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, C14H13ClN2O2S, 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 dimer...
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International Union of Crystallography
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doaj-907a00dbef8449a898f303b7c043e92e2020-11-24T22:16:16ZengInternational Union of CrystallographyActa Crystallographica Section E: Crystallographic Communications2056-98902015-06-0171666066210.1107/S2056989015008099wm5147Crystal structure of 1-[(6-chloropyridin-3-yl)sulfonyl]-1,2,3,4-tetrahydroquinolineS. Jeyaseelan0H. R. Rajegowda1R. Britto Dominic Rayan2P. Raghavendra Kumar3B. S. Palakshamurthy4Department of Physics, St Philomena's College (Autonomous), Mysore, Karnataka 570 015, IndiaDepartment of Studies and Research in Chemistry, Tumkur University, Tumkur 572 103, Karnataka, IndiaDepartment of Chemistry, St Philomena's College (Autonomous), Mysore, Karnataka 570 015, IndiaDepartment of Studies and Research in Chemistry, Tumkur University, Tumkur 572 103, Karnataka, IndiaDepartment of Studies and Research in Physics, U.C.S, Tumkur University, Tumkur, Karnataka 572 103, IndiaThe tetrahydropyridine ring of the quinoline system in the title compound, C14H13ClN2O2S, 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 R22(10) loops. Additional intermolecular C—H...O hydrogen bonds generate C(7) chains along [100].http://scripts.iucr.org/cgi-bin/paper?S2056989015008099crystal structure1,2,3,4-tetrahydroquinolineC—H...O interactionspharmacological activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Jeyaseelan H. R. Rajegowda R. Britto Dominic Rayan P. Raghavendra Kumar B. S. Palakshamurthy |
spellingShingle |
S. Jeyaseelan H. R. Rajegowda R. Britto Dominic Rayan P. Raghavendra Kumar B. S. Palakshamurthy Crystal structure of 1-[(6-chloropyridin-3-yl)sulfonyl]-1,2,3,4-tetrahydroquinoline Acta Crystallographica Section E: Crystallographic Communications crystal structure 1,2,3,4-tetrahydroquinoline C—H...O interactions pharmacological activity |
author_facet |
S. Jeyaseelan H. R. Rajegowda R. Britto Dominic Rayan P. Raghavendra Kumar B. S. Palakshamurthy |
author_sort |
S. Jeyaseelan |
title |
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_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_sort |
crystal structure of 1-[(6-chloropyridin-3-yl)sulfonyl]-1,2,3,4-tetrahydroquinoline |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E: Crystallographic Communications |
issn |
2056-9890 |
publishDate |
2015-06-01 |
description |
The tetrahydropyridine ring of the quinoline system in the title compound, C14H13ClN2O2S, 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 R22(10) loops. Additional intermolecular C—H...O hydrogen bonds generate C(7) chains along [100]. |
topic |
crystal structure 1,2,3,4-tetrahydroquinoline C—H...O interactions pharmacological activity |
url |
http://scripts.iucr.org/cgi-bin/paper?S2056989015008099 |
work_keys_str_mv |
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