http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S59184176-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
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filingDate 1983-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_423e7e753f0bd9e5248a34f110c9c886
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ad9acc665e580d6d0178ccf83eb05af
publicationDate 1984-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S59184176-A
titleOfInvention Production of pyrazofurin derivative
abstract PURPOSE: The reaction between 3-(2',3'-5'-O-substituted-β-D-ribofuranosyl)-4-hydroxypyrazol-5-carboxylic acid ester and an amine or a carbonylating agent gives a substituted amide derivative or pyrazolo-cyclized derivative. n CONSTITUTION: The reaction between a compound of formula I (R 1 , R 2 are benzyl or they incorporate to form isopropylidene; R 3 is benzyl, trityl or other protecting group; X is alkoxyl) and a primary or secondary amine such as morpholine or pyrrolidine) is effected by heating to form an amide, then trifluoroacetic acid or boron trichloride is made to act on the amide to effect deprotection to give a compound of formula I where R 1 WR 3 are H and X is substituted amino. Further, a compound of formula I where X is NH 2 is allowed to react with a carbonylating agent such as 1,1'-carbonylimidazole in a nonpolar solvent in the presence of a metal hydride to effect ring closure, followed by deprotection to give a compound of formula II where R 1 WR 3 are H. n USE: Antitumor and antibacterial agent. n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1983-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 30.