6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one

The title compound, C(7)H(6)BrN(3)O, was obtained from the reaction of 6-bromo-1H-imidazo[4,5-b]pyridin-2(3H)-one with methyl iodide. All non-H atoms lie in a common plane [r.m.s deviation = 0.017 (1) Å]. The amino group is a hydrogen-bond donor to the carbonyl group of an inversion-related mol­ecul...

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Detalles Bibliográficos
Autores principales: Ghacham, Hend Bel, Rodi, Youssef Kandri, Capet, Frédéric, Essassi, El Mokhtar, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979211/
https://www.ncbi.nlm.nih.gov/pubmed/21579134
http://dx.doi.org/10.1107/S1600536810012791
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author Ghacham, Hend Bel
Rodi, Youssef Kandri
Capet, Frédéric
Essassi, El Mokhtar
Ng, Seik Weng
author_facet Ghacham, Hend Bel
Rodi, Youssef Kandri
Capet, Frédéric
Essassi, El Mokhtar
Ng, Seik Weng
author_sort Ghacham, Hend Bel
collection PubMed
description The title compound, C(7)H(6)BrN(3)O, was obtained from the reaction of 6-bromo-1H-imidazo[4,5-b]pyridin-2(3H)-one with methyl iodide. All non-H atoms lie in a common plane [r.m.s deviation = 0.017 (1) Å]. The amino group is a hydrogen-bond donor to the carbonyl group of an inversion-related mol­ecule, the pair of hydrogen bonds giving rise to a hydrogen-bonded dimer.
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spelling pubmed-29792112010-12-30 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one Ghacham, Hend Bel Rodi, Youssef Kandri Capet, Frédéric Essassi, El Mokhtar Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(7)H(6)BrN(3)O, was obtained from the reaction of 6-bromo-1H-imidazo[4,5-b]pyridin-2(3H)-one with methyl iodide. All non-H atoms lie in a common plane [r.m.s deviation = 0.017 (1) Å]. The amino group is a hydrogen-bond donor to the carbonyl group of an inversion-related mol­ecule, the pair of hydrogen bonds giving rise to a hydrogen-bonded dimer. International Union of Crystallography 2010-04-14 /pmc/articles/PMC2979211/ /pubmed/21579134 http://dx.doi.org/10.1107/S1600536810012791 Text en © Ghacham et al. 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
Ghacham, Hend Bel
Rodi, Youssef Kandri
Capet, Frédéric
Essassi, El Mokhtar
Ng, Seik Weng
6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title_full 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title_fullStr 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title_full_unstemmed 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title_short 6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one
title_sort 6-bromo-3-methyl-1h-imidazo[4,5-b]pyridin-2(3h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979211/
https://www.ncbi.nlm.nih.gov/pubmed/21579134
http://dx.doi.org/10.1107/S1600536810012791
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