tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate

In the crystal of the title compound, C(15)H(23)NO(5)S, mol­ecules are linked through N—H⋯O and O—H⋯O hydrogen-bond inter­actions, resulting in centrosymmetric dimers in which the N—H⋯O inter­actions generate R (2) (2)(12) rings and the O—H⋯O inter­actions generate R (2) (2)(14) rings. Weak inter­mo...

Descripción completa

Detalles Bibliográficos
Autores principales: Fadlalla, Mohamed I., Friedrich, Holger B., Maguire, Glenn E. M., Omondi, Bernard
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052123/
https://www.ncbi.nlm.nih.gov/pubmed/21522400
http://dx.doi.org/10.1107/S1600536811004934
_version_ 1782199632945741824
author Fadlalla, Mohamed I.
Friedrich, Holger B.
Maguire, Glenn E. M.
Omondi, Bernard
author_facet Fadlalla, Mohamed I.
Friedrich, Holger B.
Maguire, Glenn E. M.
Omondi, Bernard
author_sort Fadlalla, Mohamed I.
collection PubMed
description In the crystal of the title compound, C(15)H(23)NO(5)S, mol­ecules are linked through N—H⋯O and O—H⋯O hydrogen-bond inter­actions, resulting in centrosymmetric dimers in which the N—H⋯O inter­actions generate R (2) (2)(12) rings and the O—H⋯O inter­actions generate R (2) (2)(14) rings. Weak inter­molecular C—H⋯O inter­actions are also observed.
format Text
id pubmed-3052123
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30521232011-04-26 tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate Fadlalla, Mohamed I. Friedrich, Holger B. Maguire, Glenn E. M. Omondi, Bernard Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title compound, C(15)H(23)NO(5)S, mol­ecules are linked through N—H⋯O and O—H⋯O hydrogen-bond inter­actions, resulting in centrosymmetric dimers in which the N—H⋯O inter­actions generate R (2) (2)(12) rings and the O—H⋯O inter­actions generate R (2) (2)(14) rings. Weak inter­molecular C—H⋯O inter­actions are also observed. International Union of Crystallography 2011-02-19 /pmc/articles/PMC3052123/ /pubmed/21522400 http://dx.doi.org/10.1107/S1600536811004934 Text en © Fadlalla 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
Fadlalla, Mohamed I.
Friedrich, Holger B.
Maguire, Glenn E. M.
Omondi, Bernard
tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title_full tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title_fullStr tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title_full_unstemmed tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title_short tert-Butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
title_sort tert-butyl 2-hy­droxy-3-(4-methyl­benzene­sulfonamido)­butano­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052123/
https://www.ncbi.nlm.nih.gov/pubmed/21522400
http://dx.doi.org/10.1107/S1600536811004934
work_keys_str_mv AT fadlallamohamedi tertbutyl2hydroxy34methylbenzenesulfonamidobutanoate
AT friedrichholgerb tertbutyl2hydroxy34methylbenzenesulfonamidobutanoate
AT maguireglennem tertbutyl2hydroxy34methylbenzenesulfonamidobutanoate
AT omondibernard tertbutyl2hydroxy34methylbenzenesulfonamidobutanoate

Ejemplares similares