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filingDate 2000-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_865abff4c943d914b30ede94f978c3b8
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publicationDate 2006-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2246247-T3
titleOfInvention DERIVATIVES OF SULFONIL-CARBOXAMIDE PROCEDURE FOR ITS PREPARATION AND ITS USE AS MEDICATIONS.
abstract Compounds of the ** formula **, in which they mean R1, R2, independently of one another, NR6R7, piperidine, piperazine, tetrahydropyridine, the rings being able to be substituted in each case with phenyl, (C1-C6) alkyl-phenyl, (C1-C8) alkyl, (CO) -C1-C6 alkyl; R6 and R7, independently of each other, H, (C1-C6) alkyl, (C1-C6) alkyl -NH-C1-C6 alkyl, (C1-C6) alkyl -N- [(C1-C6) alkyl ] 2, (CH2) n-Ar, where n can be = 0-6 and Ar can be equal to phenyl, 2-, 3- or 4-pyridyl, piperidinyl, pyrrolidinyl, 2-, 4- or 5-pyrimidinyl, 2 -pyrazinyl, 2-, 3- or 4- morpholinyl, and Ar may be substituted up to twice with F, Cl, Br, OH, CF3, NO2, CN, OCF3, O-C1-C6 alkyl, (C1-alkyl) -C6), COOH, NH2, (CH2) -phenyl, where n = 0-3; X (C1-C6) alkyl, (CH2) -phenyl, where n can be = 0-6; and the phenyl radical may be substituted, up to twice, with F, Cl, Br, CF3, CN, OCF3, O-C1-C6 alkyl, S-C1-C6 alkyl, C1-C8 alkyl, cycloalkyl (C3-C6), COOalkyl (C1-C8), COOcycloalkyl (C3-C6), CONH2, CONHalkyl (C1-C8), CON [(C1-C6) alkyl] 2; R3 NR10R11, piperazine; R10, R11, independently of each other, H, (C1-C6) alkyl, (C3-C6) cycloalkyl, CO (C1-C6) alkyl, (C1-C6) alkyl -CO-(C1-C6) alkyl, SO2-benzyl-OCH3, (CH2) n-Ar, where n can be = 0-6 and Ar can be equal to phenyl or thienyl; as well as its physiologically compatible salts.
priorityDate 1999-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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