Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide

The title compounds, C(19)H(12)Br(2)N(2)O(2) and C(18)H(11)Br(2)N(3)O(2), were synthesized in good yields from condensation reactions of 3-bromo­benzoyl chloride with 2-amino­pyridine or 2-amino­pyrimidine using standard condensation reaction conditions and subsequent column chromatography.

Detalles Bibliográficos
Autores principales: Desmond, Féilim, Gallagher, John F., Hehir, Niall
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Research Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784653/
https://www.ncbi.nlm.nih.gov/pubmed/33520256
http://dx.doi.org/10.1107/S2056989020014413
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author Desmond, Féilim
Gallagher, John F.
Hehir, Niall
author_facet Desmond, Féilim
Gallagher, John F.
Hehir, Niall
author_sort Desmond, Féilim
collection PubMed
description The title compounds, C(19)H(12)Br(2)N(2)O(2) and C(18)H(11)Br(2)N(3)O(2), were synthesized in good yields from condensation reactions of 3-bromo­benzoyl chloride with 2-amino­pyridine or 2-amino­pyrimidine using standard condensation reaction conditions and subsequent column chromatography.
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spelling pubmed-77846532021-01-29 Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide Desmond, Féilim Gallagher, John F. Hehir, Niall Acta Crystallogr E Crystallogr Commun Research Communications The title compounds, C(19)H(12)Br(2)N(2)O(2) and C(18)H(11)Br(2)N(3)O(2), were synthesized in good yields from condensation reactions of 3-bromo­benzoyl chloride with 2-amino­pyridine or 2-amino­pyrimidine using standard condensation reaction conditions and subsequent column chromatography. International Union of Crystallography 2020-11-03 /pmc/articles/PMC7784653/ /pubmed/33520256 http://dx.doi.org/10.1107/S2056989020014413 Text en © Desmond et al. 2020 http://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.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Communications
Desmond, Féilim
Gallagher, John F.
Hehir, Niall
Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title_full Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title_fullStr Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title_full_unstemmed Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title_short Two acyclic imides: 3-bromo-N-(3-bromo­benzo­yl)-N-(pyridin-2-yl)benzamide and 3-bromo-N-(3-bromo­benzo­yl)-N-(pyrimidin-2-yl)benzamide
title_sort two acyclic imides: 3-bromo-n-(3-bromo­benzo­yl)-n-(pyridin-2-yl)benzamide and 3-bromo-n-(3-bromo­benzo­yl)-n-(pyrimidin-2-yl)benzamide
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784653/
https://www.ncbi.nlm.nih.gov/pubmed/33520256
http://dx.doi.org/10.1107/S2056989020014413
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AT gallagherjohnf twoacyclicimides3bromon3bromobenzoylnpyridin2ylbenzamideand3bromon3bromobenzoylnpyrimidin2ylbenzamide
AT hehirniall twoacyclicimides3bromon3bromobenzoylnpyridin2ylbenzamideand3bromon3bromobenzoylnpyrimidin2ylbenzamide

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