http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010094011-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e5f3612b46c547b35d51c914fee1336b http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf4981b7083efaa60d98c05beaeb67aa http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b4ae573fb71360ae22f6eebb7e775bdd |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D453-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-416 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-56 |
filingDate | 2009-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b63d2b155efdf3937a785ec302d4450 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75b725a85bfe758f4cb1f4525b37d709 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4be22aa08d3790b993ca43a12abe626 |
publicationDate | 2010-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-2010094011-A1 |
titleOfInvention | Diazonium-free method to make an indazole intermediate in the synthesis of bicyclic 5-(trifluormethoxy)-1h-3-indazolecarboxylic acid amides |
abstract | The present invention provides novel methods for preparing 5-(trifluoromethoxy)-1H-3-indazolecarboxylic acid (3), which is a useful precursor for the preparation of bicyclic-5-trifluoromethoxy-1H-indazole-3-carboxylic acid amides of Formula (1). Compounds of Formula (1) are active as agonists and partial agonists of the nicotinic α-7 receptor and are being studied for their use in the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain, such as for the treatment of Alzheimer's disease and schizophrenia, as well as other psychiatric and neurological disorders. The present methods are useful for preparing compound (3) on scale up levels. |
priorityDate | 2008-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 228.