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filingDate 1991-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c82c8092ae1e86f062d9ec65ac21132d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45378ae4de6a6dd5f97f1015ee1a655a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52d5ab1f703e0c2b89c3d4299a35870b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_985fbfa106cca88608d234793e9e32b3
publicationDate 1993-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2002737-C1
titleOfInvention (-)-1-(4ъ-amino-3ъ-cyanophenyl)-2-isopropylaminoethanol or physiologically acceptable acid addition salt thereof with beta-mimetic and function-stimulating effects in animals
abstract Usage: as biologically active compounds with E-mimetic and improves the function of animals action Summary of the invention: product (-) - 1 (4 - amino - 3 - cyanophenyl) - 2 - isopropylaminoethanol or its physiologically tolerable acid additive salt, for isomer: mp 145 146 .5 &deg;C; -4.37 &amp; deg. f.aЈ0 -31 &amp;deg;; for fumarate, mp 1945 ° C; e Reagent 1: 1 (4 - amino 3 cyanophenyl) 2 "isopropylaminoethanol Reagent 2: (+) - 00 dibenzoip D of tartaric acid D Reaction conditions: in methanol at 25 - 28 ° C, followed by dissolution of the precipitate formed in boiling methanol, further filtering by distillation of a part of the solvent and holding the resulting suspension for 1 hour at 25-28 ° C. 2 tab. .
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8980832-B2
priorityDate 1990-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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