http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-529702-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bba842fc4d37dfcaced1b55bc0c91c7c |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-90 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-90 |
filingDate | 1970-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac2c5070185bb095adb6af81532a504d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8018fcf8bc401f9e0f8de26ad9cf27dc |
publicationDate | 1972-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CH-529702-A |
titleOfInvention | Process for the production of new Benz (cd) indoles |
abstract | Optically active forms of benz (c,d) indoles of formula (I): (where either X is H, halogen, Me or MeS- and Y is H; or X is H and Y is Me; or both X and Y are Cl) and their addn. salts have pharmacodynamic props. They are prepd. by converting the racemates, pref. 1,2,2a,3,4,5-hexahydro-1-(2-imidazolin-2-ylamino)-benz(c,d)-indol- e, with optically active acids, pref. (-)-di-O-p-toluyl-D-tartaric acid into the mixt of their diastereiosmeric salts; sepg. the otpical isomers of (I) and opt. converting salts obtd. to the free bases. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0000151-A1 |
priorityDate | 1970-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 94.