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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-236
filingDate 1977-11-14^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-07-03^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d29eaa307eef80bc85f813eeee0bc5e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f354f49f67241fbbb82420ef2cf0e7e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d4b22e199194c01936b86d46d2928bd
publicationDate 1979-07-03^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4160082-A
titleOfInvention Intermediates for aminoglycoside antibiotics
abstract Derivatives of kanamycin A, which have an acyl protecting group on the C-3" and C-6' amino groups, and optionally have a benzyl protecting group on the C-3 amino group, are useful intermediates for the preparation of 1-N-(ω-amino-2-hydroxyalkyl) derivatives of kanamycin A. Derivatives of kanamycin B, which have an acyl protecting group on the C-2', C-3" and C-6' amino groups, and optionally have a benzyl protecting group on the C-3 amino group, are useful intermediates for the preparation of 1-N-(ω-amino-2-hydroxyalkyl) derivatives of kanamycin B. Certain of the partially protected kanamycin A and kanamycin B derivatives of this invention are useful for preparing 1-N-(ω-amino-2-hydroxyalkanoyl) derivatives of kanamycin A and B. 1-N-(ω-Amino-2-hydroxyalkyl) and 1-N-(ω-amino-2-hydroxyalkanoyl)derivatives of kanamycin A and B are known antibacterial agents.
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priorityDate 1976-04-14^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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