http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02256695-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_56666880a5e2b7703e98a4f9b2d9daf6 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-167 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D279-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-30 |
| filingDate | 1989-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4a4ab20406e39464c1a6897db60790b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9acb9a09fe3e69437c4df6ed7368d16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b813c89e3d445d838e9f01d1373b66e1 |
| publicationDate | 1990-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H02256695-A |
| titleOfInvention | Production on novel r and s diastereomers of adenosine compound |
| abstract | PURPOSE: To obtain the titled compound which inhibits resin production through oral administration and exerts sedative effects and decreased central nervous system depressant effects, by subjecting a compound formed through amination of a specific compound for further reaction. n CONSTITUTION: Chloromethyloxirane is allowed to react with 1-naphthol to obtain a compound of formula I. A compound of formula II, obtained by aminating the compound of formula I, is allowed to react with a compound of formula III in ethanol while being refluxed under heating, to obtain a 1- amino-3-(1-naphthalenyloxy)-2S-propanol of formula IV. The objective N 6 -[2S- hydroxy-3-(1-naphthalenyloxy)propyl] adenosine of formula VI is obtained by allowing the compound of formula IV to react with a compound of formula V. Here, R diastereomer of formula VII is obtained by allowing the compound of formula II to react with the compound of formula III in isopropanol. n COPYRIGHT: (C)1990,JPO |
| priorityDate | 1988-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 41.