http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2523463-C1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ff346a4b8595551f1fdd6153af5a1907 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-155 |
| filingDate | 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a9b8eb289a3e2c64310fb30996902b4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d516dd9d911781b4fe427110098d55e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_839d5bef9dbd58653ec6e35fc3ad0b0e |
| publicationDate | 2014-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2523463-C1 |
| titleOfInvention | Method of 2-amino-2-cyanoadamantane transamination |
| abstract | FIELD: chemistry. n SUBSTANCE: method consists in an interaction of α-aminonitrile with amines with heating. As α-aminonitrile, 2-amino-2-cyanoadamantane is used, and as amines - cyclohexylamine, 3-aminopropanol and morpholine. The process is carried out in the presence of potassium carbonate at 80-100°C. n EFFECT: method makes it possible to increase the output of 2-amino-2-cyanoadamantane derivatives. n 3 ex |
| priorityDate | 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.