http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1458325-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_56ee5285e8e8edccb061046ff20da7a6 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5025 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-14 |
| filingDate | 1975-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1976-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1458325-A |
| titleOfInvention | Nitroimidazolyl-s-triazolo-4,3-b-pyridazines |
| abstract | 1458325 3-[5-Nitro-1-methyl-2-imidazolyl]-striazolo[4,3,-6]-pyridazines BOEHRINGER MANNHEIM GmbH 11 April 1975 [17 April 1974] 15030/75 Heading C2C Novel compounds (I) and their acid addition salts in which Z is methyl, amino or C 1-3 alkylamino are prepared by reacting a compound II with (i) a compound NH = C(Z)-NH 2 when X is halogen or a sulphonyl radical, (ii) a compound A-C(Y)(B)Z in which Y is C 1-6 alkoxy or alkylthio and A and B are alkoxy when X is amino, followed by reaction with ammonia or (iii) a nitrile Z-CN when X is amino, and if desired converting the compound obtained into a salt. Compounds I have anti-microbial activity and form with a carrier or diluent a pharmaceutical composition which may be administered orally or parenterally. |
| priorityDate | 1974-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 16.