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filingDate 1990-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8570012a3e8a1d746391fcc8eae1269c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38fb3a68906fa7269fd308d0b4569793
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a8db616ebb9d3ce6aa5756bbe5a4361
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c88613d44170c79c7d6f7c3e6332015
publicationDate 1997-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2084453-C1
titleOfInvention Method of synthesis of aromatic derivatives or their salts with organic or inorganic acids or their racemates
abstract FIELD: organic chemistry. SUBSTANCE: invention relates to synthesis of aromatic compounds of the general formula (I) (see invention description) where: m = 2, 3; Ar and Ar 1 were taken from thienyl, free of substituted phenyl, benzothienyl, naphthyl, biphenyl, indolyl; X and X' - are different or similar and mean hydrogen and other - hydrogen, hydroxyl or forms with X'' the bond carbon-carbon, or together with X and X' form oxo- or dialkylaminoalkoxyimino-group; Y - N or C(X''); Q, R, T, Z and M have different values. Reagent 1: compound of the formula (II) . Reagent 2: compound of the formula (III) HOCOZ or (IV') W=C=N-Z. Compound (IV) is synthesized from which tetrapyranylhydroxy-group is split off by mild acid hydrolysis and the obtained N-protected alkanolamine of the formula (V) is treated with methanesulfonylchloride and mesilate of the formula (VI) is obtained that is treated with secondary amine of the formula (VII) . Then protective groups were split off and converted to salt. Synthesized compounds were used in chemical-pharmaceutical industry. EFFECT: improved method of synthesis. 5 cl, 11 tbl
priorityDate 1989-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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