http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200410694-A

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filingDate 2002-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f364ad52ec99375f87b7c3eeed814783
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d00f2c6fc35e6daef3db13bada667b97
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c60805f782cac4bc4eb2fa2f8caec44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_351f4e167a655ac8a3edb68eb642c540
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publicationDate 2004-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200410694-A
titleOfInvention Therapeutic agents
abstract The present invention relates to compounds of formula I, and pharmaceutically acceptable salts, prodrugs, solvates and crystalline forms thereof, in which R1 and R2 independently represent: a C1-6alkyl group; an (amino)C1-4alkyl-group in which the amino is optionally substituted by one or more C1-3alkyl groups; an optionally substituted non-aromatic C3-15carbocyclic group; a (C3-12cycloalkyl)C1-3alkyl-group; a group-(CH2)r(phenyl)s in which r is 0, 1, 2, 3 or 4, s is 1 when r is 0 otherwise s is 1 or 2 and the phenyl groups are optionally independently substituted by one, two or three groups represented by Z; naphthyl; anthracenyl; a saturated 5 to 8 membered heterocyclic group containing one nitrogen and optionally one of the following: oxygen, sulphur or an additional nitrogen wherein the heterocyclic group is optionally substituted by one or more C1-3alkyl groups, hydroxy or benzyl; 1-adamantylmethyl; a group-(CH2)t Het in which t is 0, 1, 2, 3 or 4, and the alkylene chain is optionally substituted by one or more C1-3alkyl groups and Het represents an aromatic heterocycle optionally substituted by one, two or three groups selected from a C1-5alkyl group, a C1-5alkoxy group or halo; or R1 represents H and R2 is as defined above; or R1 and R2 together with the nitrogen atom to which they are attached represent a saturated 5 to 8 membered heterocyclic group containing one nitrogen and optionally one of the following: oxygen, sulphur or an additional nitrogen; wherein the heterocyclic group is optionally substituted by one or more C1-3alkyl groups, hydroxy or benzyl; X is CO or SO2; Y is absent or represents NH optionally substitututed by a C1-3alkyl group; R3 and R4 independently represent phenyl, thienyl or pyridyl each of which is optionally substituted by one, two or three groups represented by Z; Z represents a C1-3alkyl group, a C1-3alkoxy group, hydroxy, halo, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, trifluoromethylsulphonyl, nitro, amino, mono or di C1-3alkylamino, mono or di C1-3alkylamido, C1-3alkylsulphonyl, C1-3alkoxycarbonyl, carboxy, cyano, carbamoyl, mono or di C1-3alkyl carbamoyl, sulphamoyl and acetyl; and R5 is H, a C1-3alkyl group, a C1-3alkoxymethyl group, trifluoromethyl, a hydroxyC1-3alkyl group, C1-3alkoxycarbonyl, carboxy, cyano, carbamoyl, mono or di C1-3alkylcarbamoyl, acetyl, or hydrazidocarbonyl optionally substituted by R1 and R2 where R1 and R2 are as previously defined and; with the proviso that when R1 and R2 together with the nitrogen atom to which they are attached represent 4-methylpiperazin-1-yl or R1 represents H and R2 represents methyl or 1-benzylpiperidin-4-yl; X is CO; Y is absent and R5 is H; then R3 and R4 do not both represent 4-methoxyphenyl; processes for preparing such compounds, their use in the treatment of obesity, psychiatric and neurological disorders, to methods for their therapeutic use and to pharmaceutical compositions containing them.
priorityDate 2001-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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