Gliquidone
The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N—H...O=S interaction, as well as intermolecular N—H...O=C hydrogen bond...
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2011-06-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536811016680 |
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doaj-0f47f1c5d31f4fd5954aeba0ee4e994c |
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doaj-0f47f1c5d31f4fd5954aeba0ee4e994c2020-11-25T03:05:25ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-06-01676o1343o134310.1107/S1600536811016680GliquidoneThomas GelbrichMairi F. HaddowUlrich J. GriesserThe title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N—H...O=S interaction, as well as intermolecular N—H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603–11610].http://scripts.iucr.org/cgi-bin/paper?S1600536811016680 |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Thomas Gelbrich Mairi F. Haddow Ulrich J. Griesser |
| spellingShingle |
Thomas Gelbrich Mairi F. Haddow Ulrich J. Griesser Gliquidone Acta Crystallographica Section E |
| author_facet |
Thomas Gelbrich Mairi F. Haddow Ulrich J. Griesser |
| author_sort |
Thomas Gelbrich |
| title |
Gliquidone |
| title_short |
Gliquidone |
| title_full |
Gliquidone |
| title_fullStr |
Gliquidone |
| title_full_unstemmed |
Gliquidone |
| title_sort |
gliquidone |
| publisher |
International Union of Crystallography |
| series |
Acta Crystallographica Section E |
| issn |
1600-5368 |
| publishDate |
2011-06-01 |
| description |
The title compound {systematic name: N-cyclohexylcarbamoyl-4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxo-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]benzenesulfonamide}, C27H33N3O6S, displays an intramolecular N—H...O=S interaction, as well as intermolecular N—H...O=C hydrogen bonds. The latter interactions lead to the formation of hydrogen-bonded chains parallel to the c axis. The conformation of the sulfonylurea fragment is in agreement with a recent theoretical study [Kasetti et al. (2010). J. Phys. Chem. B, 114, 11603–11610]. |
| url |
http://scripts.iucr.org/cgi-bin/paper?S1600536811016680 |
| work_keys_str_mv |
AT thomasgelbrich gliquidone AT mairifhaddow gliquidone AT ulrichjgriesser gliquidone |
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1724678666233839616 |