http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-617702-A5

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-24
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-24
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-54
filingDate 1974-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d70ed672ea3811aa2fc8ac8de93aa03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5df01905e036a842503e9a1e0b79e624
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7afb7fa9cdf5f1664d026cad4b198d87
publicationDate 1980-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-617702-A5
titleOfInvention Process for the preparation of 6- beta -acylamino-6- alpha -methoxy-penam-3-carboxylic acid compounds and 7- beta -acylamino-7- alpha -methoxy-3-cephem-4-carboxylic acid compounds
abstract Penam and cephem compounds aminomethylated in the acylamino side chain, of the formula I <IMAGE> in which X stands for sulphur or oxygen or for ethenylene of the formula -CH=CH-, and in which the group of the formula -S-A- denotes a radical of the formula <IMAGE> in which R1 represents hydrogen, an etherified hydroxy group or a radical of the formula -CH2-R2, in which R2 denotes hydrogen, a free, etherified or esterified hydroxy or mercapto group or a quaternary ammonium group, and R represents hydroxyl or, together with the carbonyl group -C(=O)-, a protected carboxyl group, are obtained by aminomethylation of compounds of the formula VI <IMAGE> The compounds of the formula I are antibacterial antibiotics.
priorityDate 1974-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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