http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7342019-B2

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filingDate 2002-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c0c5cda19fe77fa49f38c011fcdc3ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68bc183111d656c665804bcc83e1c181
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7bdc2a192e0841384ac28bb83f5576ea
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_caf5e54f7531cdf5a52fd9b2db910ee0
publicationDate 2008-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7342019-B2
titleOfInvention 5, 6-diaryl-pyrazine-2-amide derivatives as CB1 antagonists
abstract The present invention relates to compounds of formula (I), and pharmaceutically acceptable salts, prodrugs, solvates and crystalline forms thereof, in which R 1 and R 2 independently represent: a C 1-6 alkyl group; an optionally substituted (amino)C 1-4 alkyl-group; an optionally substituted non-aromatic C 3-15 carbocyclic group; a (C 3-12 cycloalkyl)C 1-3 alkyl-group; a group —(CH 2 ) r (phenyl) s in which r is 0, 1, 2, 3 or 4, s is 1 when r is 0 otherwise s is 1 or 2 and the phenyl groups are optionally independently substituted by Z; naphthyl; anthracenyl; an optionally substituted saturated 5 to 8 membered heterocyclic group containing one nitrogen and optionally one of the following: oxygen, sulphur or an additional nitrogen; 1-adamantylmethyl; a group —(CH 2 ) t Het in which t is 0, 1, 2, 3 or 4, and the alkylene chain is optionally substituted and Het represents an optionally substituted aromatic heterocycle; or R 1 represents H and R 2 is as defined above; or R 1 and R 2 together with the nitrogen atom to which they are attached represent a saturated optionally substituted 5 to 8 membered heterocyclic group as defined above; X is CO or SO 2 ; Y is absent or represents NH optionally substitututed by a C 1-3 alkyl group; R 3 and R 4 independently represent phenyl, thienyl or pyridyl substituted by Z; Z represents a C 1-3 alkyl group, a C 1-3 alkoxy group, hydroxy, halo, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, trifluoromethylsulphonyl, nitro, amino, mono or di C 1-3 alkylamino, mono or di C 1-3 alkylamido, C 1-3 alkylsulphonyl, C 1-3 alkoxycarbonyl, carboxy, cyano, carbamoyl, mono or di C 1-3 alkyl carbamoyl, sulphamoyl and acetyl; and R 5 is H, a C 1-3 alkyl group, a C 1-3 alkoxymethyl group, trifluoromethyl, a hydroxyC 1-3 alkyl group, C 1-3 alkoxycarbonyl, carboxy, cyano, carbamoyl, mono or di C 1-3 alkylcarbamoyl, acetyl, or hydrazinocarbonyl of formula —CONHNR a R b ; with the provisos; and processes for preparing such compounds, their use in the treatment of obesity, psychiatric and neurological disorders, to methods for their therapeutic use and to pharmaceutical compositions containing them.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007099923-A1
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priorityDate 2001-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID230388295
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID244400819
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17824068
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245482511
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223814194
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394313
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23202903
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Total number of triples: 332.