http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200911770-A

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filingDate 2008-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd3ac0c4c352e4f00697aabb72adc846
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e270f10d39402275f46e16b80d5c0bb4
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publicationDate 2009-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200911770-A
titleOfInvention Piperidine/piperazine derivatives
abstract The invention relates to a DGAT inhibitor of formula including any stereochemically isomeric form thereof, wherein A represents CH or N; X represents O or NRx; the dotted line represents an optional bond in case A represents a carbon atom; Y represents a direct bond; -NRx-C(=O)-; -C(=O)-NRx-; -NRx-C(=O)-Z-; -NRx-C(=O)-Z-NRy-; -NRx-C(=O)-Z-NRy-C(=O)-; -NRx-C(=O)-Z-NRy-C(=O)-O-; -NRx-C(=O)-Z-O-; -NRx-C(=O)-Z-O-C(=O)-; -NRx-C(=O)-Z-C(=O)-; -NRx-C(=O)-Z-C(=O)-O-; -NRx-C(=O)-O-Z-C(=O)-; -NRx-C(=O)-O-Z-C(=O)-O-; -NRx-C(=O)-O-Z-O-C(=O)-; -NRx-C(=O)-Z-C(=O)-NRy-; -NRx-C(=O)-Z-NRy-C(=O)-NRy-; -C(=O)-Z-; -C(=O)-Z-O-; -C(=O)-NRx-Z-; -C(=O)-NRx-Z-O-; -C(=O)-NRx-Z-C(=O)-O-; -C(=O)-NRx-Z-O-C(=O)-; -C(=O)-NRx-O-Z-; -C(=O)-NRx-Z-NRy-; -C(=O)-NRx-Z-NRy-C(=O)-; -C(=O)-NRx-Z-NRy-C(=O)-O-; R1 represents optionally substituted C1-12alkyl; C2-6alkenyl; C2-6alkynyl; C3-6cycloalkyl; aryl1; aryl1C1-6alkyl; Het1; or Het1C1-6alkyl; provided that when Y represents -NRx-C(=O)-Z-; -NRx-C(=O)-Z-NRy; -NRx-C(=O)-Z-C(=O)-NRy-; -C(=O)-Z-; -NRx-C(=O)-Z-NRy-C(=O)-NRy-; -C(=O)-NRx-Z-; -C(=O)-NRx-O-Z-; or -C(=O)-NRx-Z-NRy-; then R1 may also represent hydrogen; R2 and R3 each independently represent hydrogen; hydroxyl; carboxyl; halo; C1-6alkyl; polyhaloC1-6alkyl; C1-6alkyloxy optionally substituted with C1-4alkyloxy; C1-6alkylthio; polyhaloC1-6alkyloxy; C1-6alkyloxycarbonyl; cyano; aminocarbonyl; mono-or di(C1-4alkyl)aminocarbonyl; C1-6alkylcarbonyl; nitro; amino; mono-or di(C1-4alkyl)amino; -S(=O)p-C1-4alkyl; R4 represents hydrogen; hydroxyl; carboxyl; halo; C1-6alkyl; polyhaloC1-6alkyl; optionally substituted C1-6alkyloxy; C1-6alkylthio; polyhalo-C1-6alkyloxy; C1-6alkyloxycarbonyl wherein C1-6alkyl may optionally be substituted; cyano; C1-6alkylcarbonyl; nitro; amino; mono-or di(C1-4alkyl)amino; C1-4alkylcarbonylamino; -S(=O)p-C1-4alkyl; R6R5N-C(=O)-; R6R5N-C1-6alkyl; C3-6cycloalkyl; aryl; aryloxy; arylC1-4alkyl; aryl-C(=O)-C1-4alkyl; aryl-C(=O)-; Het; HetC1-4alkyl; Het-C(=O)-C1-4alkyl; Het-C(=O)-; Het-O-; R9 represents hydrogen, halo, C1-4alkyl, C1-4alkyl substituted with hydroxyl; a N-oxide thereof, a pharmaceutically acceptable salt thereof or a solvate thereof. The invention further relates to methods for preparing such compounds, pharmaceutical compositions comprising said compounds as well as the use as a medicine of said compounds.
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priorityDate 2007-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 560.