3-Amino-5-bromo-2-iodo­pyridine

The reaction of 3-amino-5-bromo­pyridine with N-iodo­succinimide in the presence of acetic acid produces the title compound, C(5)H(4)BrIN, with an iodo substituent in position 2 of the pyridine ring. The crystal structure features rather weak inter­molecular N—H⋯N hydrogen bonds linking the mol­ecul...

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Detalles Bibliográficos
Autores principales: Bunker, Kevin D., Sach, Neal W., Nukui, Seiji, Rheingold, Arnold L., Yanovsky, Alex
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967947/
https://www.ncbi.nlm.nih.gov/pubmed/21581671
http://dx.doi.org/10.1107/S1600536808040452
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author Bunker, Kevin D.
Sach, Neal W.
Nukui, Seiji
Rheingold, Arnold L.
Yanovsky, Alex
author_facet Bunker, Kevin D.
Sach, Neal W.
Nukui, Seiji
Rheingold, Arnold L.
Yanovsky, Alex
author_sort Bunker, Kevin D.
collection PubMed
description The reaction of 3-amino-5-bromo­pyridine with N-iodo­succinimide in the presence of acetic acid produces the title compound, C(5)H(4)BrIN, with an iodo substituent in position 2 of the pyridine ring. The crystal structure features rather weak inter­molecular N—H⋯N hydrogen bonds linking the mol­ecules into chains along the z axis of the crystal.
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spelling pubmed-29679472010-12-30 3-Amino-5-bromo-2-iodo­pyridine Bunker, Kevin D. Sach, Neal W. Nukui, Seiji Rheingold, Arnold L. Yanovsky, Alex Acta Crystallogr Sect E Struct Rep Online Organic Papers The reaction of 3-amino-5-bromo­pyridine with N-iodo­succinimide in the presence of acetic acid produces the title compound, C(5)H(4)BrIN, with an iodo substituent in position 2 of the pyridine ring. The crystal structure features rather weak inter­molecular N—H⋯N hydrogen bonds linking the mol­ecules into chains along the z axis of the crystal. International Union of Crystallography 2008-12-06 /pmc/articles/PMC2967947/ /pubmed/21581671 http://dx.doi.org/10.1107/S1600536808040452 Text en © Bunker et al. 2009 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
Bunker, Kevin D.
Sach, Neal W.
Nukui, Seiji
Rheingold, Arnold L.
Yanovsky, Alex
3-Amino-5-bromo-2-iodo­pyridine
title 3-Amino-5-bromo-2-iodo­pyridine
title_full 3-Amino-5-bromo-2-iodo­pyridine
title_fullStr 3-Amino-5-bromo-2-iodo­pyridine
title_full_unstemmed 3-Amino-5-bromo-2-iodo­pyridine
title_short 3-Amino-5-bromo-2-iodo­pyridine
title_sort 3-amino-5-bromo-2-iodo­pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967947/
https://www.ncbi.nlm.nih.gov/pubmed/21581671
http://dx.doi.org/10.1107/S1600536808040452
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AT sachnealw 3amino5bromo2iodopyridine
AT nukuiseiji 3amino5bromo2iodopyridine
AT rheingoldarnoldl 3amino5bromo2iodopyridine
AT yanovskyalex 3amino5bromo2iodopyridine

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