http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-183579-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_69c91bbf0395db010b4806f50d808c4e
filingDate 1981-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a207a665fee541ceddbda684becc4a3d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d288dcfc66bd0b5da3830ac231832f3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea6ada2ba4eb9b5f730cafd2af74b488
publicationDate 1984-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-183579-B
titleOfInvention Process for producing l-arginyl-l-lizyl-l-asparagyl-l-valyl-l-tirosine pentapeptide
abstract The present invention relates to a novel process for the preparation of L-arginyl-L-lysyl-L-aspartyl-L-valyl-L-tyrosine pentapeptide (TP-5) by stepwise chain extension in solution, in which the L-valine, L, in each coupling step is used. as the amino-terminal protecting group for aspartic acid and L-lysine, a benzyloxycarbonyl group, a t-butyloxy group for the protection of the L-aspartic acid / 1-carboxyl group, an ω-amino group of the L-lysine, and an amino-terminal protecting group for the last coupling step in L-arginine. and the tert-butyloxycarbonyl group is used and the amino-terminal protecting group is removed by catalytic hydrogenation, with the exception of the last step, after each coupling step, and after the final coupling step, all the protecting groups present are removed by treatment with trifluoroacetic acid. In this way, a very pure product is obtained without any harmful reaction. -1-
priorityDate 1981-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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