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filingDate 2004-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70ab57243603efd52e12a1b09be76fe2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9969a4283024e250b579e7a01e63b70
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5f52fb44d6669a636f2c54737eb7180
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d5f0e02488f9442e660e31d020ee1b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7a09322b44a3ccac4bdebef8af3dd0f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86a01ffb377fbb9b73cb8797401fb10b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3046cf42d8e30e659edc9f123dbc9522
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publicationDate 2005-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200529826-A
titleOfInvention Pyrazolyl derivatives, preparation process and intermediates of this process as medicinal products and pharmaceutical compositions containing them
abstract The present invention relates to the novel derivatives of formula (I) in which, A is, if it is present, a (C1-C6) alkyl radical, a (C3-C6) alkenyl radical, a (C3-C6) alkynyl radical, a (C3-C7) cycloalkyl radical or a (C5-C7) cycloalkenyl radical, R1 is an NR6R7, (C4-C7) azacycloalkyl, (C5-C7) azacycloalkenyl, (C5-C9) azabicycloalkyl or (C5-C9) azabicycloalkenyl group; A-R1 is such that the nitrogen of R1 and the nitrogen in the 1-position of the pyrazole are necessarily separated by at least two carbon atoms, R3 is an H, halogen, OH, SH, NH2, Orc, SRc, SORa, SO2Ra, NHCHO, NRaRb, NHC(O)Ra, NHC(S)Ra or NHSO2Ra radical, R4 is an aryl or heteroaryl radical; and R5 is an H, halogen, CF3, CHF2, CH2F, linear or branched (C1-C6) alkyl or (C3-C7) cycloalkyl radical, to their racemates, enantiomers and diastereoisomers and to their mixtures, their tautomers and to their pharmaceutically acceptable salts.
priorityDate 2003-11-25-04:00^^<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: 827.