The invention belongs to the field of
organic synthesis, and discloses a method for catalytically preparing a
drug intermediate chromene pyrimido indazolone derivative, which comprises the following steps: adding an
ethanol water solution into a reaction container, adding aromatic
aldehyde, 1H-
indazole-3-amine and 4-hydroxycoumarin, stirring at
room temperature, uniformly mixing, and finally adding an acidic
ionic liquid catalyst; heating until the
solvent flows back, keeping the temperature until the
raw material point disappears, and stopping stirring after the reaction is finished; coolingthe reaction solution to
room temperature,
grinding the precipitated
solid, performing standing, and carrying out suction
filtration to obtain filter residues; washing the filter residue with
ethanol,and carrying out
vacuum drying to obtain a product; and adding reaction raw materials into the filtrate after suction
filtration to carry out the next round of reaction. According to the method, thenew acidic
ionic liquid catalyst is utilized, and the
ethanol aqueous solution is used as a reaction
solvent, so that the catalytic reaction efficiency can be effectively improved, the adding amount of the catalyst is reduced, the ethanol
aqueous solution can effectively play a role of a recrystallization
solvent, and the purification process is simplified.