http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050086927-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bdd619b8a2cc2f110b9ee4dc8d896a17 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-56 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-56 |
| filingDate | 2003-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1587b0ec1e887ffea2d4739093956e72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7b6d4b6903adb22899003db67d4bb6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cdf9a75e7b6b4ee6a3a6ea04d076b34d |
| publicationDate | 2005-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20050086927-A |
| titleOfInvention | 1-alkyl-3-aminoindazoles |
| abstract | A method for preparing 1-alkylindazole is described. This method involves reacting 2-alkylaminobenzonitrile with a nitrification agent and subsequently reducing-ringing the resulting nitrosamine to form 1-alkyl-3-aminoindazole. The 1-alkyl-3-aminoindazole can be deamined to form 1-alkylindazole and ultimately 1-alkylindazole can be used to form the desired indazole, which is preferably a pharmaceutically active product. have. The enantiomers, such as aminoalkyl indazoles, can further form rich or pure indazoles by the process of the invention. |
| priorityDate | 2002-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 54.