http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107382854-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N30-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-56
filingDate 2017-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107382854-B
titleOfInvention Preparation method of high-purity moxifloxacin hydrochloride impurity I
abstract The invention discloses a preparation method of high-purity moxifloxacin hydrochloride photodegradation impurity I, which comprises the following steps: 1-cyclopropyl-6, 7-difluoro-8-methoxy-1, 4-dihydro-4-oxo-3-quinoline carboxylic acid or ester thereof is used as an initial raw material, and moxifloxacin hydrochloride impurity I is obtained through boric acid ester forming reaction, azide reaction, hydrolysis reaction and reduction reaction; the impurity I obtained by the method has high purity and high yield.
priorityDate 2017-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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