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filingDate 2004-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d5e5f6d96608f111958c7e6986694a8
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publicationDate 2006-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-RE39383-E
titleOfInvention Process for 6-O-alkylation of erythromycin derivatives
abstract A procedure for preparing 6-O-alkyl erythromycin compounds having the formula: n n nwherein R 1 is a loweralkyl group, R 2 and R 3 an independently hydrogen or a hydroxy-protecting group, except that R 2 and R 3 may not both be hydrogen simultaneously; Y is oxygen or a specifically substituted oxime; and Z is hydrogen, hydroxy or protected-hydroxy; by reaction of the compound wherein R 1 is hydrogen with an alkylating reagent, is the presence of a strong alkali metal base and also in the presence of a weak organic amino base, in a suitable stirred or agitated polar aprotic solvent, or a mixture of such polar aprotic solvents maintained at a reaction temperature and for a period of time sufficient to effect alkyation.
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