FIELD: organic chemistry, chemical technology, medicine, biochemistry, pharmacy. SUBSTANCE: invention relates to novel N-phenylamide and N-pyridylamide derivatives of the formula (I): wherein X means oxygen or sulfur atom; R1 and R2 that can be similar or different mean hydrogen atom, (C1-C6)-alkyl or (C3-C8)- cycloalkyl; or R1 and R2 in common with carbon atom to which they are bound form (C3-C8)-cycloalkyl; R3 means (C6-C12)-aryl optionally substituted with one or some radicals Y that can be similar or different; Y means halogen atom; R4 and R5 mean hydrogen atom; Ar means one of the following groups: (B) or (C) ; T means hydrogen atom or (C1-C6)-alkyl; T3 and T4 that can be similar or different mean (C1-C6)- alkyl, (C1-C6)-alkoxy-group, (C1-C6)-alkylthio-group; R6 and R7 each means hydrogen atom; or R6 and R7 in common mean a bond; Z means either (I) bivalent group wherein R9 means hydrogen atom or - alkyl or (II) bivalent group wherein R10 and R11 in common form such bond that Z means group CH= CH-; or R10 and R11 that can be similar or different have values indicated above for R9; or (III) bivalent group wherein R12 and R13 in common form such bond that Z means CH=CH-; or R12 and R13 that can be similar or different have values indicated above for R9 as well to its additive salts with pharmaceutically acceptable acid or bases. Invention relates also to method for preparing these compounds, pharmaceutical composition and medicinal agent eliciting hypolipidemic and anti- - atherosclerotic effect based on thereof. These compounds are inhibitors of cholesterol-acyltransferase (ACAT) and can be used in medicine. Invention provides preparing novel N-phenylamide and N- pyridylamide derivatives eliciting valuable biologically active effect. EFFECT: improved preparing method, valuable medicinal properties. 15 cl, 10 tbl, 17 ex
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Authors
Dates
2003-10-20—Published
1998-12-11—Filed