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filingDate 2001-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a38114230ebb34b3f44f08b22f02deda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0304185c428dcc2ff8c578534c7080e9
publicationDate 2008-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2296763-T3
titleOfInvention PIRROLIDINES DISSTITUTED IN 1.3 AS ALFA-2 ADRENORRECEPTOR AMTAGONISTS.
abstract A compound of the formula wherein R0 is hydrogen or (C1-4) alkyl, R1 is (C1-4) alkoxy or (C2-5) alkenyloxy and can also be halogen, hydroxy, (C1-4) alkyl, trifluoromethyl or trifluoromethoxy if A is a group of the formula (c), (e), (f) or (g), and it can also be hydrogen if A is a group of the formula (c), (f) or (g) , R2 is hydrogen, halogen, hydroxy, (C1-4) alkyl, (C1-4) alkoxy, (C2-5) alkenyloxy, trifluoromethyl or trifluoromethoxy, and, when it is in an ortho position with respect to R1, it can also form with R1 a methylenedioxy group, A is tetrahydropyran-4-yl or a group of the formula in which X is O, S or CH = CH, R6 is hydrogen, halogen or (C1-4) alkyl, R7 is hydrogen, alkyl ( C1-6) or cycloalkyl (C3-7) -alkyl (C1-4), R10 is hydrogen, alkyl (C1-4), cycloalkyl (C3-6) -alkyl (C1-4), alkyl (C1-4) -carbonyl, C3-6 cycloalkyl -carbonyl, (C1-4) alkoxy -carbonyl, benzyl, benzyloxycarbonyl, benzoyl, (C1-4) alkyl-sulfonyl, phenylsulfonyl, benzylcarbon yl, benzylsulfonyl, 2-furylcarbonylamino or N-(C1-4) -N- (2-furylcarbonyl) amino, and R11 is hydrogen or (C1-4) alkoxy, in the form of free base or acid addition salt .
priorityDate 2000-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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