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filingDate 1999-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cca876413af4e3b23e39558b395db7b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5b604f0e61ac22c8edda85c180ed9b9
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publicationDate 2002-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-495510-B
titleOfInvention Novel naphthyridine derivatives, the preparation processes and the pharmaceutical compositions thereof
abstract Compounds of formula (I) and pharmaceutically acceptable salts and solvates: where R1 is hydrogen, C1-6 alkyl (optionally substituted by hydroxy or C1-4 alkoxy), phenyl-C1-4 alkyl, C1-6 alkenyl, C1-6 alkynyl; R2 is hydrogen or up to three substituents selected from halogen, NO2, CN, N3, CF3O-, CF3S-, CF3SO2-, CF3CO-, C1-6 alkyl, C1-6 alkenyl, C1-6 alkynyl, C1-6 perfluoroalkyl, C3-6 cycloalkyl, C3-6cycloalkyl-C1-4alkyl-, C1-6alkylO-, C1-6alkylCO-, C3-6cycloalkylO-, C3-6cycloalkylCO-, C3-6cycloalkyl-C1-4alkylO-, C3-6cycloalkyl-C1-4alkylCO-, phenyl, phenoxy, benzyloxy, benzoyl, phenyl-C1-4alkyl-, C1-6alkylS-, C1-6alkylSO2, (C1-4alkyl)2NSO2-, (C1-4alkyl)NHSO2-, (C1-4alkyl)2NCO-, (C1-4alkyl)NHCO- or CONH2; or -NR5R6 where R5 is hydrogen or C1-4 alkyl, and R6 is hydrogen, C1-4 alkyl, formyl, -CO2C1-4alkyl or -COC1-4alkyl; or two R2 groups together form a carbocyclic ring that is saturated or unsaturated, optionally interrupted by O or NH; R3 groups and R4 groups are each independently hydrogen or C1-6 alkyl and/or the two R3 groups and/or the two R4 groups together form a C3-6 spiroalkyl group, provided that at least one R3 or R4 group is not hydrogen; and X is selected from hydrogen, halogen, cyano, alkyl and alkoxy, are useful in the treatment and prophylaxis of epilepsy, migraine, and other disorders.
priorityDate 1998-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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