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Pyrimidine-2,4-diamine acetone monosolvate
In the title compound, C(4)H(6)N(4)·C(3)H(6)O, the pyrimidine-2,4-diamine molecule is nearly planar (r.m.s. deviation = 0.005 Å), with the endocyclic angles covering the range 114.36 (10)–126.31 (10)°. In the crystal, N—H⋯N and N—H⋯O hydrogen bonds link the molecules into ribbons along [101], and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569783/ https://www.ncbi.nlm.nih.gov/pubmed/23424529 http://dx.doi.org/10.1107/S1600536813001025 |
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author | Draguta, Sergiu Sandhu, Bhupinder Khrustalev, Victor N. Fonari, Marina S. Timofeeva, Tatiana V. |
author_facet | Draguta, Sergiu Sandhu, Bhupinder Khrustalev, Victor N. Fonari, Marina S. Timofeeva, Tatiana V. |
author_sort | Draguta, Sergiu |
collection | PubMed |
description | In the title compound, C(4)H(6)N(4)·C(3)H(6)O, the pyrimidine-2,4-diamine molecule is nearly planar (r.m.s. deviation = 0.005 Å), with the endocyclic angles covering the range 114.36 (10)–126.31 (10)°. In the crystal, N—H⋯N and N—H⋯O hydrogen bonds link the molecules into ribbons along [101], and weak C—H⋯π interactions consolidate further the crystal packing. |
format | Online Article Text |
id | pubmed-3569783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35697832013-02-19 Pyrimidine-2,4-diamine acetone monosolvate Draguta, Sergiu Sandhu, Bhupinder Khrustalev, Victor N. Fonari, Marina S. Timofeeva, Tatiana V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(4)H(6)N(4)·C(3)H(6)O, the pyrimidine-2,4-diamine molecule is nearly planar (r.m.s. deviation = 0.005 Å), with the endocyclic angles covering the range 114.36 (10)–126.31 (10)°. In the crystal, N—H⋯N and N—H⋯O hydrogen bonds link the molecules into ribbons along [101], and weak C—H⋯π interactions consolidate further the crystal packing. International Union of Crystallography 2013-01-19 /pmc/articles/PMC3569783/ /pubmed/23424529 http://dx.doi.org/10.1107/S1600536813001025 Text en © Draguta et al. 2013 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 Draguta, Sergiu Sandhu, Bhupinder Khrustalev, Victor N. Fonari, Marina S. Timofeeva, Tatiana V. Pyrimidine-2,4-diamine acetone monosolvate |
title | Pyrimidine-2,4-diamine acetone monosolvate |
title_full | Pyrimidine-2,4-diamine acetone monosolvate |
title_fullStr | Pyrimidine-2,4-diamine acetone monosolvate |
title_full_unstemmed | Pyrimidine-2,4-diamine acetone monosolvate |
title_short | Pyrimidine-2,4-diamine acetone monosolvate |
title_sort | pyrimidine-2,4-diamine acetone monosolvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569783/ https://www.ncbi.nlm.nih.gov/pubmed/23424529 http://dx.doi.org/10.1107/S1600536813001025 |
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