http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-450207-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7b4beef0c137d9094e6918ee382be22f |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-50 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K- http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D- http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-44 |
| filingDate | 1976-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1977-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-450207-A1 |
| titleOfInvention | A PROCEDURE FOR THE PREPARATION OF NEW SALTS OF 4,5-DIHIDRO-2-ALCOXICARBONIL-AMINO-4-ARIL-IMIDAZOLES. |
| abstract | A procedure for the preparation of new pharmaceutically acceptable 4,5-dihydro-2-alkoxycarbonylamino-4-aryl-imidazoles salts of the formula: **(See formula)** where R is lower alkyl; R1 or R2 is hydrogen, hydroxy, lower alkyl, lower alkoxy, fluorine, chlorine, bromine, iodine or trifluoromethyl and the other is hydrogen, or the same group as the other of R1 or R2 and where R1 and R2 can be in any different position on the phenyl ring, or R1 and R2 together form the methylenedioxy group and are on adjacent carbon atoms in the phenyl ring, characterized in that procedure because it consists in reacting a compound represented by said formula (I) with an organic acid or pharmaceutically acceptable inorganic hydrogen anion to form said pharmaceutically acceptable hydrogen ion addition salt. (Machine-translation by Google Translate, not legally binding) |
| priorityDate | 1975-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 31.