http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-0144833-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-84
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
filingDate 1993-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81084d5c9f698d348a4a00dc7f59552e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0d5e135d36de051a331db8271aac24b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64bb69b4f12fa06850a3cf8b96ab6ab6
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52f9439054f8b5199aff01d470fbc8c1
publicationDate 1998-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-0144833-B1
titleOfInvention Novel quinazoline derivatives and preparation methods thereof
abstract The present invention relates to a quinazoline derivative, and more particularly to a novel quinazoline derivative represented by the following general formula (I) excellent in gastric acid secretion inhibitory effect, or a pharmaceutically acceptable salt thereof, and a method for preparing the same.n n n n n n n n In formula (I), R 1 , R 2 are hydrogen or C 1-3 alkyl, R 3 is hydrogen or halogen, R 4 , R 5 , R 6 , R 7 , R 8 , R 9 are the same as each other. Or different, hydrogen C 1-3 alkyl, cyclopropyl, or R 5 and R 6 may be taken together to form a cyclopentyl, where R 10 is hydrogen, C 1-3 alkoxy, hydroxy C 1-3 Alkoxy or methylthiomethyloxy.
priorityDate 1992-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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