| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dfae81468523c4a7e635145a1bfe2359 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D453-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C215-66 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-137
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D453-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B55-00 |
| filingDate |
2000-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2002-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a4b147ac50c366b872a5145542719a1 |
| publicationDate |
2002-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
DE-10028443-C1 |
| titleOfInvention |
Process for the preparation of 3,3-diarylpropylamines, (R, S) - and (R) -4-phenyl-2-chromanone-6-carboxylic acid and (R) -4-phenyl-2-chromanone-carboxylic acid cinchonidine salt and their Use for the preparation of a clockwise hydroxybenzyl alcohol and pharmaceutical compositions |
| abstract |
The invention relates to a process for the preparation of derivatives of 3,3-diarylpropylamines of the general formula I DOLLAR F1 and sterically highly pure, stable intermediates and their use for the production of pharmaceutical compositions. DOLLAR A The process according to the invention comprises only 6 process steps for obtaining a compound of formula I in which the necessary resolution is already carried out in stage 1 of the process. DOLLAR A Finally, the enantiomer of a compound of the formula II which is clockwise rotating as the free base is obtainable according to the invention. DOLLAR F2 |
| priorityDate |
2000-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |