http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-355003-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e5edd48190cba3fa70dd3975efd9831 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-135 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-108 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-135 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-108 |
| filingDate | 1968-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1970-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-355003-A2 |
| titleOfInvention | PROCEDURE FOR THE PREPARATION OF NEW AMINO-KETONES. |
| abstract | Improvements introduced in the object of the main patent No. 354,961, applied for on June 12, 1968 by: a process for the preparation of new amino ketones of the general formula I: **(See formula)** wherein the Hal radicals signify a chlorine or bromine atom; R1 signifies a hydrogen, chlorine or bromine atom; R2 and R3, may be the same or different, signify hydrogen atoms, straight or branched chain alcohol radicals, alkenyl, alkynyl, hydroxy alcohol, alkoxyalkoyl, dialkoxylaminoalcohyl, cycloalkoxy, phenyl, benzyl, or adamantyl or, together with the nitrogen atom, a pyrrolidino, piperidino, hexamethyleneimino, piperazino, morpholino or canfidino ring optionally substituted by lower alcohol radicals or by phenyl radicals; R4 and R5 which may be the same or different, signify hydrogen atoms, alcohol radicals with 1 to 3 carbon atoms or phenyl groups; and n means the numbers 0 or 1 or 2, as well as their acid addition salts physiologically compatible with organic or inorganic acids, characterized in that an amino-halogen-phenyl-amino alkanol of the general formula II is oxidized by means of oxidizing agents. **(See formula)** in which the radicals hal, R1 to R5 and n have the meanings indicated initially and, provided that the compounds obtained are in the form of their salts by addition of acid, they are transformed into their bases if desired, and/or converted to the free bases according to the usual methods in acid addition salts physiologically compatible with an inorganic organic acid. (Machine-translation by Google Translate, not legally binding) |
| priorityDate | 1967-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 26.