FIELD: organic chemistry. SUBSTANCE: product: derivatives of benzopyran of the formula (I) where R1, R2, α-β, R3 and R4 have corresponding meanings. Reagent 1: compound of the formula (IV) where a) W W-NH2--group; W′-OH- OH-group or b) W and W′ together with oxygen atom form ethoxy-group. Reagent 2: in the case of a) compound of the formula (V) where R4 as indicated above; R6 C1-C4-alkyl; R7 formyl or haloidmethyl, or in the case of b) compound of the formula (VI) or (VIa) where R4 and R5 as indicated above; Q -α-γ- represents a group of the formula (VII) or (VIII) where R8a, R8b and R8c C1-C4--alkyl, and compound of the formula (Ia) is synthesized where R1 and R2 as indicated above. If necessary, compound of the formula (Ia) is treated with base, and compound of the formula (Ib) is prepared where R1 and R2 as indicated above, or, if necessary, compound of the formula (Ia) is interacted with nitrating reagent, and compound of the formula (Ic) is prepared where R1 and R2 as indicated above, or, if necessary, compounds of the formulas (Ia) (Ib) and (Ic) were isolated in the form of pharmaceutically acceptable salt. Realative activity of synthesized compounds as compared with cromacalim is 17-64% Synthesized compounds were used in medicine. EFFECT: improved method of synthesis. 4 cl, 3 tbl
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Authors
Dates
1995-06-27—Published
1991-10-23—Filed