http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108440530-A

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-22
filingDate 2018-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa27e43980de524242d1c691d798d16e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8937f709707dfde0f96955578ec6c0b1
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publicationDate 2018-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108440530-A
titleOfInvention A tetrahydroisoquinolinopyrrole skeleton double-spiro epoxy indole and its preparation method
abstract The invention discloses a tetrahydroisoquinolinopyrrole skeleton double-spiro epoxy indole and a preparation method thereof, belonging to the technical field of organic synthesis. In the present invention, isatin, tetrahydroisoquinoline and 3-ene oxide indole are added to a toluene solvent, trifluoroacetic acid is used as a catalyst, and a three-component [3+2] ring is generated at a temperature of 50 o C. Addition reaction to prepare double spiro indoxindole. The present invention adopts a one-pot cooking method to avoid the separation of intermediates, and after the reaction is complete, the pure product can be obtained through column chromatography or simple filtration. The invention has the advantages of mild reaction conditions, simple operation, wide substrate range and the like.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113004307-A
priorityDate 2018-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104230942-A
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Total number of triples: 23.