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filingDate 1994-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46c9e64a571738b0e464fa438992bfee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8324aae4601288073d36f4f67bfb66bf
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publicationDate 1996-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0712387-A1
titleOfInvention 2-aminoindans as selective dopamine d3 ligands
abstract PCT No. PCT/US94/08046 Sec. 371 Date May 14, 1996 Sec. 102(e) Date May 14, 1996 PCT Filed Jul. 21, 1994 PCT Pub. No. WO95/04713 PCT Pub. Date Feb. 16, 1995Compounds and their pharmaceutically acceptable salts suitable for treating central nervous system disorders associated with the dopamine D3 receptor activity of Formula I: <IMAGE> wherein R1 and R2 are independently chosen from hydrogen, C1-C8 alkyl, OCH3, OH, OSO2CF3, OSO2CH3, SOR5, CO2R5, CONH2, CONR5R6, COR5, CN, SO2NH2, SO2NR5R6, SO2R5, -OCO-(C1-C6 alkyl), -NCO-(C1-C6 alkyl), -CH2O-(C1-C6 alkyl), -CH2OH, -CO-Aryl, -NHSO2-Aryl, -NHSO2-(C1-C6 alkyl), phthalimide, thiophenyl, pyrrol, pyrrolinyl, oxazolyl, or R1 and R2 together form -O(CH2)1-2O- or -(CH2)3-6- (except that only one of R1 and R2 can be hydrogen or OH in any such compound); R3 and R4 are independently chosen from C2-C4 alkenyl, C3-C8 alkynyl, C3-C8 cycloalkyl, -(CH2)p- thienyl (where p is 1-4), or C1-C8 alkyl (except where R1 or R2 are hydrogen or OH or where both R1 and R2 are OCH3 or a C1-C8 alkyl); R5 is hydrogen, C1-C8 alkyl, C2-C4 alkenyl, C3-C8 cycloalkyl; and R6 is C1-C8 alkyl, C2-C4 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, or Aryl.
priorityDate 1993-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 512.