http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2069724-C

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-113
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575
filingDate 1992-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_164781a25212c06c8d4240dc31bf9766
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_088fa2e87d411f688ba194514454244b
publicationDate 2003-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2069724-C
titleOfInvention Process for making peptides containing aza-amino acids
abstract A process for the solid phase synthesis of peptides containing a C-terminal aza-amino acid, for example the decapeptide goserelin, which comprises: (i) reacting an active ester or imidazolide of an N-protected aza-amino acid either with an appropriate reactive solid support in the case of the synthesis of a peptide containing a C-terminal aza-amino acid, or with a peptide which is attached to a solid support in the case of the synthesis of a peptide containing a non-C-terminal aza-amino acid; (ii) carrying out further conventional solid phase peptide synthesis steps to add sequentially further amino acids, to form a peptide with the required amino acid sequence bound to the solid support; (iii) cleaving the peptide from the solid support, and optionally (iv) reacting the product so formed with hydrazine to remove any acyl groups which have been formed on serine, arginine, tyrosine, threonine or hydroxyproline during the synthesis.
priorityDate 1991-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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