Crystal structure and synthesis of 4-(4-hydroxybenzylideneamino)-1-methyl-3-propyl-1 H-pyrazole-5-carboxamide

Abstract

The title compound C 15H 18N 4O 2 ( I), was prepared from the reaction of 4-amino-1-methyl-3-propyl-1 H-pyrazole-5-carboxamide and 4-hydroxybenzaldehyde; and was analyzed by analytical data from 1H NMR, 13C NMR, IR and Mass spectra. The crystal structure was determined by single crystal X-ray diffraction. The molecules in the crystal structure form cyclic centrosymmetric supramolecular tetramer synthons [graph-set R 4 4 ( 12 ) ] through amide N–H⋯O(hydroxy) and hydroxy O–H⋯O(amide) hydrogen bonds to form perpendicular tapes.