FIELD: organic chemistry. SUBSTANCE: product: hydroxyalkylfuran derivatives of the formula (I) given in description text, - pharmaceutically acceptable salt of acid association of its or stereoisomeric compound where -A1-A2-A3-A4- - divalent radical with formula: -CH=CH-CH=CH- (a-1), -N=CH-CH=CH- (a-2), -CH=CH-CH=N- (a-5) or -N=CH-N=CH- (a-6), n=1 or 2B-NR4 or CH2; R4 - H or C1-C6-alkyl; L - H, C1-C6-alkyl, C1-C6-alkylhydroxycarbonyl, or radical of the formula: -Alk-R5 (b-1); -Alk-Y-R6 (b-2), -Alk-Z1-C(=X)-Z2-R7 (b-3), or -CH2-CHOH-CH2-O-R8 (b-4) where R5 - cyano-group, phenyl which does not obligatory substituted with alkoxy-C1-C6; pyridinyl; 4,5-dihydro-5- oxo-1H-tetrazolyl; 2-oxo-3-oxazolidinyl; 2,3-dihydro-2 -oxo-1H-benzimidazolyl; or bicyclic radical of the formula (c-4-a) where G2 - -CH=CH-CH=CH-, -S-(CH2)3-, -S-(CH2)2-, -S-CH= CH- or -CH=C(CH3)-O--group; R6-C1-C6 - R7-C1-C6-alkyl; pyridinyl which does not obligatory substituted with nitro-group; pyrimidinyl; pyrazinyl; pyridazinyl; 2,3-dihydro-3-oxopyridazinyl which does not obligatory substituted with halogen; or 9-methyl-6-purinyl; R8-alkyl; haloidphenyl; Y - O or NH, Z1 or Z2 every independently is NH or direct bond, X - O, every Alk is independently C1-6-alkanediyl. Synthesized compounds were used in medicine. EFFECT: improved method of synthesis. 2 cl, 8 tbl
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