http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2379293-C2

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filingDate 2005-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40df27b7a408d97cfddb71a05476925c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e3d478d35c32d8931c7091b3911e4ae
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publicationDate 2010-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2379293-C2
titleOfInvention 2h- or 3h-benzo[e]indazol-1-yl-carbamate derivatives and use thereof in therapy
abstract FIELD: chemistry. n SUBSTANCE: invention relates to compounds with general formula (I), where W is oxygen or sulphur; X 1 and X 3 are independently hydrogen or C 1 -C 6 -alkoxy; X 2 is hydrogen, halogen, C 1 -C 6 -alkyl or C 1 -C 6 -alkoxy and X 4 is hydrogen, Y is in position (N2) or (N3); when Y is in position (N2), Y is C 1 -C 6 -alkyl, C 1 -C 6 -fluoroalkyl, phenyl, pyridinyl or pyrazinyl; when Y is in position (N3), Y is phenyl, pyridinyl or pyrimidinyl, where phenyl is optionally substituted with one or more atoms or groups selected from halogen, C 1 -C 5 alkyl, C 1 -C 6 -alkoxy; the bond in position C 4- C 5 is a single or double bond; R 1 and R 2 each independently represent phenyl and C 1 -C 6 -alkyl, where at least one of R 1 and R 2 represents C 1 -C 6 -alkyl; or R 1 and R 2 together with the nitrogen atom to which they are bonded form a cyclic group containing from 4 to 7 links and a nitrogen atom and possibly another heteroatom, such as nitrogen or oxygen, possibly substituted with one or more C 1 -C 6 -alkyl groups; or to their pharmaceutically acceptable salts. The invention also relates to methods of producing the proposed compounds with formula (I), and specifically to compounds with formulae (Ia) and (Ib), in which X 1 , X 3 , X 3 , X 4 and Y are as described in general formula (I). The invention also relates to intermediate compounds of synthesis of formula (I) compounds - compounds with formulae (Va) and (Vb). In formula (Va) X 1 , X 3 and X 4 represent hydrogen; X 2 is hydrogen, halogen or C 1 -C 6 -alkoxy and Y is C 1 -C 6 -alkyl, C 1 -C 6 -fluoroalkyl, phenyl, pyridinyl or pyrazinyl; where phenyl is possibly substituted with one or more atoms or groups selected from halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy. In formula (Vb) X 1 and X 3 represent hydrogen or C 1 -C 6 -alkoxy; X 2 is hydrogen, halogen, C 1 -C 6 -alkyl or C 1 -C 6 -alkoxy, X 4 is hydrogen; Y is phenyl, pyridinyl or pyrmidinyl; phenyl is possibly substituted with one or more atoms or groups selected from halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy. The invention also relates to a medicinal agent based on a formula (I) compound or its pharmaceutically acceptable salt for preventing and treating pathologies where peripheral type benzodiazepine receptors take part. The invention also relates to use of formula (I) compounds in preparing the said medicinal agent and to a pharmaceutical composition for preventing and treating pathologies in which peripheral type benzodiazepine receptors take part. n EFFECT: new compounds have useful biological activity. n 11 cl, 3 tbl, 6 ex n .
priorityDate 2004-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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