http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4338455-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-06 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-06 |
filingDate | 1981-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1982-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6b72fd634103b50b3ce9045008a99c5 |
publicationDate | 1982-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-4338455-A |
titleOfInvention | Novel process and intermediates useful in the preparation of sympathomimetic amines |
abstract | The invention relates to a novel process and novel intermediates useful in the preparation of sympathomimetic amines. The pharmacologically useful final products, which are acyl derivatives of mono- and dihydroxy aromatic amines (e.g., catechol amines) can be prepared in optically active or racemic form by reacting the corresponding mono- or dihydroxy aromatic amine with a reagent capable of forming the N-tert-butoxycarbonyl derivative thereof; reacting the novel intermediate thus obtained with an acyloxymethyl chloride to afford the corresponding novel mono- or diacylated N-protected aromatic amine; and removing the N-protecting group therefrom. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4754047-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4705798-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4968829-A |
priorityDate | 1981-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 417.