tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate

In the crystal structure of the title compound, C(16)H(24)N(4)O(4), mol­ecules are linked by N—H⋯O hydrogen bonds between the carbonyl groups of the carbamoyl and amido functional groups and the amino groups, and by N—H⋯N hydrogen bonds between the amino group and the pyridine ring, forming two-dime...

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Autores principales: Ronga, Luisa, Pinaud, Noel, Rimbault, Charlotte, Marchivie, Mathieu, Guillon, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790400/
https://www.ncbi.nlm.nih.gov/pubmed/24098219
http://dx.doi.org/10.1107/S1600536813024598
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author Ronga, Luisa
Pinaud, Noel
Rimbault, Charlotte
Marchivie, Mathieu
Guillon, Jean
author_facet Ronga, Luisa
Pinaud, Noel
Rimbault, Charlotte
Marchivie, Mathieu
Guillon, Jean
author_sort Ronga, Luisa
collection PubMed
description In the crystal structure of the title compound, C(16)H(24)N(4)O(4), mol­ecules are linked by N—H⋯O hydrogen bonds between the carbonyl groups of the carbamoyl and amido functional groups and the amino groups, and by N—H⋯N hydrogen bonds between the amino group and the pyridine ring, forming two-dimensional networks parallel to the ab plane.
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spelling pubmed-37904002013-10-04 tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate Ronga, Luisa Pinaud, Noel Rimbault, Charlotte Marchivie, Mathieu Guillon, Jean Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(16)H(24)N(4)O(4), mol­ecules are linked by N—H⋯O hydrogen bonds between the carbonyl groups of the carbamoyl and amido functional groups and the amino groups, and by N—H⋯N hydrogen bonds between the amino group and the pyridine ring, forming two-dimensional networks parallel to the ab plane. International Union of Crystallography 2013-09-12 /pmc/articles/PMC3790400/ /pubmed/24098219 http://dx.doi.org/10.1107/S1600536813024598 Text en © Ronga 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
Ronga, Luisa
Pinaud, Noel
Rimbault, Charlotte
Marchivie, Mathieu
Guillon, Jean
tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title_full tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title_fullStr tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title_full_unstemmed tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title_short tert-Butyl N-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
title_sort tert-butyl n-{[5-(5-oxohexa­namido)­pyridin-2-yl]amino}­carbamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790400/
https://www.ncbi.nlm.nih.gov/pubmed/24098219
http://dx.doi.org/10.1107/S1600536813024598
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AT marchiviemathieu tertbutyln55oxohexanamidopyridin2ylaminocarbamate
AT guillonjean tertbutyln55oxohexanamidopyridin2ylaminocarbamate

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