http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-421880-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ae6452b86f87f19ee72ca1e7fad35f37 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K- http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C- |
filingDate | 1973-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1976-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-421880-A1 |
titleOfInvention | PROCEDURE FOR OBTAINING PHARMACOLOGICALLY ACTIVE 1-THYMOXI-2-PROPANOL-AMINES. |
abstract | PROCEDURE FOR OBTAINING PHARMACOLOGICALLY ACTIVE 1-THYMOXI-2-PROPANOL AMINES OF GENERAL FORMULA: ** FORMULA ** IN WHICH R1 AND R2 MAY BE DIFFERENT TYPES OF RADICALS. IN THE FIRST PHASE, THYMOL, REACTING WITH ALCOHOLIC OR AQUEOUS NAOH, PRODUCES ITS SODIUM SALT WHICH, TREATED WITH EPICHLORHYDRINE, AT A TEMPERATURE BETWEEN -6 AND 60 DEGREES C FOR 10-18 HOURS AND AFTER EXTRACTING WITH CHLOROFORM, ACIDING, ELIMINATING WITH ACH, LAVING THE CHLOROFORM AND DISTILLING THE RESIDUE IN VACUUM PRODUCES 1-THYMOXY-2,3-EPOXYPROPANE. IN THE SECOND PHASE, THE AMINE CORRESPONDING TO EACH CASE IS ADDED ON THE GLYCIDYL-ETHER ASI OBTAINED DISSOLVED IN ETHANOL, METHANOL OR TETRAHYDROFURANE. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0764640-A1 |
priorityDate | 1973-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.