http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FI-854329-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_05a203d85ee01909eaf728dc16f0f6cb |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D- |
| filingDate | 1985-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e50d089bd7d9d32e849fe6005e430878 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8328432714f5e559c04f649e1053f99 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90c9b3e2ba21b6bde6044625a1ed638b |
| publicationDate | 1985-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | FI-854329-A |
| titleOfInvention | FOERFARANDE FOER FRAMSTAELLNING AV NYA TERAPEUTISKT ANVAENDBARA BICYKLISKA BENSOFUSIONERADE FOERENINGAR. |
| abstract | The invention relates to a method for production of new therapeutically useful bicyclic benzofused compounds with formula I, in which formula R2 and R3 each are hydrogen atoms or methyl groups, R1 is hydrogen or CH3CO-, Z is -O- CH(CH3)CH2CH2CH2- or -C(CH3)2(CH2)6-, and W is hydrogen or phenyl. The compounds with formula (I) are produced by reducing a compound with formula (IX) or (X), in which Y1 is hydrogen, methyl, benzyl, benzoyl or acetyl and R7 is hydrogen, methyl or ethyl, in the presence of a reaction- inert solvent by means of a metal hydride, preferably lithium aluminium hydride, or by catalytic hydration with a noble metal catalyst at a temperature of 0-60 degree C. <IMAGE> |
| priorityDate | 1982-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 22.