http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103554121-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_49790ed5b8ddc5fa27a1d47732c612df
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2013-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95566305917b0a34a873c0e38ca11b2b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_248df9ecd043db65ea913552e8e220e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7909fea45daddf433dc8128f6b25793f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0340350101c82fc2e754aaa07aa5f79c
publicationDate 2015-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103554121-B
titleOfInvention 3,3-spiro (2-tetrahydrofuranyl)-oxindole polycyclic compound and application thereof
abstract The invention discloses a new 3,3-spiro (2-tetrahydrofuranyl)-oxindole polycyclic compound as shown in a formula (I). The new 3,3-spiro (2-tetrahydrofuranyl)-oxindole polycyclic compound is prepared by the following steps: performing (3+2) cycloaddition on isatin diazo, aldehyde and ortho-nitro-substituted phenylene under the catalysis of rhodium acetate to construct an intermediate containing a 3, 3-spiro (2-tetrahydrofuranyl)-oxindole structure, adding a base, and then performing intramolecular Michael addition to further perform ring-closure synthesis. The compound disclosed by the invention has the property of inhibiting the activity of aurora kinase A.
priorityDate 2013-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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