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filingDate 2007-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4756e855c0e88dc96f8747ec2888c074
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publicationDate 2007-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NO-20070877-L
titleOfInvention Aryl and heteroaryl substituted tetrahydroisoquinolines and their use to block reuptake of norepinephrine, dopamine and serotonin
abstract The compounds of the present invention are represented by the chemical structure shown in formula (I) wherein: The carbon atom represented by * is in the R or S configuration; and X is a condensed bicyclic carbocycle or heterocycle selected from the group consisting of benzofuranyl, benzo [6] thiophenyl, benzoisothiazolyl, benzoisoxazolyl, indazolyl, indolyl, isoindolyl, indolizinyl, benzoimidazolyl, benzooksazolyl, benzooksazolyl, benzooksazolyl, benzooksazolyl pyridinyl, pyrazolo [1,5-a] pyridinyl, [1,2,4] triazolo [4,3-a] pyridinyl, thieno [2,3-6] pyridinyl, thieno [3,2-b] pyridinyl, 1H -pyrrolo [2,3-b] pyridinyl, indenyl, indanyl, dihydrobenzocycloheptenyl, tetrahydrobenzocycloheptenyl, dihydrobenzothiophenyl, dihydrobenzofuranyl, indolinyl, naphthyl, tetrahydronaphthyl, quinolinyl, isoquinolinyl, 4-isoquinolinyl, 4-isoquinolinyl, 4-isoquinolinyl [1,2,3] triazinyl, benzo [1,2,4] triazinyl, 2H-chromenyl, 4H-chromenyl and a condensed bicyclic carbocycle or condensed bicyclic heterocycle optionally substituted with from 1 to 4 substituents as defined in R14; and wherein R1, R2, R3, R4, R5, R6, R7, R8 and R14 are as defined herein.
priorityDate 2004-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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