http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-608007-A5
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-49 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-49 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-48 |
| filingDate | 1974-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_167dd6207d1b4555e7888eb5268bda3e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8fde1e02a14949d722fb42a3524d89e3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02ed7ef931b827edb520226d00043d45 |
| publicationDate | 1978-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-608007-A5 |
| titleOfInvention | Process for the preparation of novel benzylpyrimidines or their salts |
| abstract | The antibacterially active benzylpyrimidines of the formula adjacent <IMAGE> in which R<1> and R<2> independently of one another denote C1-3-alkyl, C1-3-alkoxy, C2-3-alkenyl or C2-3-alkenyloxy and Z denotes the azido group -N3, and salts of these benzylpyrimidines inhibit bacterial dihydrofolate reductase and potentiate the antibacterial action of sulphonamides. The said compounds are obtained by diazotising corresponding p-aminobenzylpyrimidines and reacting the diazonium compounds thus obtained with sodium azide. If desired, the active compounds formed in this way can then be converted into salts. |
| priorityDate | 1974-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.