http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-403324-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_47c7bbe952d2db7a86a178db094082b0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-10
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filingDate 2013-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a163d7a4005d8d24fd16e4fdb5bda49
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publicationDate 2014-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-403324-A1
titleOfInvention 3,5-disubstituted and 3,4,5-tri-substituted isoxazoles and the method of their preparation
abstract The subject of the invention are 3,5-disubstituted and 3,4,5-trisubstituted isoxazoles of the general formulas 1a, 1b, 1c and 1d, where: Ar - is a substituted mono- or polynuclear aryl group, in particular 2,4-dichlorophenyl, 2 ,4-dibromophenyl, 2,4-difluorophenyl, 2,6-dichlorophenyl, 2,4-dimethylphenyl, 2,4-dimethoxyphenyl, 3,4-methylenedioxyphenyl, 2,6-dimethylphenyl, 2,6-difluorophenyl, 2,4 ,6-trimethylphenyl, 2,4,6-trimethoxyphenyl, 9-anthracenyl; Q - is a sterically built, substituted or unsubstituted, mono- or polynuclear aryl group, in particular 2,2'-bitiophen-5-yl, 9-anthracenyl, 1-naphthyl; A - is a linker in the form of a difunctional aryl or heteroaryl group, in particular 1,2-phenylene, 1,3-phenylene, 1,4-phenylene, anthracene-9,10-diyl. The invention also includes a method for their preparation in dipolar cycloaddition reactions of aromatic nitrile oxides or aromatic dinitrile dioxides to mono- and symmetrically disubstituted alkynes, in solvents such as short-chain alcohols, diethyl ether, saturated haloalkanes, acetone or preferably methylene chloride or any mixtures thereof. The substrates of these reactions are low-reactive dipoles and sterically developed dipolarophiles. The reactions are carried out under high pressure, from 0.5 to 2.0 GPa, at a temperature from 10 to 110°C, for 1 to 48 hours, in an inert gas atmosphere, preferably argon. Compounds obtained in this way can be used, among others, as pharmaceuticals, substrates for further syntheses or precursors of nanomaterials for organic electronics.
priorityDate 2013-03-27-04:00^^<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: 34.