2-Amino-5-bromo­pyridinium hydrogen succinate

In the title compound, C(5)H(6)BrN(2) (+)·C(4)H(5)O(4) (−), the pyridine N atom of the 2-amino-5-bromo­pyridine mol­ecule is protonated. The protonated N atom and the amino group are linked via N—H⋯O hydrogen bonds to the carboxyl­ate O atoms of the singly deprotonated succinate anion. The hydrogen...

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Detalles Bibliográficos
Autores principales: Hemamalini, Madhukar, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983627/
https://www.ncbi.nlm.nih.gov/pubmed/21580432
http://dx.doi.org/10.1107/S1600536810006495
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author Hemamalini, Madhukar
Fun, Hoong-Kun
author_facet Hemamalini, Madhukar
Fun, Hoong-Kun
author_sort Hemamalini, Madhukar
collection PubMed
description In the title compound, C(5)H(6)BrN(2) (+)·C(4)H(5)O(4) (−), the pyridine N atom of the 2-amino-5-bromo­pyridine mol­ecule is protonated. The protonated N atom and the amino group are linked via N—H⋯O hydrogen bonds to the carboxyl­ate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H⋯O hydrogen bonds. A weak inter­molecular C—H⋯O hydrogen bond is also observed.
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spelling pubmed-29836272010-12-30 2-Amino-5-bromo­pyridinium hydrogen succinate Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(5)H(6)BrN(2) (+)·C(4)H(5)O(4) (−), the pyridine N atom of the 2-amino-5-bromo­pyridine mol­ecule is protonated. The protonated N atom and the amino group are linked via N—H⋯O hydrogen bonds to the carboxyl­ate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H⋯O hydrogen bonds. A weak inter­molecular C—H⋯O hydrogen bond is also observed. International Union of Crystallography 2010-02-27 /pmc/articles/PMC2983627/ /pubmed/21580432 http://dx.doi.org/10.1107/S1600536810006495 Text en © Hemamalini and Fun 2010 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
Hemamalini, Madhukar
Fun, Hoong-Kun
2-Amino-5-bromo­pyridinium hydrogen succinate
title 2-Amino-5-bromo­pyridinium hydrogen succinate
title_full 2-Amino-5-bromo­pyridinium hydrogen succinate
title_fullStr 2-Amino-5-bromo­pyridinium hydrogen succinate
title_full_unstemmed 2-Amino-5-bromo­pyridinium hydrogen succinate
title_short 2-Amino-5-bromo­pyridinium hydrogen succinate
title_sort 2-amino-5-bromo­pyridinium hydrogen succinate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983627/
https://www.ncbi.nlm.nih.gov/pubmed/21580432
http://dx.doi.org/10.1107/S1600536810006495
work_keys_str_mv AT hemamalinimadhukar 2amino5bromopyridiniumhydrogensuccinate
AT funhoongkun 2amino5bromopyridiniumhydrogensuccinate

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