发明名称 Mchir antagonists
摘要 The present invention provides compounds of formula (I), wherein R<SUP>1 </SUP>represents a C<SUB>1-4 </SUB>alkoxy group optionally substituted by one or more fluoro or a C<SUB>1-4</SUB>alkyl group optionally substituted by one or more fluoro; n represents 0 or 1; R<SUP>2 </SUP>represents a C<SUB>1-4</SUB>alkyl group optionally substituted by one or more fluoro or a C<SUB>1-4</SUB>alkoxy group optionally substituted by one or more fluoro; m represents 0 or 1; R<SUP>3 </SUP>represents H or a C<SUB>1-4</SUB>alkyl group; L<SUP>1 </SUP>represents an alkylene chain (CH<SUB>2</SUB>)<SUB>r </SUB>in which r represents 2 or 3 or L<SUP>1 </SUP>represents a cyclohexyl group wherein the two nitrogens bearing R<SUP>3 </SUP>and R<SUP>4</SUP>, respectively, are linked to the cyclohexyl group either via the 1,3 or the 1,4 positions of the cyclohexyl group or L<SUP>1 </SUP>represents a cyclopentyl group wherein the two nitrogens bearing R<SUP>3 </SUP>and R<SUP>4</SUP>, respectively, are linked to the cyclopentyl group via the 1,3 position of the cyclopentyl group and additionally when R<SUP>5 </SUP>represents 9,10-methanoanthracen-9(10H)-yl the group -L<SUP>1</SUP>-N(R<SUP>4</SUP>)- together represents a piperidyl ring which is linked to L<SUP>2 </SUP>through the piperidinyl nitrogen and to N-R<SUP>3 </SUP>via the 4 position of the piperidyl ring with the proviso that when R<SUP>5 </SUP>represents 9,10-methanoanthracen-9(10H)-yl then r is only 2; R<SUP>4 </SUP>represents H or a C<SUB>1-4</SUB>alkyl group optionally substituted by one or more of the following: an aryl group or a heteroaryl group; L<SUP>2 </SUP>represents a bond or an alkylene chain (CH<SUB>2</SUB>), in which s represents 1, 2 or 3 wherein the alkylene chain is optionally substituted by one or more of the following: a C<SUB>1-4</SUB>alkyl group, phenyl or heteroaryl; R<SUP>5 </SUP>represents aryl, a heterocyclic group or a CH<SUB>3-8</SUB>cycloalkyl group which is optionally fused to a phenyl or to a heteroaryl group; as well as optical isomers and racemates thereof as well as pharmaceutically acceptable salts, thereof; with provisos, processes for preparing such compounds, their use in the treatment of obesity, psychiatric disorders, cognitive disorders, memory disorders, schizophrenia, epilepsy, and related conditions, and neurological disorders such as dementia, multiple sclerosis, Parkinson's disease, Huntington's chorea and Alzheimer's disease and pain related disorders and to pharmaceutical compositions containing them.
申请公布号 US2006247439(A1) 申请公布日期 2006.11.02
申请号 US20030520372 申请日期 2003.07.04
申请人 ASTRAZENECA AB 发明人 RAY ASIM K.;EVERTSSON EMMA M.;LINUSSON JONSSON ANNA STINA M.;SANDBERG PERNILLA M.;INGIIARDT TORD;SVENSSON ANETTE M.;BRICKMANN KAY
分类号 A61K31/4709;C07D215/38;A61K31/47;A61K31/4706;A61P3/04;A61P25/00;C07D401/02;C07D401/12;C07D405/02;C07D405/12;C07D407/12;C07D409/02;C07D409/12 主分类号 A61K31/4709
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