http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007084537-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_05a203d85ee01909eaf728dc16f0f6cb |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 |
| filingDate | 2006-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84b109f4067c4ae3b5a42d5413217d30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9b0ac051bc388a4d9fca906648230cc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e35f8e044291a2a0d64a26429c153440 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fde41eba78e958abd4c83d1618ed9c77 |
| publicationDate | 2007-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2007084537-A |
| titleOfInvention | An improved method for preparing benzene-fused heteroarylamide derivatives of thienopyridine |
| abstract | 6-[(imidazol-2-yl) thieno [3,2-b] pyridin-7-yloxy] -1H-indole-3-carboxylic acid amide useful as an anti-angiogenic agent and protein kinase inhibitor Provision of a method for producing a derivative. A compound (V) is obtained by subjecting 7-halo-thieno [3,2-b] pyridine as a starting material to formylation, cyclization reaction, and alkylation reaction. Compound (V) and compound (X) are coupled to obtain the target compound (I) [wherein R 1 , R 2 , R 3 and R 4 each represent H or a C 1 -C 6 alkyl group, Y represents -O-, -S- or -NH-]. [Selection figure] None |
| priorityDate | 2005-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 197.