![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Buy article online]](/logos/buy.gif)
![[Contents scheme]](ya2010contents.gif)
Acta Cryst. (2006). E62, o2306-o2307 [ doi:10.1107/S1600536806017089 ]
Abstract: The title compound, C26H21ClN4O2, has been synthesized by the reaction of 4-(4-chlorobenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one with 3-methyl-1-phenyl-1H-pyrazol-5-amine in glycol under microwave irradiation. All atoms of the pyrazolo[3,4-b]pyridine system, with the exception of two adjacent C atoms carrying the benzamido and oxo substituents (positions 5 and 6), lie in one plane; the displacements of the latter C atoms from this plane are 0.284 (5) and 0.847 (5) Å respectively. Only one of the two NH groups, viz. that in the dihydropyridinone ring, participates in the intermolecular hydrogen bonds which link the molecules into infinite chains running along the b axis
Online 12 May 2006
Copyright © International Union of Crystallography
IUCr Webmaster