摘要 |
The present invention relates to novel compounds of formula (I): wherein - represents a single or a double bond; R is a radical selected from: in which R<SUB>1 </SUB>is halogen, cyano, C<SUB>1-4 </SUB>alkyl, C<SUB>1-4 </SUB>alkoxy, trifluoromethyl or trifluoromethoxy and p is zero or an integer from 1 to 3; R<SUB>2 </SUB>is hydrogen or C<SUB>1-4 </SUB>alkyl; R<SUB>3 </SUB>is hydrogen, hydroxy or C<SUB>1-4 </SUB>alkyl; R<SUB>4 </SUB>is hydrogen or R<SUB>4 </SUB>together with R<SUB>3 </SUB>represents -O or -CH2; R<SUB>5 </SUB>is phenyl, naphthyl, a 9 to 10 membered fused bicyclic heterocyclic group or a 5 or 6 membered heteroaryl group, wherein said groups are optionally substituted by 1 to 3 groups independently selected from trifluoromethyl, C<SUB>1-4 </SUB>alkyl, hydroxy, cyano, C<SUB>1-4 </SUB>alkoxy, trifluoromethoxy, halogen or S(O)qC<SUB>1-4 </SUB>alkyl; R<SUB>6 </SUB>and R<SUB>7 </SUB>independently are hydrogen, cyano, C<SUB>1-4 </SUB>alkyl; R<SUB>8 </SUB>is (CH<SUB>2</SUB>)rR<SUB>10</SUB>; R<SUB>9 </SUB>is hydrogen, halogen, C<SUB>3-7 </SUB>cycloalkyl, hydroxy, nitro, cyano or C<SUB>1-4 </SUB>alkyl optionally substituted by one or two groups selected from halogen, cyano, hydroxy or C<SUB>1-4 </SUB>alkoxy; R<SUB>10 </SUB>is hydrogen or C<SUB>3-7 </SUB>cycloalkyl; n is 1 or 2; q is 0, 1 or 2; r is 0 or an integer from 1 to 4; or a pharmaceutically acceptable salt or a solvate thereof, process for their preparation and their use in the treatment of conditions mediated by tackykinins and/or by selective inhibition of the serotonin reuptake transporter protein
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