http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20110098673-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-404
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08
filingDate 2011-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31929264c518d64a70ed0c606cdba16d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e609af7841742852d9693c0040ef727c
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publicationDate 2011-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20110098673-A
titleOfInvention Method for preparing indole derivative using one step continuous ring reaction
abstract The present invention relates to an indole derivative and a method for preparing the same, and more particularly, to quickly and simply prepare an indole derivative, which is the most basic compound among alkaloids used in the pharmaceutical field, according to the following Reaction Scheme (1). It is about how to. <Scheme 1> Wherein R 1 is hydrogen, phenyl, methoxy methylbenzene, cyclohexyl, butylbenzoate, tertiarybutyl ethoxydimethyl silane, butyl tertiary butyl, naphthyl, methoxybenzene, butylthiobenzene or butylsulfonyl Selected from the group consisting of benzene, R 2 is selected from hydrogen, methyl ester, nitrile or butylsulfonyl, R 3 is selected from hydrogen, nitro, methoxy or butoxy groups, and R 4 is selected from hydrogen or decyl groups Is selected.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102924358-A
priorityDate 2010-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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