发明名称 1,3-DIHYDRO-1-(PHENYLALKYL)-2H-IMIDAZOL-2-ONE DERIVATIVES HAVING PDE IV AND CYTOKINE ACTIVITY
摘要 Provided are compounds of the formula depicted and including the N-oxide form, salts and sterochemically isomeric forms thereof having PDE IV inhibiting activity as well as cytokine inhibiting activity. R1 and R2 are independently hydrogen, alkyl, difluoromethyl, trifluoromethyl, cycloalkyl, heterocyclic radical, alkylsulfonyl, arylsulfonyl, aralkyl or heterocyclic substituted alkyl; R3 is hydrogen, halo or alkoxy; R4 is hydrogen, halo, optionally substituted alkyl, cycloalkyl, carboxyl, alkoxycarbonyl, cycloalkylaminocarbonyl, aryl or hetercyclic radical; or R4 is -O-R6 or -NH-R7; R5 is hydrogen, halo, hydroxy or alkyl; or R4 and R5 taken together may form a bivalent alkylene radical optionally interrupted with O or NR8; Y is a bond, haloalkanylene or alkanylene; A-B is an optionally substituted bivalent ethyl or ethenyl hydrocarbon radical; and L is hydrogen, alkylcarbonyl, alkoxycarbonyl, an optionally substituted alkyl, alkenyl, arylalkenyl an optionally substituted piperidinyl, alkylsulfonyl or arylsulfonyl.
申请公布号 NZ304877(A) 申请公布日期 1999.06.29
申请号 NZ19960304877 申请日期 1996.03.28
申请人 JANSSEN PHARMACEUTICA NV 发明人 FREYNE, EDDY JEAN EDGARD;DIELS, GASTON STANISLAS MARCELLA;ANDRES-GIL, JOSE IGNACIO;FERNANDEZ-GADEA, FRANCISCO JAVIER
分类号 C07D233/32;A61K31/415;A61K31/4166;A61K31/44;A61K31/4427;A61K31/443;A61P11/00;A61P17/00;A61P29/00;A61P37/08;C07D233/36;C07D233/38;C07D233/70;C07D401/06;C07D401/12;C07D405/06;C07D405/12;(IPC1-7):C07D233/70;C07D233/90 主分类号 C07D233/32
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