part of our research into functionalized pyrimidines. It crystallizes with two independent mol­ecules in the asymmetric unit that differ only in the twist between the two aromatic rings; the torsion angles between the rings are 29.9 (2) and 45.1 (2)°. The crystal packing is dominated by inter­molecular N—H⋯N hydrogen bonds between independent and equivalent mol­ecules, forming an infinite three-dimensional network. International Union of Crystallography 2008-03-29 /pmc/articles/PMC2960917/ /pubmed/21202148 http://dx.doi.org/10.1107/S1600536808008003 Text en © Li et al. 2008 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, Zhen-Jiang
Huang, Jun-E
Meng, A-Lan
4-Methyl-6-phenyl­pyrimidin-2-amine
title 4-Methyl-6-phenyl­pyrimidin-2-amine
title_full 4-Methyl-6-phenyl­pyrimidin-2-amine
title_fullStr 4-Methyl-6-phenyl­pyrimidin-2-amine
title_full_unstemmed 4-Methyl-6-phenyl­pyrimidin-2-amine
title_short 4-Methyl-6-phenyl­pyrimidin-2-amine
title_sort 4-methyl-6-phenyl­pyrimidin-2-amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960917/
https://www.ncbi.nlm.nih.gov/pubmed/21202148
http://dx.doi.org/10.1107/S1600536808008003
work_keys_str_mv AT lizhenjiang 4methyl6phenylpyrimidin2amine
AT huangjune 4methyl6phenylpyrimidin2amine
AT mengalan 4methyl6phenylpyrimidin2amine

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