http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100441348-B1

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C50-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D223-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-20
filingDate 2001-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100441348-B1
titleOfInvention A Method for the Preparation of 6-Morphanthridone, the Intermediate of Epinastine
abstract The present invention relates to a novel process for preparing 6-morphantridone, which is an intermediate required for the production of epiastine hydrochloride (Epinastine HC1).n n n Epinastine is 9,13b-dihydro-1H-dibenz [c, f] imidazole [1,5-a] azin-3-amine (9,13b-dihydro-1H-drbenz [c, f] It is the abbreviation for imidazo [1,5-a] azepin-3-amine, and its hydrochloride treats or prevents pain, especially chronic or infection-induced pain, and especially migraines.n n n In the present invention, the anthraquinone of formula (II) is reacted with sodium azide to obtain morphanetridine-6,11-dione of formula (III) to obtain sodium borohydride ( Sodium borohydride) is mixed with trifluoroacetic acid used as a solvent and an activator to prepare 6-morphantridone of Structural Formula (I), which is an intermediate of epinastine hydrochloride. Excluding the use of strong phosgene, anthraquinone of formula (II), which is inexpensive and easy to purchase, can be used as a starting material.
priorityDate 2001-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 40.