FIELD: medicine. SUBSTANCE: described are new heteroaryloxyethyl amines of general formula: wherein Ar is bicyclic heteroaryl containing one or two nitrogen atoms optionally substituted by hydroxy, halogen or lower alkyl, Y is C(O)NH- or NHC(O), R is lower alkyl, C3-C6 cycloalkyl optionally substituted by lower alkyl, or phenyl or salts of said compounds. Also described are method of preparing said compounds, pharmaceutical composition comprising said compounds having affinity to 5HT1A receptors, and intermediate compounds of formula V: wherein Ar, Y and R are as defined in claim 1. Invention is useful in medicine as gastic acid secretion inhibitors or as antivoming agents. EFFECT: improved properties of the pharmaceutical composition. 15 cl, 2 ex, 2 tbl
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