3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate

The title nitro­phenyl pyridine compound, C(20)H(22)N(2)O(6) was synthesized as a degradation product of the hypertension medication nisoldipine. The dihedral angle between the nitro-substituted phenyl ring and the pyridine ring is 75.5 (4)°. There are a number of C—H⋯O inter­actions between symmetr...

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Detalles Bibliográficos
Autores principales: Chen, Hui, Luo, Jing, Jing, Lin-Lin, Jiang, Ru
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980128/
https://www.ncbi.nlm.nih.gov/pubmed/21580183
http://dx.doi.org/10.1107/S1600536809051988
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author Chen, Hui
Luo, Jing
Jing, Lin-Lin
Jiang, Ru
author_facet Chen, Hui
Luo, Jing
Jing, Lin-Lin
Jiang, Ru
author_sort Chen, Hui
collection PubMed
description The title nitro­phenyl pyridine compound, C(20)H(22)N(2)O(6) was synthesized as a degradation product of the hypertension medication nisoldipine. The dihedral angle between the nitro-substituted phenyl ring and the pyridine ring is 75.5 (4)°. There are a number of C—H⋯O inter­actions between symmetry-related mol­ecules>.
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spelling pubmed-29801282010-12-30 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate Chen, Hui Luo, Jing Jing, Lin-Lin Jiang, Ru Acta Crystallogr Sect E Struct Rep Online Organic Papers The title nitro­phenyl pyridine compound, C(20)H(22)N(2)O(6) was synthesized as a degradation product of the hypertension medication nisoldipine. The dihedral angle between the nitro-substituted phenyl ring and the pyridine ring is 75.5 (4)°. There are a number of C—H⋯O inter­actions between symmetry-related mol­ecules>. International Union of Crystallography 2009-12-09 /pmc/articles/PMC2980128/ /pubmed/21580183 http://dx.doi.org/10.1107/S1600536809051988 Text en © Chen 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
Chen, Hui
Luo, Jing
Jing, Lin-Lin
Jiang, Ru
3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title_full 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title_fullStr 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title_full_unstemmed 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title_short 3-Isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
title_sort 3-isobutyl 5-methyl 2,6-dimethyl-4-(2-nitro­phen­yl)pyridine-3,5-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980128/
https://www.ncbi.nlm.nih.gov/pubmed/21580183
http://dx.doi.org/10.1107/S1600536809051988
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AT luojing 3isobutyl5methyl26dimethyl42nitrophenylpyridine35dicarboxylate
AT jinglinlin 3isobutyl5methyl26dimethyl42nitrophenylpyridine35dicarboxylate
AT jiangru 3isobutyl5methyl26dimethyl42nitrophenylpyridine35dicarboxylate

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