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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-22
filingDate 1999-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_691970debcc2cc0b7a4d2f00b06d49f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_faf5afc0ee687fa579bd5dfe2d996976
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ca612215132f0bafd04c1cec70996d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a41bb15aa1bbfd531c66207a85c2d947
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8a57c896443b22d4ba714d286df6ffb
publicationDate 2001-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20010029024-A
titleOfInvention Novel isoxazole piperazine derivatives and preparation thereof
abstract The present invention relates to a novel isoxazole piperazine derivative and a method for preparing the same, wherein the isoxazole piperazine derivative acts as an antagonist of the dopamine-1 receptor associated with various central nervous system disorders, and its structure is represented by Chemical Formula 1 Same asn n n n n n n n n n n n n n n R 1 -R 5 in Formula 1 are each independently hydrogen, alkyl, alkoxy, halogen, hydroxy, hydroxymethyl, aryl, heteroaryl, amino, alkylamino, alkenyl, carbonyl, cycloalkyl, heterocyclic group R 6 is hydrogen, alkyl, alkoxy, halogen, aryl, pyridyl group, heterocyclic group or pyrimidyl group, X is nitrogen or carbon, n is 1-4; Q is isoxazole (A) or 4,5-dihydroisoxazole (B) derivative, n has 1-4.n n n The production method is a condensation reaction between amine and aldehyde, and is the same as in Scheme 1.
priorityDate 1999-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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