http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2352162-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 1999-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32ec3a749520b21283e4e850a015f00b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ecde56022911794e5225a36c6758433
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publicationDate 2000-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2352162-A1
titleOfInvention Novel intermediates, process for preparing macrolide antibiotic agent therefrom
abstract The present invention provides a process for preparing a high yield of purified clarithromycin having broad antimicrobial activity as a macrolide antibiotic agent by using 1,3-benzodithiol-2-ylium tetrafluoroborate (BDFT), which can easily be synthesized from anthranilic acid and used as a protecting group for oxime. In addition, the present invention also provides a process for preparing clarithromycin from 1,3-benzodithiol-2-sulfonic acid group that forms clarithromycin salt which precipitates into crystals in reaction solution thereof, and purifying clarithromycin including a significantly simplified purification step.
priorityDate 1998-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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