http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5220031-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-06078
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-40
filingDate 1991-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe71b2e6990cb9da347f7d7f2d7ee932
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca4b68ec6b414e48b4ead372110674f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bb4a3a905c64a1b60581b8005322d77
publicationDate 1993-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5220031-A
titleOfInvention Process for the preparation of [1S-(1R*,2S*3R*)]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl-N-[(cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide
abstract An improved process for the preparation of [1S-(1R*,2S*,3R*) ]-N-(4-morpholinylsulfonyl)-L-phenylalanyl-3-(2-amino-4-thiazolyl)-N-[(1-cyclohexylmethyl)-2,3-dihydroxy-5-methylhexyl]-L-alaninamide is described where the key intermediate, 3-(2-amino-4-thiazolyl)-L-alanine is converted without protecting the aminothiazole group to the desired compound, as well as valuable intermediates used in the process.
priorityDate 1991-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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