http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102417531-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 2011-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5db8c42def2abb6000a82834713f16c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_204043944910a8d3f9cf682ff64af21c
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publicationDate 2014-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102417531-B
titleOfInvention Method for preparing azithromycin monohydrate
abstract The invention mainly discloses a method for preparing an azithromycin monohydrate. The azithromycin monohydrate is prepared by crystallizing an azithromycin dihydrate or 9-deoxo-9a-aza-9a-homoerythromycin A which are taken as raw materials. The method comprises the following steps of: slowly adding the raw materials and water which is taken as an anti-solvent-out agent into an acetone-methanol mixed solvent at proper temperature, crystallizing, filtering, and baking under baking conditions to obtain the stable azithromycin monohydrate in which the residual quantity of the solvent is qualified. The method is easy to operate and high in yield (more than or equal to 95 percent), the quality is high (more than or equal to 98.5 percent), and the obtained product has a good crystal form, is high in fluidity and preparation adaptability, and can be industrially controlled easily.
priorityDate 2011-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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