Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate

There are two independent mol­ecules in the asymmetric unit of the title compound, C(19)H(16)N(2)O(5)S, in which the thia­zole rings make dihedral angles of 80.89 (11) and 84.81 (11)° with the pyrano[3,2-c]chromene ring systems. An intra­molecular N—H⋯O hydrogen bond involving the amino group occurs...

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Detalles Bibliográficos
Autores principales: Karthikeyan, V., Ramkumar, V., Karunakaran, R. Joel
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/PMC3884413/
https://www.ncbi.nlm.nih.gov/pubmed/24427048
http://dx.doi.org/10.1107/S1600536813021703
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author Karthikeyan, V.
Ramkumar, V.
Karunakaran, R. Joel
author_facet Karthikeyan, V.
Ramkumar, V.
Karunakaran, R. Joel
author_sort Karthikeyan, V.
collection PubMed
description There are two independent mol­ecules in the asymmetric unit of the title compound, C(19)H(16)N(2)O(5)S, in which the thia­zole rings make dihedral angles of 80.89 (11) and 84.81 (11)° with the pyrano[3,2-c]chromene ring systems. An intra­molecular N—H⋯O hydrogen bond involving the amino group occurs in each independent mol­ecule. In the crystal, the amino groups are involved in N—H⋯O and N—H⋯N hydrogen bonds.
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spelling pubmed-38844132014-01-14 Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate Karthikeyan, V. Ramkumar, V. Karunakaran, R. Joel Acta Crystallogr Sect E Struct Rep Online Organic Papers There are two independent mol­ecules in the asymmetric unit of the title compound, C(19)H(16)N(2)O(5)S, in which the thia­zole rings make dihedral angles of 80.89 (11) and 84.81 (11)° with the pyrano[3,2-c]chromene ring systems. An intra­molecular N—H⋯O hydrogen bond involving the amino group occurs in each independent mol­ecule. In the crystal, the amino groups are involved in N—H⋯O and N—H⋯N hydrogen bonds. International Union of Crystallography 2013-08-10 /pmc/articles/PMC3884413/ /pubmed/24427048 http://dx.doi.org/10.1107/S1600536813021703 Text en © Karthikeyan 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
Karthikeyan, V.
Ramkumar, V.
Karunakaran, R. Joel
Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title_full Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title_fullStr Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title_full_unstemmed Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title_short Ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carboxyl­ate
title_sort ethyl 2-amino-4-(4-methyl-1,3-thia­zol-5-yl)-5-oxo-4h,5h-pyrano[3,2-c]chromene-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884413/
https://www.ncbi.nlm.nih.gov/pubmed/24427048
http://dx.doi.org/10.1107/S1600536813021703
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AT ramkumarv ethyl2amino44methyl13thiazol5yl5oxo4h5hpyrano32cchromene3carboxylate
AT karunakaranrjoel ethyl2amino44methyl13thiazol5yl5oxo4h5hpyrano32cchromene3carboxylate

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