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filingDate 1974-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1976-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1425295-A
titleOfInvention Alpha-aminoylidenephthalides and processes for their preparation
abstract 1425295 α-Aminoylidenephthalides RIZHSKY ORDENA TRUDOVOGO KRASNOGO ZNAMENI POLITEKHNICHESKY INSTITUT and LATVIISKY FILIAL VSESOJUZNOGO ORDENA TRUDOVOGO KRASNOGO ZNAMENI NAUCHNO - ISSLEDOVATELSKY INSTITUT KHIMICHESKIKH REAKTIVOY I OSOBO CHISTYKH KHIMICHE SKIKH VESCHESTV 23 Jan 1974 03053/74 Heading C2C Novel α-aminoylidenephthalides of the formula wherein X is hydrogen or methoxy; R is methyl, phenyl, p-methoxyphenyl, p-chlorophenyl or p-bromophenyl; R<SP>1</SP> is hydrogen, methyl, ethyl or butyl; R<SP>11</SP> is hydrogen, methyl, ethyl, propyl, butyl, cyclohexyl, benzyl, phenyl, tolyl, p-methoxyphenyl, p-chlorophenyl or pbromophenyl; or R<SP>1</SP>R<SP>11</SP> is a radical of the formula -(CH 2 ) 2 -O-(CH 2 ) 2 -, -(CH 2 ) 4 - or -(CH 2 ) 5 -, are prepared by isomerizing a 2- amino-indanedione-1,3 of the formula in an organic solvent in the presence of a basic nucleophilic catalyst at the boiling temperature of the solvent. The catalyst is suitably sodium methoxide, ethoxide or phenoxide, a solution of potassium hydroxide in methanol or ethanol, piperidine or triethylamine. The novel compounds possess pharmaceutical properties.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9833423-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016185967-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9951058-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9790197-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9890133-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4605738-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014523416-A
priorityDate 1974-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 46.