http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2209688-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_05a203d85ee01909eaf728dc16f0f6cb |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C39-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-52 |
| filingDate | 1997-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb0dbf1e3bde8cad1170795ddc965f9d |
| publicationDate | 1998-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2209688-A1 |
| titleOfInvention | Preparation of intermediates useful in the synthesis of quinoline antibiotics |
| abstract | Disclosed is a process for producing a compound of the formula (III), by adding a base of the formula (IV) to a solution of a compound of the formula (II) and a halonitromethane of the formula O2NCH2X (where X is halogen) dissolved in a non-aqueous inert solvent. The compound (III) is useful as an intermediate for the synthesis of antibiotic azabicyclo quinoline carboxylic acids (see fig.I) (see fig.II) (see fig.III) (wherein R1 and R3 are each hydrogen, alkyl or aryl or two of R1 form a ring, O is 0-5, m is 0-2, p is 0-3, R2 is alkyl or benzyl and R4 is alkyl). |
| priorityDate | 1996-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 65.