http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0185220-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-36 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36 |
| filingDate | 1985-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73df70c4e81373ab7f83bc0c3caccba2 |
| publicationDate | 1986-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0185220-A2 |
| titleOfInvention | Intermediates for the preparation of cephalosporins |
| abstract | können durch Behandeln mit einem Gemisch aus Wasser und einem primären C 1-3 -Alkohol und einer anorganischen Base bei einem pH von 6-9 in das antibiotisch wirksame Cephalosporin 7-[2-(2-Amino-4-thiazolyl)-2-syn-hydroxyiminoacetamido] - 3-{[(2,5-dihydro-6-hydroxy-2-methyl-5-oxo-as - 3-triazinyl)thio]methyl}-3-cephem-4-carbonsäure übergeführt werden. The new compounds of the formula where R is lower alkanoyl, can by treating with a mixture of water and a primary C 1-3 alcohol and an inorganic base at a pH of 6-9 in the antibiotic cephalosporin 7- [2- (2-Amino-4-thiazolyl) -2-syn-hydroxyiminoacetamido] - 3 - {[(2,5-dihydro-6-hydroxy-2-methyl-5-oxo-as - 3-triazinyl ) thio] methyl} -3-cephem-4-carboxylic acid. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9620198-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9207840-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006008160-A1 |
| priorityDate | 1984-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 67.