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filingDate 2018-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb790cdb397d132568a1488efd33aae7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00597932a926cbc1b73e2a92db7fb91a
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publicationDate 2020-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2020034286-A1
titleOfInvention Method for preparing plecanatide
abstract A preparation method of Plecanatide comprises the following steps: 1) sequentially coupling an amino acid at position 16-7 on a solid-phase synthetic resin according to a Fmoc solid-phase synthesis strategy; 2) after removal of the Fmoc protecting group, processing a reagent for removing a Mmt protecting group and removing the side-chain Mmt protecting group of Cys at positions 7 and 15; 3) forming through bonding reaction a disulfide bond between Cys at position 7 and Cys at position 15; 4) according to the Fmoc solid-phase synthesis strategy, sequentially coupling an amino acid at position 6-1; 5) removing the Fmoc protecting group, and completing a disulfide bond between Cys at position 4 and Cys at position 12 through oxidation reaction; and 6) removing all the side-chain protecting groups, pyrolyzing the resin by using a cracking reagent, and precipitating by adding diethyl ether to obtain Plecanatide. The method is simple and efficient.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114044813-A
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priorityDate 2018-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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