http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100248558-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-18
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-30
filingDate 1992-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa542edc0575f82b53de82870859a9b8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b16241b7228ab1f5cd842617bb0ad83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9ee2d59cb15e2b05f4afc58988620bd
publicationDate 2000-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100248558-B1
titleOfInvention Substituted tetrahydroisoquinoline, preparation method thereof and pharmaceutical composition comprising the same
abstract FIELD OF THE INVENTION The present invention relates to tetrahydroisoquinoline compounds of formula (I), pharmaceutically acceptable salts thereof and O-acylated derivatives thereof, wherein the anesthesia and psychosis (eg schizophrenia), Parkinson's disease, Lesh-Nian syndrome And lipophilic esters useful for the treatment of intensive deficiency or cognitive impairment or for the alleviation of drug dependent or delayed dyskinesia.n n n n n n n n Wheren n n R is H, halo, hydroxy, alkyl having 1 to 3 carbon atoms (optionally substituted by hydroxy), alkoxy having 1 to 3 carbon atoms, alkylthio having 1 to 3 carbon atoms, alkylsulfinyl having 1 to 3 carbon atoms Selected from 1 to 3 alkylsulfonyl, nitro, cyano, polyhaloalkyl of 1 to 3 carbon atoms (optionally substituted by one or more substituents selected from alkyl of 1 to 3 carbon atoms and alkoxy of 1 to 3 carbon atoms) Carbamoyl optionally alkylated by one or more or one or two alkyl groups of 1 to 3 carbon atoms,n n n R 2 is an aliphatic group having 1 to 3 carbon atoms optionally substituted by alkoxy or hydroxy having 1 to 3 carbon atoms,n n n E is an alkylene chain of 2 to 6 carbon atoms optionally substituted with 1 to 3 carbon atoms and at least one alkyl group,n n n G may be phenyl or the same or different, and is independently alkyl having 1 to 3 carbon atoms, alkoxy having 1 to 3 carbon atoms, halo, hydroxy, polyhaloalkyl having 1 to 3 carbon atoms, polyhalo having 1 to 3 carbon atoms. Alkoxy, cyano, alkylthio having 1 to 3 carbon atoms, alkylsulfinyl having 1 to 3 carbon atoms, alkylsulfonyl having 1 to 3 carbon atoms, (halo, alkyl having 1 to 3 carbon atoms and alkoxy having 1 to 3 carbon atoms Phenyl optionally substituted by one or more of the above substituents or a phenyl substituted by one or more substituents which are carbamoyl optionally alkylated by one or two alkyl groups of 1 to 3 carbon atoms, or a heterocyclic or aromatic carbocyclic ring fused Phenyl ring.
priorityDate 1991-12-23-04:00^^<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/SID423024020
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413452666
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419747755
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22406773
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419490211
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423024016
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22406772
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID92214
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID64037984
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423024015

Total number of triples: 612.