FIELD: chemistry.
SUBSTANCE: invention relates to a method of producing furo[3,4-c]pyridine-3(1H)-one derivatives of general formula (1), where X=Cl, R1=R2=CH3; X=Cl, R1=R2=C6H5; X=Cl, R1+R2=(CH2)4; X=Br, R1=R2=CH3, which involves reacting corresponding 5,6-disubstituted 2-halopyridine-3,4-dicarboxylic acids with propionic anhydride while heating for 10-12 hours and reducing intermediate 4-halogenfuro[3,4-c]pyridine-1,3-dione with sodium borohydride for 3-4 hours at room temperature, followed by evaporating the reaction mass on a rotary evaporator under vacuum, diluting the residue with water, neutralization with 10% aqueous HCl solution, extraction with ethyl acetate, purification of ethyl acetate extracts by column chromatography and recrystallisation of product after chromatography from propan-2-ole.
EFFECT: method of producing novel derivatives of compounds of formula (I), which can be used in medicine for treating or preventing autoimmune and inflammatory diseases, neurological and psychiatric disorders.
1 cl, 4 ex
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Authors
Dates
2020-12-15—Published
2020-06-02—Filed