http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2074181-C1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-12
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filingDate 1992-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0263a826f10d303601c7c0ae673baea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f630c0e9afc7442b728ced2e0bf2df6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dea88b829aa2224bc936d2980718ae70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a4e7ae068a6af05d48c534c2bd7a98b
publicationDate 1997-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2074181-C1
titleOfInvention 1-alkyl, 1-alkenyl or 1-alkynylaryl-2-amino-1,3-propanediols or their optical isomers or pharmaceutically acceptable salts and method of their synthesis
abstract FIELD: organic chemistry. SUBSTANCE: products: 1-alkyl, 1-alkenyl or 1-alkynylaryl-2-amino-1,3-propanediols were synthesized by interaction of halogenpyridine with phenylalkyne in acid accepting agent and in the presence of bis-(triphenylphosphine)-palladium/copper iodide dichloride at 0-75 C. Synthesized compounds were used in medicine for memory disorder treatment. EFFECT: improved method of synthesis. 3 cl, 4 dwg, 7 tbl
priorityDate 1990-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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