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Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine

In the structure of the title compound, C(15)H(19)N(3)O(5)S(2), the bond lengths at the linking sulfur atom are significantly different [1.7473 (17) and 1.811 (2) Å], and the angle at the exocyclic nitro­gen atom is wide at 128.45 (18)°. The inter­planar angle between the tolyl and thia­diazole ring...

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Autores principales: Abu-Zaied, Mamdouh A., Hebishy, Ali M. S., Elgemeie, Galal H., Salama, Hagar T., Jones, Peter G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439424/
https://www.ncbi.nlm.nih.gov/pubmed/37601574
http://dx.doi.org/10.1107/S2056989023005248
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author Abu-Zaied, Mamdouh A.
Hebishy, Ali M. S.
Elgemeie, Galal H.
Salama, Hagar T.
Jones, Peter G.
author_facet Abu-Zaied, Mamdouh A.
Hebishy, Ali M. S.
Elgemeie, Galal H.
Salama, Hagar T.
Jones, Peter G.
author_sort Abu-Zaied, Mamdouh A.
collection PubMed
description In the structure of the title compound, C(15)H(19)N(3)O(5)S(2), the bond lengths at the linking sulfur atom are significantly different [1.7473 (17) and 1.811 (2) Å], and the angle at the exocyclic nitro­gen atom is wide at 128.45 (18)°. The inter­planar angle between the tolyl and thia­diazole rings is 9.2 (1)°. The complex hydrogen-bonding pattern, involving five donors and five acceptors, can be broken down into a one-dimensional ribbon parallel to the b axis, involving hydrogen bonds of the sugar residues only, and a two-dimensional layer structure parallel to the ab plane, based on the N—H⋯O and O—H⋯N hydrogen bonds.
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spelling pubmed-104394242023-08-20 Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine Abu-Zaied, Mamdouh A. Hebishy, Ali M. S. Elgemeie, Galal H. Salama, Hagar T. Jones, Peter G. Acta Crystallogr E Crystallogr Commun Research Communications In the structure of the title compound, C(15)H(19)N(3)O(5)S(2), the bond lengths at the linking sulfur atom are significantly different [1.7473 (17) and 1.811 (2) Å], and the angle at the exocyclic nitro­gen atom is wide at 128.45 (18)°. The inter­planar angle between the tolyl and thia­diazole rings is 9.2 (1)°. The complex hydrogen-bonding pattern, involving five donors and five acceptors, can be broken down into a one-dimensional ribbon parallel to the b axis, involving hydrogen bonds of the sugar residues only, and a two-dimensional layer structure parallel to the ab plane, based on the N—H⋯O and O—H⋯N hydrogen bonds. International Union of Crystallography 2023-06-20 /pmc/articles/PMC10439424/ /pubmed/37601574 http://dx.doi.org/10.1107/S2056989023005248 Text en © Abu-Zaied et al. 2023 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Communications
Abu-Zaied, Mamdouh A.
Hebishy, Ali M. S.
Elgemeie, Galal H.
Salama, Hagar T.
Jones, Peter G.
Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title_full Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title_fullStr Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title_full_unstemmed Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title_short Crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-N-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
title_sort crystal structure of 5-(β-d-gluco­pyran­osyl­thio)-n-(4-methyl­phen­yl)-1,3,4-thia­diazol-2-amine
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439424/
https://www.ncbi.nlm.nih.gov/pubmed/37601574
http://dx.doi.org/10.1107/S2056989023005248
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