http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8503003-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6b460b6e95e64228f98a7ffc6bde16de |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-46 |
| filingDate | 1983-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1985-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-8503003-A1 |
| titleOfInvention | PROCEDURE FOR PREPARING THE 1-ETHOXYCARBONYLOXYETHYLLIC ESTER OF THE 6- (D - (-) - -AMIN- -PHENYLACETAMIDE) PENICILANIC ACID. |
| abstract | PROCEDURE FOR PREPARING THE 1-ETOXICARBONYLOXYETHYL ACID ESTER OF 6- (D - (-) - BAB-PHENYLACETAMIDE) PENICILANIC ACID, CONSISTS OF: A) REACTING AMPICILIN IN THE FORM OF ALKALINE SALT WITH A REACTIVE DYNAMIC ACIDAL ACIDAL APROYCAL REACTIVE DERIVATIVE ALREADY AT A TEMPERATURE BETWEEN 0 AND 60JC AND DURING 2 TO 8 HOURS TO FORM FORMULA ENAMINE (II); B) REACT THE RESULTING INTERMEDIATE WITH BAB-BROMODYETHYL CARBONATE OF FORMULA (III) AT A TEMPERATURE BETWEEN 15 AND 80JC AND DURING 1 TO 24 HOURS TO FORM THE CORRESPONDING ESTER OF FORMULA (IV); AND C) PERFORM A GENTLE HYDROLYSIS IN ACID MEDIA TO OBTAIN THE FORMULA COMPOUND (I). IT HAS THERAPEUTIC PROPERTIES SINCE IT IS WELL ABSORBED, WHEN IT IS SUPPLIED BY ORAL ROUTE, AND GIVES SOME LEVELS OF AMPICILLIN MUCH AMPICILLIN IN THE BLOOD. . |
| priorityDate | 1982-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 22.