FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes a novel cyclic ether of the formula (I) where each R1 and R2 means hydrogen atom, lower alkyl or C1-6-alkylcarbonyl; R3, R4, R5 each means lower alkyl; R6 means lower alkyl; Ar means C6-14-aryl that can be substituted with halogen atom, C1-6-alkyl, C1-6-alkoxy-group or C1-3-alkylenedioxy-group; ring A means 5-8-membered saturated nitrogen-containing heterocyclic ring; X means lower alkylene; Y means carbon or nitrogen atom; Za means the group of formulas (a) , (b) , (c) or (d) where R7 means hydrogen atom or C6-14-aryl that can be substituted with halogen atom or C1-6-alkoxy-group; R10 means hydrogen atom or C7-16-aralkyl; Zb means a bond or bivalent hydrocarbon group taken among the group including C1-8-alkylene, C2-8-alkenylene or group of the formula: -(CH2)p-M-(CH2)q- where p and q each means a whole number from 0 to 8 and p + q means a whole number from 1 to 8; M means O or NR9 where R9 means hydrogen atom being each bivalent group can be substituted with C6-14-aryl; and m means a whole number from 1 to 3, or its salt that can be used for preparing pharmaceutical composition used for sodium channel modulation. Invention describes method of synthesis of ether, pharmaceutical composition and method of modulation of sodium channel activity. EFFECT: new cyclic ether indicated above, improved method of synthesis, valuable pharmacological properties of ether. 26 cl, 5 tbl
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