发明名称 СОЕДИНЕНИЯ, ОБЛАДАЮЩИЕ АКТИВНОСТЬЮ АНТАГОНИСТОВ CRTH2 РЕЦЕПТОРОВ
摘要 Compounds of general formula (I): wherein R<SUP>1</SUP>, R<SUP>2</SUP>, R<SUP>3 </SUP>and R<SUP>4 </SUP>are independently hydrogen, halo, C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, -O(C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl), -CON(R<SUP>9</SUP>)<SUB>2</SUB>, -SOR<SUP>9</SUP>, -SO<SUB>2</SUB>R<SUP>9</SUP>, -SO<SUB>2</SUB>N(R<SUP>9</SUP>)<SUB>2</SUB>, -N(R<SUP>9</SUP>)<SUB>2</SUB>, -NR<SUP>9</SUP>COR<SUP>9</SUP>, -CO<SUB>2</SUB>R<SUP>9</SUP>, -COR<SUP>9</SUP>, -SR<SUP>9</SUP>, -OH, -NO<SUB>2 </SUB>or -CN; each R<SUP>9 </SUP>is independently hydrogen or C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl; R<SUP>5 </SUP>and R<SUP>6 </SUP>are each independently hydrogen, or C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl or together with the carbon atom to which they are attached form a C<SUB>3</SUB>-C<SUB>7 </SUB>cycloalkyl group; R<SUP>7 </SUP>is hydrogen or C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl n is 1 or 2; X is a bond or, when n is 2, X may also be a NR<SUP>9 </SUP>group; wherein R<SUP>9 </SUP>is as defined above; when X is a bond R<SUP>8 </SUP>is C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, C<SUB>2</SUB>-C<SUB>6 </SUB>alkenyl, C<SUB>2</SUB>-C<SUB>6 </SUB>alkynyl, biphenyl or a 9-14 membered bicyclic or tricyclic heteroaryl group; when X is a NR<SUP>9 </SUP>group R<SUP>8 </SUP>may additionally be phenyl, naphthyl or a 5-7 membered heteroaromatic ring; and the R<SUP>8 </SUP>group is optionally substituted with one or more substituents selected from halo, C<SUB>1</SUB>-C<SUB>6 </SUB>alkyl, -O(C<SUB>1</SUB>-C<SUB>6</SUB>)alkyl, aryl, -O-aryl, heteroaryl, -O-heteroaryl, -CON(R<SUP>9</SUP>)<SUB>2</SUB>, -SOR<SUP>9</SUP>, -SO<SUB>2</SUB>R<SUP>9</SUP>, SO<SUB>2</SUB>N(<SUP>9</SUP>)<SUB>2</SUB>, -N(<SUP>9</SUP>)<SUB>2</SUB>, -NR<SUP>9</SUP>COR<SUP>9</SUP>, -CO<SUB>2</SUB>R<SUP>9</SUP>, -COR<SUP>9</SUP>, -SR<SUP>9</SUP>, -OH, -NO<SUB>2 </SUB>or -CN; wherein R<SUP>9 </SUP>is as defined above; and their pharmaceutically acceptable salts, hydrates, solvates, complexes and prodrugs are useful in the treatment of allergic diseases such as asthma, allergic rhinitis and atopic dermatitis.
申请公布号 RU2006109108(A) 申请公布日期 2007.11.20
申请号 RU20060109108 申请日期 2004.10.13
申请人 Оксаген Лимитед (GB) 发明人 МИДЛЕМИС Девид (GB);ЭШТОН Марк Ричард (GB);БОЙД Эдвард Эндрю (GB);БРУКФИЛД Фредерик Артур (GB);АРМЕР Ричард Эдвард (GB);ПЕТИФЕР Эрик Рой (GB)
分类号 C07D209/30;C07D401/12;C07D403/12;C07D417/12 主分类号 C07D209/30
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