Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate

In the title compound, C(18)H(17)NO(5)S, the thia­zine ring adopts a half-chair conformation and the dihedral angle between the aromatic rings is 79.41 (6)°. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions resulting in...

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Autores principales: Arshad, Muhammad Nadeem, Khan, Islam Ullah, Zia-ur-Rehman, Muhammad, Danish, Muhammad, Holman, K. Travis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239077/
https://www.ncbi.nlm.nih.gov/pubmed/22199925
http://dx.doi.org/10.1107/S160053681104966X
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author Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Danish, Muhammad
Holman, K. Travis
author_facet Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Danish, Muhammad
Holman, K. Travis
author_sort Arshad, Muhammad Nadeem
collection PubMed
description In the title compound, C(18)H(17)NO(5)S, the thia­zine ring adopts a half-chair conformation and the dihedral angle between the aromatic rings is 79.41 (6)°. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions resulting in infinite sheets along the b and c axes.
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spelling pubmed-32390772011-12-23 Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate Arshad, Muhammad Nadeem Khan, Islam Ullah Zia-ur-Rehman, Muhammad Danish, Muhammad Holman, K. Travis Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(17)NO(5)S, the thia­zine ring adopts a half-chair conformation and the dihedral angle between the aromatic rings is 79.41 (6)°. An intra­molecular O—H⋯O hydrogen bond generates an S(6) ring. In the crystal, mol­ecules are linked by weak C—H⋯O inter­actions resulting in infinite sheets along the b and c axes. International Union of Crystallography 2011-11-25 /pmc/articles/PMC3239077/ /pubmed/22199925 http://dx.doi.org/10.1107/S160053681104966X Text en © Arshad et al. 2011 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
Arshad, Muhammad Nadeem
Khan, Islam Ullah
Zia-ur-Rehman, Muhammad
Danish, Muhammad
Holman, K. Travis
Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title_full Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title_fullStr Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title_full_unstemmed Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title_short Methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2H-1λ(6),2-benzothia­zine-3-carboxyl­ate
title_sort methyl 4-hy­droxy-1,1-dioxo-2-(2-phenyl­eth­yl)-2h-1λ(6),2-benzothia­zine-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239077/
https://www.ncbi.nlm.nih.gov/pubmed/22199925
http://dx.doi.org/10.1107/S160053681104966X
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