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publicationDate 2014-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2014012668-A
titleOfInvention Macrolide synthesis method
abstract An object of the present invention is to provide a cost-effective method for producing a macrolide with a high yield and a treatment method using the macrolide. Tylosin A (or a salt thereof) is reacted with a specific piperidinyl compound and formic acid to form a 20-piperidinyl-tylosin compound, then reacted with an acid, further reacted with an acid, and 23 Forming a hydroxy-20-piperidinyl-5-O-mycaminosyl-tylonolide compound and further forming an activated compound with an activator, or reacting the activated compound again with a piperidinyl compound, or a macrolide thereof Method for producing salt. An animal in need of producing the macrolide or a pharmaceutically acceptable salt thereof and treating a disease selected from the group consisting of pasteurellosis, porcine respiratory disease and bovine respiratory disease with a therapeutically effective amount of the macrolide or salt. A method for treating the disease, comprising administering to the disease. [Selection figure] None
priorityDate 2006-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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