Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate

In the title compound, C(13)H(18)N(2)O(3), the two H atoms of the NH(2) group are engaged in hydrogen bonding with the N atom of the cyano group and with one O atom of the ethoxy­carbonyl group, building a chain parallel to the [100] direction. The N—H⋯N hydrogen bonds assemble the mol­ecules around...

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Autores principales: Messaâd, Mehdi, Hamdi, Besma, Chabchoub, Fakher, Ben Salah, Abdelhamid, Salem, Mansour
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967956/
https://www.ncbi.nlm.nih.gov/pubmed/21581681
http://dx.doi.org/10.1107/S160053680804052X
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author Messaâd, Mehdi
Hamdi, Besma
Chabchoub, Fakher
Ben Salah, Abdelhamid
Salem, Mansour
author_facet Messaâd, Mehdi
Hamdi, Besma
Chabchoub, Fakher
Ben Salah, Abdelhamid
Salem, Mansour
author_sort Messaâd, Mehdi
collection PubMed
description In the title compound, C(13)H(18)N(2)O(3), the two H atoms of the NH(2) group are engaged in hydrogen bonding with the N atom of the cyano group and with one O atom of the ethoxy­carbonyl group, building a chain parallel to the [100] direction. The N—H⋯N hydrogen bonds assemble the mol­ecules around inversion centres, forming dimers with an R (2) (2)(12) graph-set motif.
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spelling pubmed-29679562010-12-30 Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate Messaâd, Mehdi Hamdi, Besma Chabchoub, Fakher Ben Salah, Abdelhamid Salem, Mansour Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(18)N(2)O(3), the two H atoms of the NH(2) group are engaged in hydrogen bonding with the N atom of the cyano group and with one O atom of the ethoxy­carbonyl group, building a chain parallel to the [100] direction. The N—H⋯N hydrogen bonds assemble the mol­ecules around inversion centres, forming dimers with an R (2) (2)(12) graph-set motif. International Union of Crystallography 2008-12-06 /pmc/articles/PMC2967956/ /pubmed/21581681 http://dx.doi.org/10.1107/S160053680804052X Text en © Messaâd et al. 2009 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
Messaâd, Mehdi
Hamdi, Besma
Chabchoub, Fakher
Ben Salah, Abdelhamid
Salem, Mansour
Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title_full Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title_fullStr Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title_full_unstemmed Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title_short Ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4H-pyran-3-carboxyl­ate
title_sort ethyl 6-amino-5-cyano-4-isopropyl-2-methyl-4h-pyran-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967956/
https://www.ncbi.nlm.nih.gov/pubmed/21581681
http://dx.doi.org/10.1107/S160053680804052X
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AT chabchoubfakher ethyl6amino5cyano4isopropyl2methyl4hpyran3carboxylate
AT bensalahabdelhamid ethyl6amino5cyano4isopropyl2methyl4hpyran3carboxylate
AT salemmansour ethyl6amino5cyano4isopropyl2methyl4hpyran3carboxylate

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