http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-450975-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-56
filingDate 1997-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a5c5bc37cda3299fd14feffa19fa5232
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6e31fc957592a75cddb1d1fda6b657d
publicationDate 2001-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-450975-B
titleOfInvention A process for preparing certain AZA cyclohexapeptides
abstract A process for preparing aza cyclohexapeptide compounds of the formula, wherein R1 is CH2CH2NH2 or CH2CONH2; RI is C9-C21 alkyl, C9-C21 alkenyl, C1-C10 alkoxyphenyl, C1-C10 alkoxynaphthyl, or C1-C10 alkoxyterphenyl; RII is H, C1-C4 alkyl, C3-C4 alkenyl, (CH2)2-4OH, or (CH2)2-4NRIVRV; RIII is H, C1-C4 alkyl C3-C4 alkenyl, (CH2)2-4OH, (CH2)2-4NRIVRV, or RII and RIII taken together are (CH2)4, (CH2)5, (CH2)20(CH2)2 or (CH2)2NH(CH2)2; RIV is H or Cl-C4 alkyl; RV is H or Cl-C4 alkyl; Q is N or O; or pharmaceutically acceptable acid addition salts thereof which comprises the steps of (a) reacting compound II of the formula, with phenylboronic acid, p-methoxyphenylboronic acid or methaneboronic acid to afford compound Tn of the formula, (b) which is subsequently reduced to the amine and hydrolyzed to afford compound IV of the formula, (c) which is reacted with thiophenol in a suitable solvent to afford compound V of the formula; which is stereoselectively converted to compound I by displacement of the phenylthio group.
priorityDate 1996-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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