http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108440330-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-46
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-26
filingDate 2018-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108440330-B
titleOfInvention Preparation method of doxycycline hydrochloride
abstract The invention provides a preparation method of doxycycline hydrochloride. The preparation method comprises the following steps: carrying out hydrogenation reaction on 11 a-chloro-6-methenyloxytetracycline p-toluenesulfonate under the conditions of a catalyst and a toxic agent; then, the alpha-6-deoxyoxytetracycline sulfosalicylate is obtained by reaction with sulfosalicylic acid; reacting with a hydrogen chloride-ethanol solution, adding water, stirring and crystallizing to obtain doxycycline hydrochloride; wherein said toxic agents comprise: mixtures of sulfur-containing and nitrogen-containing organics. The method can improve the yield and stereoselectivity of doxycycline hydrochloride and obtain high-quality raw material medicines.
priorityDate 2018-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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