发明名称 RESPIRATORY SYNCYTIAL VIRUS REPLICATION INHIBITORS
摘要 <p>This invention concerns the compounds of formula (I), prodrugs, <I>N</I>-oxides, addition salts, quaternary amines, metal complexes or stereochemically isomeric forms thereof wherein -a<1>=a<2>-a<3>=a<4>- is a radical of formula -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- wherein each hydrogen atom may optionally be substituted; Q is a radical of formula (b-1), (b-2), (b-3), (b-4), (b-5), (b-6), (b-7), (b-8), wherein Alk is C1-6alkanediyl; Y<1> is a bivalent radical of formula-NR<2>- or -CH(NR<2>R<4>)-; X<1> is NR<4>, S, S(=O), S(=O)2, O, CH2, C(=O), CH(=CH2), CH(OH), CH(CH3), CH(OCH3), CH(SCH3), CH(NR<5a>R<5b>), CH2-NR<4> or NR<4>-CH2; X<2> is a direct bond, CH2, C(=O), NR<4>, C1-4alkyl-NR<4>, NR<4>-C1-4alkyl; t is 2 to 5; u is 1 to 5; v is 2 or 3; and whereby each hydrogen in Alk and in (b-3), (b-4), (b-5), (b-6), (b-7) and (b-8), may optionally be replaced by R<3>; provided that when R<3> is hydroxy or C1-6alkyloxy, then R<3> can not replace a hydrogen atom in the alpha position relative to a nitrogen atom; G is substituted C1-10alkanediyl wherein the substituent is attached via an oxygen atom; R<1> is an optionally substituted monocyclic heterocycle or aryl; R<2> is hydrogen, formyl, C1-6alkylcarbonyl, Hetcarbonyl, pyrrolidinyl, piperidinyl, homopiperidinyl, C3-7cycloalkyl or C1-10alkyl substituted with N(R<6>)2 and optionally with another substituent; R<3> is hydrogen, hydroxy, C1-6alkyl, C1-6alkyloxy, arylC1-6alkyl or arylC1-6alkyloxy; R<4> is hydrogen, C1-6alkyl or arylC1-6alkyl; R<5a>, R<5b>, R<5c> and R<5d> are hydrogen or C1-6alkyl; or R<5a> and R<5b>, or R<5c> and R<5d> taken together form a bivalent radical of formula -(CH2)s- wherein s is 4 or 5; R<6> is hydrogen, C1-4alkyl, formyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl or C1-6alkyloxycarbonyl; aryl is optionally substituted phenyl; Het is pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl; as respiratory syncytial virus replication inhibitors; their preparation, compositions containing them and their use as a medicine.</p>
申请公布号 WO0100612(A2) 申请公布日期 2001.01.04
申请号 WO2000EP05675 申请日期 2000.06.20
申请人 JANSSEN PHARMACEUTICA N.V.;JANSSENS, FRANS, EDUARD;MEERSMAN, KATHLEEN, PETRUS, MARIE-JOSE;SOMMEN, FRANCOIS, MARIA;ANDRIES, KOENRAAD, JOZEF, LODEWIJK, MARCEL 发明人 JANSSENS, FRANS, EDUARD;MEERSMAN, KATHLEEN, PETRUS, MARIE-JOSE;SOMMEN, FRANCOIS, MARIA;ANDRIES, KOENRAAD, JOZEF, LODEWIJK, MARCEL
分类号 A61K31/437;A61K31/4465;A61K31/454;A61K31/4545;A61K45/00;A61P11/00;A61P31/12;A61P31/14;A61P43/00;C07B61/00;C07D401/12;C07D401/14;C07D471/04;(IPC1-7):C07D401/12;A61K31/446 主分类号 A61K31/437
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