http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2134269-C1

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filingDate 1993-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2102bf0ae6da45cade1fd6f37a73add5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d35ebb764493e36447083c81e4819164
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5546f80f55176023c2a1585e47eb45b8
publicationDate 1999-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2134269-C1
titleOfInvention Derivatives of imidazo[1,2a]thieno[2,3-d]azepines, method of their synthesis, intermediate compounds for their synthesis, pharmaceutical composition and method of its preparing
abstract FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes new derivatives of imidazo[1,2a] thieno[2,3-d] -azepines of the formula (I) or their pharmaceutically acceptable addition salt or stereochemical isomer where each of dotted line means independently a possible (complementary) bond; R 1 means hydrogen atom, C 1-4 -alkyl; R 2 means hydrogen atom, C 1-4 -alkyl, C 1-4 -alkyl substituted with hydroxycarbonyl or C 1-4 -alkylhydroxycarbonyl; R 3 means hydrogen atom, C 1-4 -alkyl; X means S-atom; L means hydrogen atom, C 1-6 -alkyl, C 1-6 -alkyl containing a substituent taken from a group including hydroxy-group, C 1-4 -alkylhydroxy-group, hydroxycarbonyl, C 1-4 -alkylhydroxycarbonyl, C 1-4 -alkylaminocarbonyl, C 1-4 -alkyl-hydroxycarbonylamino-group, C 1-4 -alkylhydroxycarbonyl-C 1-4 -alkylhydroxy-group, hydroxycarbonyl-C 1-4 -alkylhydroxy-group, C 1-4 -alkylaminocarbonylamino-group, C 1-4 -alkylaminocarbonyl- -amino-group, C 1-4 -alkylaminothiocarbonylamino-group, aryl and arylhydroxy-group; C 3-6 -alkenyl substituted with aryl where each aryl is phenyl or phenyl substituted with halogen atom, hydroxy-group, C 1-4 -alkylhydroxy-group or L means a radical of the formula -Alk-Y-Het 1 , -Alk-NH-CO-Het 2 or -Alk-Het 3 where Alk means C 1-4 -alkanediyl; Y means O-atom or NH; Het 1 means pyrimidinyl; Het 2 - furanyl; Het 3 - pyrrolyl substituted with C 1-4 -alkylhydroxycarbonyl, pyridinyl, 4,5-dihydro-5-oxo-1H-tetrazolyl substituted with C 1-4 -alkyl, 2-oxo-3-oxazolidinyl, 2,3-dihydro-2-oxo-1H-benzimidazol-1-yl or radical of the formula (II) where A-Z means a group S-CH=CH, S-CH 2 -CH 2 , S-CH 2 -CH 2 -CH 2 , CH= CH-CH=CH. Compounds show an antiallergic activity. Invention describes also a method of synthesis of the above indicated compounds, pharmaceutical composition based on said and a method of preparing the composition for treatment of patients with allergic diseases. EFFECT: improved method of synthesis, antiallergic effect. 14 cl, 90 ex
priorityDate 1992-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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