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filingDate 1998-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_649fd8f5f0c187f6a2d554d84b1df654
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publicationDate 2000-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20000032351-A
titleOfInvention Method for preparing 6-O-methylerythromycin A type 2
abstract In the present invention, 6-O-methylerythromycin A synthesized from erythromycin A is dissolved in an acid solution or a mixed solvent of an aqueous organic solvent and an acid solution, and the precipitate formed by adding alkali is filtered and dried under reduced pressure at 45-50 ° C. Provided is a method of preparing 6-O-methylerythromycin A Form 2 in high purity and high yield.
priorityDate 1998-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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