FIELD: chemistry.
SUBSTANCE: invention relates to organic synthesis and pharmaceutics, specifically to a method of producing 4-aryl-substituted 7-hydroxy-6'-phenyl-5',6'-dihydro-1'H-spiro[chroman-2,4'-pyrimidine]-2'(3'H)-ones of structural formula (1), which can be used as precursors for synthesis of biologically active substances and medicinal preparations. Method of producing compounds of general formula (1), where R1=H, or Cl, or Me, or MeO, R2=H or Me, is characterized by that the synthesis reagents used are 6-styryl-substituted 4-phenyl-3,4-dihydropyrimidin-2(1H)-ones and resorcins, such as benzene-1,3-diol or 2-methylbenzene-1,3-diol, in molar ratio of 1:2, which react in a solution of chloroform and water in the presence of n-toluenesulphonic acid at temperature of 30–40 °C for 1–3 hours. Obtained reaction mass is cooled, the precipitate is filtered, washed with water, recrystallised from ethyl acetate and dried in air.
EFFECT: providing a method for synthesis of new target spiro[chroman-2,4'-pyrimidine]-2'(3'H)-ones.
1 cl, 8 ex
formula (1)
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Authors
Dates
2024-04-23—Published
2023-10-16—Filed