
Acta Cryst. (2012). E68, o1136 [ doi:10.1107/S1600536812010872 ]
Abstract: The title compound, C19H19N3O4S2, was prepared by the reaction of 2,3-diaminopyridine with tosyl chloride in a mixture of dichloromethane-pyridine as solvent. In the crystal, molecules associate via pairs of N-H
N hydrogen bonds, forming a centrosymmetric eight-membered {
HNCN}2 synthon. The dihedral angles between the aminopyridine ring and the tosyl benzene rings are 50.01 (6) and 32.01 (4)°.
![]() ![]() Hyper-Text Markup Language (HTML) file (75.4 kbytes) | |
![]() ![]() Chemical Markup Language (CML) file (7.2 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