http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-505122-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-088 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-088 |
| filingDate | 1969-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffa2bcdd6588730775ace40ddfbe0cea http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ea0c8c1d293c4f6786b9787acf729d6 |
| publicationDate | 1971-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-505122-A |
| titleOfInvention | Process for the preparation of new imidazolidinone derivatives |
| abstract | Imidazolidinone derivs.; psychosomatic agents and antiemetics New cmpds. of formula: (where X = H, or Cl; m = 2 or 3; R1 = Me or Et; R2R3 = H or supplementary bond) and their salts are prepd. by reacting either (a) a 3-(benzodiazepin-5-yl)-2-methyl-propylpiperazine (I) with a reactive ester of a 1-(hydroxyalkyl)-2-imidazolidone or (b) a reactive ester of a 3-(benzodiazepin-5-yl)-2-methyl-propanol with a 1-(1-piperazinoyl-alkyl)-2-imidazolidone or (c) a benzodiazepine with a reactive ester of a 1- 4-(3-hydroxy-2-methyl-propyl)-1-piperazinylakyl -2-imidazolido- ne or (d) (I) with an N,N-bis-(haloethyl) urea. |
| priorityDate | 1969-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 121.