A series of pyrazole-based heteroaromatic compounds were synthesized by the reaction of
3-methyl-5-pyrazolone and aromatic aldehydes in Choline chloride/urea DES as a green solvent. This
simple and green procedure has advantages such as easy operation, short reaction times, efficient
yields, low cost and minimum use of hazardous solvents and catalysts. The structure of compounds
was determined by IR, 1H and 13C NMR spectra, and the crystal structure of 4a was confirmed using
X-ray crystallographic analysis. The optical properties of Pyrazole derivatives 4a-g have also been
studied with UV/vis and fluorescence spectroscopy. All of these pyrazole-containing heteroaromatic
compounds displayed maximum emission peak from 340 to 360 nm.
Keywords: Pyrazolone, Fluorescence, Deep eutectic solvent (DES), Choline chloride/urea, Multi-component reaction, Knovenagel
condensation, Michael addition.
Kidwai, M.; Mohan, R.G.J. Korean. Chem. Soc., 2004, 48, 177-181.
Rahat Khan, M.D.; Imam Uddin, M.D. Bangladesh J. Pharmacol., 2008, 3, 27-35.
X-STEP32 Version1.07b, X-ray structure evaluation package; Stoe&Cie: Darmstadt, Germany, 2000.
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