http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2010135196-A

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-32
filingDate 2009-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2010135196-A
titleOfInvention METHOD FOR PRODUCING 6-fluoro-1,2-dihydro-2-oxo-3n-indol-3-ylidene derivative
abstract 1. The method of obtaining 4 - [(Z) - [[4 - [(dimethylamino) methyl] phenyl] amino] (6-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene) methyl] benzenepropanoic acid represented by Formula I! ! including stages:! (a) interactions of a compound of the formula! ! from ! (i) a compound of the formula! ! or with ! (ii) a compound of the formula! ! and! (b) subsequent deesterification of the ethyl ester group of propanoic acid,! in which the removal of the acetyl group attached to the lactam group in the compound of the formula! ! in reaction (ii) is carried out after stage (a),! and in which reaction (a) (i) or (a) (ii) is carried out in the presence of a mixture of reactants and solvents selected from:! - hexamethyldisilazane and n-toluenesulfonic acid monohydrate in the presence of triethylamine; ! - hexamethyldisilazane and n-toluenesulfonic acid monohydrate in the presence of pyridine; ! - hexamethyldisilazane and benzenesulfonic acid in the presence of triethylamine; ! - hexamethyldisilazane and benzenesulfonic acid in the presence of pyridine; ! - hexamethyldisilazane and trimethylsilyl chloride; ! - N, O-bis (trimethylsilyl) acetamide and pyridine; ! - trimethylsilyl imidazolid and pyridine. ! 2. The method of obtaining 4 - [(Z) - [[4 - [(dimethylamino) methyl] phenyl] amino] (6-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene) methyl] benzenepropanoic acid according to claim 1, comprising the steps of:! (a) interactions of a compound of the formula! ! with the compound of the formula! ! and! (b) subsequent deesterification of the ethyl ester group of propanoic acid,! in which the removal of the acetyl group attached to the lactam group in the compound of the formula! ! carried out after stage (a),! and in which reaction (a) is carried out in the presence of a mixture of reactants and solvents selected from:! - hexameter
priorityDate 2008-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8314
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447496440
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425879072
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419511924
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393641
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID467861206
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8471
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135517484
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419522017
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID157075041
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413807576
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7371
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID81531
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524163
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7749
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547992
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425013245
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422222213
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425823269
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14284
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1049
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10942334
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419553602
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6397

Total number of triples: 40.