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Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate

In the title compound, C(20)H(29)N(5)O(4), the pyridine ring makes a dihedral angle of 10.41 (16)° with the triazole ring, which exhibits an azo-like character. In the crystal, mol­ecules are linked by C—H⋯O and C—H⋯N hydrogen bonds, and C—H⋯π inter­actions involving a methyl group and the pyridine...

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Detalles Bibliográficos
Autores principales: François, Alison, Marty, Louise, Picard, Claude, Mallet-Ladeira, Sonia, Benoist, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515257/
https://www.ncbi.nlm.nih.gov/pubmed/23284477
http://dx.doi.org/10.1107/S1600536812042596
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author François, Alison
Marty, Louise
Picard, Claude
Mallet-Ladeira, Sonia
Benoist, Eric
author_facet François, Alison
Marty, Louise
Picard, Claude
Mallet-Ladeira, Sonia
Benoist, Eric
author_sort François, Alison
collection PubMed
description In the title compound, C(20)H(29)N(5)O(4), the pyridine ring makes a dihedral angle of 10.41 (16)° with the triazole ring, which exhibits an azo-like character. In the crystal, mol­ecules are linked by C—H⋯O and C—H⋯N hydrogen bonds, and C—H⋯π inter­actions involving a methyl group and the pyridine ring of a neighbouring mol­ecule, leading to the formation of a three-dimensional network.
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spelling pubmed-35152572013-01-02 Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate François, Alison Marty, Louise Picard, Claude Mallet-Ladeira, Sonia Benoist, Eric Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(29)N(5)O(4), the pyridine ring makes a dihedral angle of 10.41 (16)° with the triazole ring, which exhibits an azo-like character. In the crystal, mol­ecules are linked by C—H⋯O and C—H⋯N hydrogen bonds, and C—H⋯π inter­actions involving a methyl group and the pyridine ring of a neighbouring mol­ecule, leading to the formation of a three-dimensional network. International Union of Crystallography 2012-10-20 /pmc/articles/PMC3515257/ /pubmed/23284477 http://dx.doi.org/10.1107/S1600536812042596 Text en © François et al. 2012 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
François, Alison
Marty, Louise
Picard, Claude
Mallet-Ladeira, Sonia
Benoist, Eric
Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title_full Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title_fullStr Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title_full_unstemmed Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title_short Di-tert-butyl N-{[1-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl]methyl}iminodiacetate
title_sort di-tert-butyl n-{[1-(pyridin-4-yl)-1h-1,2,3-triazol-4-yl]methyl}iminodiacetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515257/
https://www.ncbi.nlm.nih.gov/pubmed/23284477
http://dx.doi.org/10.1107/S1600536812042596
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