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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-22
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-34
filingDate 1978-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79482cdbb998e5892c120632db5cf851
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publicationDate 1980-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5540616-A
titleOfInvention Preparation of benzo-hetero-compound
abstract PURPOSE: To prepare the title compound useful as an intermeidate of antibiotic agent, by reducing a 4-dihydrocarbostyril derivative which is a known or an easily synthesizable compound. n CONSTITUTION: A benzo-hetero-compound of formulaII(R 1 is H, OH, amino, halogen, alkoxy, alkyl, alkanesulfonyloxy or allenesulfonyloxy; R 2 is H, halogen, alkoxy, alkyl, or phenylalkoxy; R 3 is H, halogen or alkoxy; l is 1W3), e.g. 5- methanesulfonyl-oxy-1,2,3,4-tetrahydroquinoline, is prepared by reducing a 3,4- dihydrocarbostyril derivative of formulaI, e.g. 5-methanesulfonyloxy-3,4-dihydrocarbostyril, preferably with a hydrogenating agent such as sodium borohydride. n COPYRIGHT: (C)1980,JPO&Japio
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