http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-247199-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-0222 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-405 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-404 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-113 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-81 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-12 |
| filingDate | 1985-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1994-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1994-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-247199-A1 |
| titleOfInvention | PREPARATION AND OBTAINING OF ACID DERIVATIVES N-ACIL-2,3,3, A, 4,5,7A-HEXAHIDRO ¡1H¿-INDOL-2-CARBOXILICO INTERMEDIARIOS |
| abstract | PREPARATION OF ACID DERIVATIVES N-ACIL-2,3,3A, 4,5,7A-HEXAHIDRO ¡1H¿-INDOL 2-CARBOXILICO, OF FORMULA I, WHERE N IS 0 O 1; R IS HYDROGEN, ALKYL OR PHENYLALKYL MONO-SUBSTITUTED OR NOT WITH METOXI, R1 IS HYDROGEN OR ALKYL MONO SUBSTITUTED OR NOT WITH AMINO, OR EVERY TIME IT MAY BE MONOSUSTITUDED IN POSITION 4 WITH ALCOXY; R2 IS HYDROGEN, ALKYL; AND IT IS HYDROGEN OR HYDROXY; Z IS HYDROGEN; OR Y and Z ARE TOGETHER OXYGEN; YX IS PHENYL MONO-SUBSTITUTED OR NOT IN POSITION 4 WITH ALCOXI, AS WELL AS ITS PHYSIOLOGICALLY SAFE SALTS, WHERE A COMPOUND OF FORMULA IV IS REACTED: WHERE I AND W ARE HYDROGEN OR AN IDENTIAL RAD2 COMPOUND: CH = CH-CO-X AND REDUCE THE SCHIFF BASES OBTAINED AND SEPARATE W BY TREATMENT WITH AN ACID OR A BASE, WITH FORMATION OF FREE CARBOXYL GROUPS; EVENTUALLY REDUCE THE COMPOUNDS OF FORMULA I OBTAINED, WHERE YYZ IS OXYGEN WITH AN ALKALINE BOROHIDRIDE, ALKALINE CYANOBORHYDRIDE IN A ALCOHOL WITH FORMATION OF Y = HYDROXY YZO = YO R IS HYDROGEN, THEY ARE TRANSFORMED IN ESTERS OF FORMULA I, WHERE R IS ALKYL OR PHENYLALKYL BY TREATMENT WITH AN ALCOHOL IN THE PRESENCE OF H2SO4, HC1 OR BF3. |
| priorityDate | 1982-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.