http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3781586-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b8e2017b321a8b2a55f4c091d6b89c0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-06
filingDate 2019-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9442bf4a71744fda0e7ad60837bab9d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2fa8bc84d7d67b1a603f16e9b9de9c7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_699fd816b9136a2f8fe4caec21636df6
publicationDate 2021-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3781586-A1
titleOfInvention A method for production of high purity icatibant
abstract The present invention provides a process for the manufacture of peptidomimetic drug icatibant with high yield and purity by fragment condensation on the solid phase. In particular, it describes a convergent synthesis by condensation of a protected C-terminal fragment bound to a solid support and a protected N-terminal fragment, followed by cleavage from the support and resulting in a crude peptide of high purity, which is further purified to obtain pure icatibant in high yield. The invention further provides intermediates useful in the manufacturing process.
priorityDate 2018-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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