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Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline

The tetra­hydro­pyridine ring of the quinoline system in the title compound, C(14)H(13)ClN(2)O(2)S, adopts a half-chair conformation with the bond-angle sum at the N atom being 350.0°. The dihedral angle between the least-squares planes of the two aromatic rings is 50.13 (11)°. In the crystal, inver...

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Autores principales: Jeyaseelan, S., Rajegowda, H. R., Britto Dominic Rayan, R., Raghavendra Kumar, P., Palakshamurthy, B. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459366/
https://www.ncbi.nlm.nih.gov/pubmed/26090144
http://dx.doi.org/10.1107/S2056989015008099
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author Jeyaseelan, S.
Rajegowda, H. R.
Britto Dominic Rayan, R.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
author_facet Jeyaseelan, S.
Rajegowda, H. R.
Britto Dominic Rayan, R.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
author_sort Jeyaseelan, S.
collection PubMed
description The tetra­hydro­pyridine ring of the quinoline system in the title compound, C(14)H(13)ClN(2)O(2)S, adopts a half-chair conformation with the bond-angle sum at the N atom being 350.0°. The dihedral angle between the least-squares planes of the two aromatic rings is 50.13 (11)°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(10) loops. Additional inter­molecular C—H⋯O hydrogen bonds generate C(7) chains along [100].
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spelling pubmed-44593662015-06-18 Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline Jeyaseelan, S. Rajegowda, H. R. Britto Dominic Rayan, R. Raghavendra Kumar, P. Palakshamurthy, B. S. Acta Crystallogr E Crystallogr Commun Research Communications The tetra­hydro­pyridine ring of the quinoline system in the title compound, C(14)H(13)ClN(2)O(2)S, adopts a half-chair conformation with the bond-angle sum at the N atom being 350.0°. The dihedral angle between the least-squares planes of the two aromatic rings is 50.13 (11)°. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(10) loops. Additional inter­molecular C—H⋯O hydrogen bonds generate C(7) chains along [100]. International Union of Crystallography 2015-05-23 /pmc/articles/PMC4459366/ /pubmed/26090144 http://dx.doi.org/10.1107/S2056989015008099 Text en © Jeyaseelan et al. 2015 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 Research Communications
Jeyaseelan, S.
Rajegowda, H. R.
Britto Dominic Rayan, R.
Raghavendra Kumar, P.
Palakshamurthy, B. S.
Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title_full Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title_fullStr Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title_full_unstemmed Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title_short Crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
title_sort crystal structure of 1-[(6-chloro­pyridin-3-yl)sulfon­yl]-1,2,3,4-tetra­hydro­quinoline
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459366/
https://www.ncbi.nlm.nih.gov/pubmed/26090144
http://dx.doi.org/10.1107/S2056989015008099
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