摘要 |
A compound of Formula (I) and pharmaceutically and/or veterinarily acceptable derivatives thereof, wherein: R<SUP>1</SUP>, R<SUP>2</SUP>, R<SUP>3</SUP> and R<SUP>20 </SUP>are each independently H, CI, Br, F, I, CF<SUB>3</SUB>, OCF<SUB>3</SUB>, Me or Et; R<SUP>4</SUP> is het or C<SUB>3-7 </SUB>cycloalkyl optionally substituted by C<SUB>1-4 </SUB>alkyl, C<SUB>1-4 </SUB>alkoxy, alkoxyalkyl containing 2 to 4 carbon atoms or -S-(C<SUB>1-4 </SUB>alkyl); a is 0 or 1; and het is a non-aromatic 4-, 5- or 6- membered heterocycle which contains at least one N, O or S heteroatom, optionally fused to a 5- or 6- membered carbocyclic group or a second 4-, 5- or 6-membered heterocycle which contains at least one N, O or S heteroatom, wherein the het group is optionally substituted by at least one substituent independently selected from C<SUB>1-8</SUB>alkyl, C<SUB>1-8</SUB>alkoxy, OH, halo, CF<SUB>3</SUB>, OCF<SUB>3</SUB>, SCF<SUB>3</SUB>, hydroxy-C<SUB>1-6</SUB>alkyl, C<SUB>1-4 </SUB>alkoxy-C<SUB>1-6</SUB>alkyl and C<SUB>1-4 </SUB>alkyl-S-C<SUB>1-4</SUB>alkyl; provided that at least one of R<SUP>1</SUP>, R<SUP>2</SUP> and R<SUP>3</SUP> are other than H. The compounds of the invention exhibit activity as both serotonin and noradrenaline re-uptake inhibitors and therefore have utility in a variety of therapeutic areas, for example urinary incontinence. |