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    • 1. 发明授权
    • Farnesyl protein transferase inhibiting (imidazol-5-yl) methyl-2-quinolinone derivatives
    • 法呢基蛋白转移酶抑制(咪唑-5-基)甲基-2-喹啉酮衍生物
    • US06420387B1
    • 2002-07-16
    • US09689211
    • 2000-10-12
    • Marc Gaston VenetPatrick René AngibaudPhilippe MullerGérard Charles Sanz
    • Marc Gaston VenetPatrick René AngibaudPhilippe MullerGérard Charles Sanz
    • A61K31445
    • C07D231/12C07D233/56C07D249/08C07D401/06C07D401/14C07D405/14C07D407/14C07D413/14Y02P20/55
    • This invention comprises the novel compounds of formula (I) wherein the dotted line represents an optional bond; X is oxygen or sulfur; R1 is hydrogen, C1-12alkyl, Ar1, Ar2C1-6alkyl, quinolinylC1-6alkyl, pyridylC1-6alkyl, hydroxyC1-6alkyl, C1-6alkyloxyC1-6alkyl, mono- or di(C1-6alkyl)aminoC1-6alkyl, aminoC1-6alkyl, or a radical of formula —Alk1—C(═O)—R9, —Alk1—S(O)—R9 or —Alk1—S(O)2—R9; R2, R3 and R16 each independently are hydrogen, hydroxy, halo, cyano, C1-6alkyl, C1-6alkyloxy, hydroxyC1-6akyloxy, C1-6alkyloxyC1-6alkyloxy, aminoC1-6alkyloxy, mono- or di(C1-6alkyl)aminoC1-6alkyloxy, Ar1, Ar2C1-6alkyl, Ar2oxy, Ar2C1-6alkyloxy, hydroxycarbonyl, C1-6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl; R4 and R5 each independently are hydrogen, halo, Ar1, C1-6alkyl, hydroxyC1-6alkyl, C1-6alkyloxyC1-6alkyl, C1-6alkyloxy, C1-6alkylthio, amino, hydroxycarbonyl, C1-6alkyloxycarbonyl, C1-6alkylS(O)C1-6alkyl or C1-6alkylS(O)2C1-6alkyl; R6 and R7 each independently are hydrogen, halo, cyano, C1-6alkyl, 4,4-dimethyl-oxazolyl, C1-6alkyloxy or Ar2oxy; R8 is hydrogen, C1-6alkyl, cyano, hydroxycarbonyl, C1-6alkyloxycarbonyl, C1-6alkylcarbonylC1-6alkyl; cyanoC1-6alkyl, C1-6alkyloxycarbonylC1-6alkyl, carboxyC1-6alkyl, hydroxyC1-6alkyl, aminoC1-6alkyl, mono- or di(C1-6alkyl)aminoC1-6alkyl, imidazolyl, haloC1-6alkyl, C1-6alkyloxyC1-6alkyl, aminocarbonylC1-6alkyl, or a radical of formula —O—R10, —SR10, —N—R11R12; R17 is hydrogen, halo, cyano, C1-6alkyl, C1-6alkyloxycarbonyl, Ar1; R18 is hydrogen, C1-6alkyl, C1-6alkyloxy or halo; R19 is hydrogen or C1-6alkyl; having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    • 本发明包括式(I)的新化合物,其中虚线表示任选的键; X是氧或硫; R1是氢,C1-12烷基,Ar1,Ar2C1-6烷基,喹啉基C 1-6烷基,吡啶基C 1-6烷基,羟基C 1-6烷基,C 1-6烷氧基C 1-6烷基,一或二(C 1-6烷基)氨基C 1-6烷基,氨基C 1-6烷基或 式-Alk1-C(= O)-R9,-Alk1-S(O)-R9或-Alk1-S(O)2-R9的基团; R 2,R 3和R 16各自独立地是氢,羟基,卤素,氰基,C 1-6烷基,C 1-6烷氧基,羟基C 1-6烷氧基,C 1-6烷氧基C 1-6烷氧基,氨基C 1-6烷氧基,一或二(C 1-6烷基)氨基C 1-6烷氧基 Ar 1,Ar 2 C 1-6烷基,Ar 2氧基,Ar 2 C 1-6烷氧基,羟基羰基,C 1-6烷氧基羰基,三卤代甲基,三卤代甲氧基,C 2-6烯基; R 4和R 5各自独立地是氢,卤素,Ar 1,C 1-6烷基,羟基C 1-6烷基,C 1-6烷氧基C 1-6烷基,C 1-6烷氧基,C 1-6烷硫基,氨基,羟基羰基,C 1-6烷氧基羰基,C 1-6烷基S(O) C 1-6烷基或C 1-6烷基S(O)2 C 1-6烷基; R 6和R 7各自独立地为氢,卤素,氰基,C 1-6烷基,4,4-二甲基 - 恶唑基,C 1-6烷氧基或Ar 2氧基; R 8是氢,C 1-6烷基,氰基,羟基羰基,C 1-6烷氧基羰基,C 1-6烷基羰基C 1-6