http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2016145301-A1

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filingDate 2015-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf268765e10b3d0d17642060c356f5bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_910ceb9d94cdf696a7cf06d323ebb9d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e3e10826bd4a69a8302c1a07c32f6cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_347ed6ecb6359cb2f933e75ba030266a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d808267833e1133c23b8d02af9cb1a7
publicationDate 2016-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2016145301-A1
titleOfInvention Process for the manufacture of degarelix and its intermediates
abstract The present invention relates to a liquid (or solution)-phase manufacturing process for preparing the decapeptide Degarelix, its protected precursor, and other useful intermediates. The invention further relates to polypeptides useful in the solution-phase manufacturing process and to the purification of Degarelix itself. Degarelix can be obtained by subjecting a Degarelix precursor according to formula II: (P 1 )AA 1 -AA 2 -AA 3 -AA 4 (P 4 )-AA 5 -AA 6 (P 6 )-AA 7 -AA 8 (P 8 )-AA 9 -AA 10 -NH 2 (II) or a salt or solvate thereof, to a treatment with a cleaving agent in an organic solvent, wherein P 1 is an amino protecting groups; preferably acetyl; P 4 is hydrogen or a hydroxyl protecting group, preferably a hydroxyl protecting group; P 6 is hydrogen or an amino protecting groups; preferably an amino protecting groups; and P 8 is an amino protecting group.
priorityDate 2010-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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