http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03135983-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-57
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
filingDate 1990-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9cd77b2a7aff62b19d509156dd9b3fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26dae1d784d176e812eecbb5a87ba164
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publicationDate 1991-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03135983-A
titleOfInvention Production of 1,1-dioxo-7-substituted cephems
abstract PURPOSE: To provide the subject cephem compound as elastase inhibitor useful for antiinflammatory and anti-denaturation agents, by oxidising a specified compound, diazotising the oxidised product, treating the product with trifluoroacetic acid, etc., converting the product into an acid halide and condensing the product. n CONSTITUTION: A compound of formula I [R 3 is (phenyl)C 1-6 alkoxy, allyloxy, C 1-6 alkoxycarbonyl-C 1-6 alkoxy] is oxidised using an aqueous hydrogen peroxide and sodium tungstate as a catalyst, thereby to give a compound of formula II. The product is diazotized and the diazo moiety is reduced with RH to give a compound of formula III. When the group R 1 is other than R 3 , the compound of formula III (R 3 is t-butoxy) is treated with trifluoroacetic acid, or the compound of formula III (R 3 is allyloxy) is treated with (Ph 3 P) 4 Pd and formic acid, thereby to yield a compound of formula IV. The product is converted into a corresponding acid halide, which is condensed with R 1 H to give an objective compound of formula V (R is C 1-6 alkoxy, etc.; R 2 is C 1-6 alkyl, etc.). n COPYRIGHT: (C)1991,JPO
priorityDate 1989-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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