FIELD: organic chemistry, chemical technology, pharmacy. SUBSTANCE: invention describes the novel compounds of the formula (1) where Z means saturated or unsaturated chain consisting of 3-6 carbon atoms; m = 2 or 3; R1 means hydrogen atom or linear or branched C1-4-alkyl; R2, R3 and R13 are located in ortho-, meta- or para-position of phenyl ring and they are similar or distinct and are taken from the following groups: H, OH, OR14, halogen atom, CO2R9, CN, where R9, R12 and R14 mean linear or branched C1-4-alkyl; R10 and R11 are similar or distinct and mean hydrogen atom or linear or branched C1-6-alkyl where R means the group of the formula (Ia) where R4 and R5 are similar or distinct; when they are distinct then mean hydrogen atom, linear or branched C1-5-alkyl or substituted or unsabstituted cycloalkyl; when they are similar then mean linear or branched C1-5-alkyl or R4 and R5 in common form the group -(CH2)n1- where n1 = 3-7, or the formula (2) where R6 means hydrogen atom or linear or branched C1-6-alkyl and R7 means substituted or unsubstituted cycloalkyl or R6 and R7 in common form the group -(CH2)n2- where n2 = 3-6, or the formula (3) where W means optional substituted carbocyclic ring (or rings) or optional substituted methylene group and R8 means linear or branched C1-5-alkyl or phenyl; n3 = 0-2, or the formula (4) where W means optional substituted carbocyclic ring (rings) or optional substituted methylene group and n4 = 1 or 2 in racemic or optically active form, or their pharmaceutically acceptable salts. Invention describes a method of synthesis of the above indicated compounds and a pharmaceutical preparation based on compounds of the formula (1). The novel compounds can be used for treatment of patients with psychiatric disorders, for example, schizophrenia and other psychosis, pathological fear, depression and circular psychosis. EFFECT: improved method of synthesis, antipsychotic activity of compounds. 12 cl, 1 tbl, 49 ex
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