http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CO-5680431-A2

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb66d9373d09efad73c142762f6dfb00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2006-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36302bb12c7eb2de4405ce1a2d82f913
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18a5ee54411ed93f13886c1bbf71f514
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publicationDate 2006-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CO-5680431-A2
titleOfInvention PROCEDURE FOR THE PREPARATION OF AMINOCROTONILO COMPOUNDS
abstract 1. Process for the preparation of a compound of the general formula (VII) in which X means a methine group or a nitrogen atom, Ra means a benzyl, 1-phenylethyl or 3-chloro-4-fluorophenyl group and R3 and R4 means a linear or branched C1-4 alkyl group, which encompasses the following synthesis steps: a) reaction of a compound of the general formula (V) in which X means a methine group or a nitrogen atom and Ra means a benzyl, 1-phenylethyl or 3-chloro-4-fluorophenyl group, in suitable solvents after the corresponding activation with di- (C1-4 alkyl) -phosphonoacetic acid and b) reaction of the compound of the general formula (VI) thus obtained in which X means a methine group or a nitrogen atom, Ra means a benzyl, 1-phenylethyl or 3-chloro-4-fluorophenyl group and R1 means a linear or branched C1-4 alkyl group, with the aldehyde of the formula in which R3 and R4 mean in each case a C1-C4 alkyl group of cade na linear or branched, the radicals being the same or different, or a corresponding equivalent of aldehyde with the use of suitable organic or inorganic bases.
priorityDate 2006-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 21.