http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0002718-A2

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filingDate 1998-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b676917a9402600909892d7dbd9e6eab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_329c3baee60ebedfcc16b7b0f1dd1bec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d073f29336e8dbba9421a34182f95615
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_191e77515b956574975939d99d3ee62b
publicationDate 2001-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0002718-A2
titleOfInvention Piperazine derivatives, process for their preparation and pharmaceutical compositions containing them
abstract The present invention relates to piperazine derivatives of formula (I) wherein R1 is unsubstituted or mono- or di-halogen, CN, A-, AO-, HO-, -CONH2, -CONHA, -CONA2, -COOH, -COOA, -CH2OH, Indol-3-yl substituted with -CH2OA, -CH2NH2, -CH2NHA and / or -CH2NA2, R2 is unsubstituted or mono- or di-halogen, A-, AO-, -OH, CN, -NO2, -NH2, -NHA , -NA2, -COA, -CONH2, -CONAH, -CONA2, -CH2OH, -CH2OA, -CH2NH2, -CH2NHA, -CH2NA2, -COOH and / or -COOA-substituted 2-oxo-2H-1-benzopyran-6 -Il or 2-oxo-2H-1-benzopyran-4-yl, Hal is fluorine, chlorine, bromine, or iodine, A is straight or branched, C 1 -C 10 alkyl having 1 to 5 fluoro- and / or may be substituted with chlorine, or is a C3-C10 cycloalkyl group, to a degree of 2, 3 or 4. The compounds affect the serotoninergic transmission. HE
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7244846-B2
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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