http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-880992-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-234
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-234
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-00
filingDate 1959-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1961-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-880992-A
titleOfInvention Compounds of kanamycin and tetracycline type antibiotic
abstract Compounds of kanamycin and a tetracycline are produced by reacting 1 mol of kanamycin with one to four moles of (a) formaldehyde or a polymer thereof and (b) one to four mols of tetracycline, 5-oxytetracycline, 7-chlorotetracycline, anhydrotetracycline, 7-bromotetracycline, 6-deoxytetracycline or 6-demethyldeoxytetracycline. The compounds are prepared by adding an aqueous solution of kanamycin to a solution of the tetracycline and formaldehyde in a water-miscible organic solvent such as methanol or ethylene glycol monomethyl ether. The kanamycin may be kanamycin A or B, a naturally produced mixture of A and B or a prepared mixture of A and B. The compounds are monoditri- or tetra- N1-tetracyclylmethyl kanamycins wherein, in the case of tetracycline, the N1-tetracyclylmethyl radical has the formula <FORM:0880992/IV (b)/1> a kanamycin molecule being bound to one to four tetracycline molecules through one to four methylene groups, which are attached both to the nitrogen atom of a primary amino group of kanamycin and to the nitrogen atom of the carboxamido group of the tetracycline. The non-toxic acid addition salts may be prepared from these compounds by conventional means. Specification 817,385 is referred to.
priorityDate 1958-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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