Acta Cryst. (2011). E67, o1343 [ doi:10.1107/S1600536811016680 ]
Abstract: 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-HO=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].
 |   Hyper-Text Markup Language (HTML) file (82.1 kbytes) |
 | Chemical Markup Language (CML) file (10.2 kbytes) |
To open or display or play some files, you may need to set your browser up to use the appropriate software. See the full list of file types for an explanation of the different file types and their related mime types and, where available links to sites from where the appropriate software may be obtained.
The download button will force most browsers to prompt for a file name to store the data on your hard disk.
Where possible, images are represented by thumbnails.
Copyright © International Union of Crystallography
IUCr Webmaster