http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2308451-C2

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filingDate 2002-09-12^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-10-20^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f862bcd6d8fe89d5932ffc92a950370
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83bb23493039f187443bc443aa9305c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_096e587bde1b3f4439cb3539bca5f20a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51eadca18c63f2cda408880a80626622
publicationDate 2007-10-20^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2308451-C2
titleOfInvention Methods for production of racemic aminosubstituted 5,6,7,8-tetrahydroquinoline or racemic aminosubstituted 5,6,7,8-tetrahydroisoquinoline, methods for separation and racemization thereof, methods for production of ketosubstituted 5,6,7,8-tetrahydroquinoline or ketosubstituted 5,6,7,8-tetrahydroisoquinoline, method for production of enantiomer pf condensed bycyclic ring substituted with primary amine, 5,6,7,8-tetrahydroquinoline derivatives
abstract FIELD: organic chemistry, in particular methods for production and separation of racemic aminosubstituted condensed bycyclic ring systems. n SUBSTANCE: in one embodiment claimed method includes selective hydration of aminosubstituted aminosubstituted condensed aromatic ring system. In alternative embodiment claimed method includes preparation of racemic aminosubstituted condensed bycyclic ring system by nitrozation. Moreover invention relates to enzymatic resolution of racemic mixture to produce (R)- and (S)-forms of aminosubstituted condensed bycyclic rings as well as to racemization method for secondary preparation of non-preferable enantiomer. Also disclosed is method for production of enantiomer of condensed bycyclic ring substituted with primary amine by preparation of respective enantiomerically pure imine of condensed bycyclic ring, diastereoselective reducing thereof and elimination of auxiliary chiral fragment. In abovementioned processes compounds of formulae I, II, III, IV, V, VI, VII, VIII, XIII, XIX which are described in specification together with radical meanings. Moreover invention relates to 5,6,7,8-tetrahydroquinoline derivatives such as N-(2-methyl-5,6,7,8-tetrahydroquinolin-4-yl)-acetamide, N-(1,2,3,4-tetrahydroquinolin-7-yl)-acetamide, (R,S)-N-(2-methyl-5,6,7,8-tetrahydroquinolin-8-yl)-acetamide, etc. n EFFECT: effective methods for production of racemates and enantiomers of various ring systems. n 44 cl, 37 ex, 2 tbl
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-024637-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MD-4375-C1
priorityDate 2001-09-12^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396401
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA0A3Q1M1X5
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419491068
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6737
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID511
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409768956
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14487
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID187940
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6421
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18196

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