http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-291558-A5

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ce010dfc8c8ee1224db9be853afeb081
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1990-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a439bb5f2e45851466cfd7c74559cd83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4040c4d24e33b9888b9fc6bf9072ef36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc1ce520d8eb120b331e6cbf6174caa0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_045d2e408244bd4fdb8e1325916547be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47d53e71608599d7fca114a28bff8720
publicationDate 1991-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-291558-A5
titleOfInvention PROCESS FOR PREPARING A NEW 1,8-BENZONAPHTHYRIDINE DERIVATIVE
abstract The invention relates to processes for preparing novel 1,8-benzo / b / naphthyridine derivatives of the general formula (I) (see formula sheet), wherein R is a hydrogen atom, an alkyl radical, a fluoroalkyl radical, a cycloalkyl radical having 3 to 6 carbon atoms, an alkyloxy radical, an alkylamino radical or an amino-protecting group, and either Hal is a fluorine, chlorine or bromine atom and R is a hydrogen atom, or the symbols Hal and R are simultaneously fluorine atoms and their salts , These new products are useful as local antimicrobial agents or as synthesis intermediates. {1,8-benzo / b / naphthyridine derivatives preparation; Pharmaceuticals, antimicrobial}
priorityDate 1989-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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