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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-20
filingDate 1968-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcf33aa20d3a376818206148b2027c4b
publicationDate 1971-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-506558-A
titleOfInvention Process for the preparation of cephalosporin antibiotics
abstract Salts of cephalosporin antibiotics of general formula I with the following amines II: trans-1,3-cyclohexanediamines (A) and their 1,4-analogues (B); trans-1,3-cyclohexane-bis-alkyleneamines (C) and their 1,4-analogues (D) in which the alkylene has up to 3C atoms; 1,3-xylene-alpha,alpha'-diamines (E) and their 1,4-analogues (F). where R = 2-thienylmethyl, 2-furylmethyl, phenylmercaptomethyl, benzyl, nitrobenzyl or CF3-phenyl-mercaptomethyl. and R' = acetoxy (cephalosporanic acid) or H (desacetoxy-cephalosporanic acid). Antibiotics of high and prolonged activity i.e. depot forms resulting from the low solubility in water. The usual Na etc. salts are soluble and when injected parenterally are assimilated and excreted in L hrs. so that 4 injections per day are required.
priorityDate 1968-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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