A process for the purification of roxithromycin with high level of impurity -H comprising subjecting the impure roxithromycin to at least partial dissolution and/or suspension in solvent selected from ethanol, acetonitirle, aromatic solvents and mixture of ethanol and acetonitrile; followed by crystallizing to thereby obtain roxithromycin with desired level of impurity-H of less than 0.5%. The invention also relates to crystalline polymorphic forms B and C of roxithromycin obtained following the above process of purification and having impurity-H of less than 0.5%.
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Page 5
(2008/06/13)
Process for preparing erythromycin derivative, such as roxithromycin, from the corresponding oxime
A process for preparing an erythromycin derivative, such as roxithromycin, from the corresponding oxime is disclosed. The oxime is reacted with a metal alkoxide and results in improvements over prior art processes involving the oxime. Roxithromycin is a known anti-bacterial agent.
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(2008/06/13)
Process for preparing roxithromycin and derivatives thereof
A process for preparing an erythromycin derivative of formula (1), such as roxithromycin, from the corresponding oxime is discloded. The oxime is reacted with a metal alkoxide and results in improvements over prior art processes involving the oxime. Roxithromycin is a known anti-bacterial agent.
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(2008/06/13)
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