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2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide

In the title compound, C(18)H(21)BrN(2)O(5), conjugation between the π-donating N—C—O fragment and the π-withdrawing carbonyl group results in considerable redistribution of the electron density within the dihydropyridinol ring. This effect is also promoted by the formation of an intra­molecular N—H...

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Autores principales: Shishkina, Svetlana V., Shishkin, Oleg V., Ukrainets, Igor V., Bereznyakova, Nataliya L., Davidenko, Alexandra A.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961529/
https://www.ncbi.nlm.nih.gov/pubmed/21202555
http://dx.doi.org/10.1107/S1600536808013378
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author Shishkina, Svetlana V.
Shishkin, Oleg V.
Ukrainets, Igor V.
Bereznyakova, Nataliya L.
Davidenko, Alexandra A.
author_facet Shishkina, Svetlana V.
Shishkin, Oleg V.
Ukrainets, Igor V.
Bereznyakova, Nataliya L.
Davidenko, Alexandra A.
author_sort Shishkina, Svetlana V.
collection PubMed
description In the title compound, C(18)H(21)BrN(2)O(5), conjugation between the π-donating N—C—O fragment and the π-withdrawing carbonyl group results in considerable redistribution of the electron density within the dihydropyridinol ring. This effect is also promoted by the formation of an intra­molecular N—H⋯O hydrogen bond. The five-membered heterocycle is disordered over two envelope conformations in a 0.35:0.65 ratio.
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spelling pubmed-29615292010-12-30 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide Shishkina, Svetlana V. Shishkin, Oleg V. Ukrainets, Igor V. Bereznyakova, Nataliya L. Davidenko, Alexandra A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(21)BrN(2)O(5), conjugation between the π-donating N—C—O fragment and the π-withdrawing carbonyl group results in considerable redistribution of the electron density within the dihydropyridinol ring. This effect is also promoted by the formation of an intra­molecular N—H⋯O hydrogen bond. The five-membered heterocycle is disordered over two envelope conformations in a 0.35:0.65 ratio. International Union of Crystallography 2008-05-10 /pmc/articles/PMC2961529/ /pubmed/21202555 http://dx.doi.org/10.1107/S1600536808013378 Text en © Shishkina et al. 2008 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
Shishkina, Svetlana V.
Shishkin, Oleg V.
Ukrainets, Igor V.
Bereznyakova, Nataliya L.
Davidenko, Alexandra A.
2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title_full 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title_fullStr 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title_full_unstemmed 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title_short 2-Bromo­methyl-N-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
title_sort 2-bromo­methyl-n-isopropyl-7,8-dimeth­oxy-1,2-dihydro-1,3-oxazolo[3,2-a]quinoline-4-carboxamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961529/
https://www.ncbi.nlm.nih.gov/pubmed/21202555
http://dx.doi.org/10.1107/S1600536808013378
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