http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-224425-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c902faf6ae746c51fc8010672fc22894
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-16
filingDate 2000-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f913bdcf0212472ed5418773432f2f66
publicationDate 2005-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-224425-B1
titleOfInvention Heterocyclic intermediates useful in the preparation of (5R) - (Methylamino) -5,6-dihydro-4H-imidazo [4,5,1-ij] quinolin-2 (1H) -one
abstract The present invention relates to pharmaceutically acceptable (5R) - (methylamino) -5,6-dihydro-4H-imidazo [4,5,1-ij] quinolin-2 (1H) -one, i.e. the compound of formula (VII). applies to intermediates that can be used in its new production process. Typical of these are compounds of formula (II): wherein RN is benzyl (A), the phenyl moiety of which is optionally substituted with one or two fluorine, chlorine, bromine or iodine compounds independently selected from alkyl or alkoxy; (B) RN1-CH2-O-CH2-, wherein RN1 is (1) phenyl optionally substituted with fluorine, chlorine, bromine or iodine, or alkyl or alkoxy, (2) (CH3) 3Si-CH2 - (3) RN2-O-CH2-, wherein RN2 is alkyl, (4) CH2 = CH-, (5) hydrogen, (6) alkyl; (C) Unsaturated CH2 = CH-CH2-, CH3-CH = CH-CH2- or phenyl-CH = CH-CH2-.
priorityDate 1999-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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