http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SK-278473-B6

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-12
filingDate 1993-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0292c0a44e70734837bd919c9e338c0f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0982b31111305699fc1a3c548c08ea4c
publicationDate 1997-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-278473-B6
titleOfInvention Preparation method of 5-chloroxindole
abstract This patent describes a new procedure related to the production of 5-chloroxindole based on the chloronitrobenzene. The first stage of this procedure is closed to the reaction of chloronitobezene with a formula (II) and chloro acetic alkylester with a general formula (III), while alkali is also present and alkylester of chloronitrobenzenacetic acid is created, as a result of this reaction, this product is undertaken to the catalytic hydrogenation with the use of hydrogen, in the second stage and the appropriate amine is created, as a result of this reaction, this product is undertaken to the cyclization, in the third section, while acid is present, and the final product with a formula (I) is created.
priorityDate 1992-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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