FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula (I)
,
where: each R1, R1a and R2 is independently selected from the group consisting of H, halogen, OH, CN, CF3, OCF3, OCH3, CH2OH, C3cycloalkyloxy, COOH, CONR3R4 and tetrazole; Ar is a group of the following formula:
,
e is an integer selected from the group consisting of 0, 1, 2, 3 and 4; f e is an integer selected from the group consisting of 0, 1, 2 and 3; where each R8 is independently selected from the group consisting of H, halogen, methoxy, OCF3, OCF2H, isopropoxy, methyl, propyl, 4-fluorophenyl, thiophene, furan, 5-fluorofuran, 5-fluorothiophene, 5-chlorothiophene, 5-chlorofuran, OSO2CF3, OSO2CH3, cyclopropyl and cyclopropyloxy; where R9 is selected from the group consisting of H and methyl; A is -CRaRb-; B represents a group of the formula -(CRcRd)n-; where each Ra and Rb is independently selected from the group consisting of H, methyl, ethyl, isopropyl, cyclopropyl, phenyl, 4-chlorophenyl, 4-fluorophenyl and thiophen-2-yl; where Rc and Rb are both H; where each R3 and R4 is H, n is an integer selected from the group consisting of 0 and 1; a is an integer selected from the group consisting of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10.
EFFECT: compounds that are capable of inhibiting 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) and which are useful in the treatment of conditions such as non-insulin-dependent diabetes mellitus type 2 (NIDDM), insulin resistance, obesity, dyslipidemia.
20 cl, 1 tbl, 238 ex
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Authors
Dates
2018-11-15—Published
2012-12-21—Filed