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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C41-26
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-30
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-64
filingDate 2018-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108586273-B
titleOfInvention Preparation method of propranolol hydrochloride
abstract The invention belongs to the field of pharmaceutical chemicals, and particularly relates to a preparation method of propranolol hydrochloride, which comprises the following steps: step 1: reacting 1-naphthol with 1, 3-dibromo (iodo) acetone in sodium hydroxide solution to generate 1-bromo (iodo) -3- (1-naphthoxy) -2-acetone; step 2: reducing 1-bromo (iodo) -3- (1-naphthoxy) -2-propanone with sodium borohydride in an organic solvent to produce 1-bromo (iodo) -3- (1-naphthoxy) -2-propanol; and step 3: reacting 1-bromo (iodo) -3- (1-naphthoxy) -2-propanol with isopropylamine in an organic solvent to produce 1-isopropylamino-3- (1-naphthoxy) -2-propanol; and 4, step 4: the method avoids the use of epoxy chloropropane, is safer and more environment-friendly, does not have an intermediate containing an ethylene oxide structure in the reaction process, and has higher medication safety.
priorityDate 2018-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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