http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010075994-A1

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filingDate 2009-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66d90b6931faebafa9dfed86ffc10a01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f716ff3a87342943f7589a01de572be
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publicationDate 2010-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2010075994-A1
titleOfInvention Substituted dihydro and tetrahydro oxazolopyrimidinones, preparation and use thereof
abstract The present invention relates to a series of substituted dihydro and tetrahydro oxazolopyrimidinones, specifically, to a series of 2-substituted-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-ones and 2-substituted-2,3,5,6-tetra-hydro-oxazolo[3,2-a]pyrimidin-7-ones of formula (I): n n n n n n n n n n Wherein p, n, X, Y, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined herein. This invention also relates to methods of making these compounds including novel intermediates. The compounds of this invention are modulators of metabotropic glutamate receptors (mGluR), particularly, mGluR2 receptor. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic neurodegenerative conditions, psychoses, convulsions, anxiety, depression, migraine, pain, sleep disorders and emesis.
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priorityDate 2007-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 3103.