http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103497228-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-056 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H5-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-056 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7056 |
| filingDate | 2009-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103497228-B |
| titleOfInvention | The synthesis of galactoside inhibitor |
| abstract | The present invention relates to the sulfur synthesis path for digalactosyl glycosides for preparation with formula (12).The method includes using a kind of 3 azido galactosyl thiocarbamide salt derivants, it is corresponding original position mercaptan by this 3 azido galactosyl thiocarbamide salt derivant activation, this mercaptan is made directly to react with a kind of 3 azido galactosyl bromides successively, before this mercaptan has an opportunity to reduce this azido 10, creating 3,3' diazido sulfur is for digalactosyl glycosides.Therefore, 3 azido galactosyl mercaptan are important from being formed in situ synthesis step of this thiocarbamide salt, because any other method producing this mercaptan dividually result in the reduction of the most undesired azide. |
| priorityDate | 2008-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 78.