http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8306369-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8c646f75c4f7c6349f35c8fe01934921
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-38
filingDate 1982-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1983-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8306369-A1
titleOfInvention "A PROCEDURE FOR THE PREPARATION OF 2-TENOILMERCAPTOPROPIONYLGLYCIN ESTERS".
abstract PROCEDURE FOR THE PREPARATION OF ESTERS OF 2-TENOYLMERCAPTOPROPIONYLGYCIN, OF GENERAL FORMULA (I), IN WHICH R IS A RADICAL CHOSEN BETWEEN P-ACETAMIDOBENZYL, P-PROPYLOXICARBONYL AND O-ALKYLOXYL OXYCARDONYL OF SETIENOXICARBONYL FROM 1 TO 4 CARBON ATOMS AND IS, OF PREFERENCE, METOXYL OR ETOXYL. IT CONSISTS OF REACTING 2-TENOYLMERCAPTOPROPIONYLGLYCIN WITH A CHLOROFORMATE OF FORMULA: CLCOOR, WHERE R IS ALKYL WITH 1 TO 4 CARBON ATOMS, TO OBTAIN A MIXED ANHYDRIDE. THE MIXED ANHYDRIDE OBTAINED IN THE PREVIOUS REACTION IS REACTED WITH A SUBSTITUTED HYDROXYBENZENE CHOSEN FROM P-HYDROXYBENZEN-ACETAMIDE, PROPYL P-HYDROXYBENZOATE AND ALKYBENZO O-HYDROXYBENZOATE. OF APPLICATION IN PHARMACEUTICAL PREPARATIONS FOR ITS MUCOLYTIC AND ANTI-INFLAMMATORY ACTIVITY.
priorityDate 1981-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 23.