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filingDate 1998-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571a56049700f9445fe2bc753adf02d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f51205ece3ac1cdc92d1c512faa6d3f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_427556bd36ddf3c314f8888eebb7ef81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0924238925f2d489ab6de51c25dbd740
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_950de802da23d33641f68d1e4492a703
publicationDate 1999-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-9801587-A2
titleOfInvention 5H-Thiazolo [3,2-a] pyrimidine derivatives, process for their preparation, intermediates, use and pharmaceutical compositions containing them
abstract The present invention relates to compounds of general formula (I) (wherein R 1 is hydrogen, alkyl, phenyl or benzyl pt; R 2 is alkyl, alkoxy pt, -O (CH 2) n N (R 13) (R 14) -, - (CH 2) n N (R 13)). (R14) - or -N (R15) (CH2) nN (R13) (R14) -; R3-R12 are hydrogen, halogen, trifluoromethyl, alkyl, cycloalkyl, alkoxy, hydroxy, nitro, cyano, -N (R 13) 2 -, phenyl, phenyloxy, benzyl, or benzyloxy, or R 6 and R 7 together form a benzo ring; R 13 - R 15 are hydrogen, alkyl or cycloalkyl, and n is 1-5; ) and pharmaceutically acceptable salt salts. The present invention relates to a process for the preparation of the compounds, a pharmaceutical composition for use in the treatment of neuro-biological disorders, and a pharmaceutical composition containing them. The compounds of the present invention are antagonists and / or agonists of the metabotropin glutamate receptor. ŕ
priorityDate 1997-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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