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Aryloxycycloalkenyl and aryloxyiminocyclo-alkenylhydroxyureas

机译:芳氧基环烯基和芳氧基亚氨基环烯基羟基脲

摘要

N-(Aryloxy or aryloxyimino)cycloalkylenyl-N-hydroxyurea derivs. of formula (I), their salts and prodrugs, are new: Ar = phenyl, naphthyl, or biphenyl (all opt. substd. by 1-3 1-4C alkyl, haloalkyl, hydroxyalkyl, alkoxy, haloalkoxy, or alkylthio, 2-4C alkoxyalkoxy, OH, halo, CN, NH2, mono- or di-(1-4C alky)amino, 2-6C alkanoylamino, COOH, 2-6C alkoxycarbonyl, or phenyl, phenoxy, phenylthio, or phenylsulphinyl (all opt. substd. by 1-3 Q) or furyl, benzo(b)furyl, thienyl, benzo(b)thienyl, pyridyl, or quinolyl (all opt. substd. by 1-3 1-4C alkyl, haloalkyl, or alkoxy, halo,OH, or phenyl, phenoxy or phenylthio (all opt. substd. by 1-3 Q)); Q = 1-4C alkyl, haloalkyl, alkoxy, or haloalkoxy, cyano or halo; X = 1-4C alkylene, 2-4C alkenylene, (CHR1)mQ1(CHR2)n, O(CHR1)jQ2; or (CHR1)ON= (with the N attached to cycloalkene ring); Q1 = O, S, SO, SO2, NR3, CH=NO, or CO, Q2 = O, S, SO, SO2, or NR3; R1-R3, Z = H or 1-4C alkyl; m, n = 0-4; j = 1-4; p = 1 or 2; Y = H, or 1-4C alkyl, haloalkyl, alkoxy, or alkylthio, 2-4C alkoxyalkyl, OH, halo, CN, or NH2; and M = H, a cation, or a metabolically cleavable gp.
机译:N-(芳氧基或芳氧基亚氨基)环亚烷基-N-羟基脲衍生。式(I)的式,它们的盐和前药是新的:Ar =苯基,萘基或联苯(均由1-3 1-4C烷基,卤代烷基,羟烷基,烷氧基,卤代烷氧基或烷硫基取代) 4C烷氧基烷氧基,OH,卤素,CN,NH2,单或二-(1-4C烷基)氨基,2-6C烷酰基氨基,COOH,2-6C烷氧基羰基或苯基,苯氧基,苯硫基或苯基亚磺酰基(全部选择。 (例如1-3 Q)或呋喃基,苯并(b)呋喃基,噻吩基,苯并(b)噻吩基,吡啶基或喹啉基(均由1-3 1-4C烷基,卤代烷基或烷氧基,卤素, OH,或苯基,苯氧基或苯硫基(全都被1-3 Q取代); Q = 1-4C烷基,卤代烷基,烷氧基或卤代烷氧基,氰基或卤素; X = 1-4C亚烷基,2-4C亚烯基,(CHR1)mQ1(CHR2)n,O(CHR1)jQ2;或(CHR1)ON =(N与环烯烃环相连); Q1 = O,S,SO,SO2,NR3,CH = NO或CO,Q2 = O,S,SO,SO2或NR3; R1-R3,Z = H或1-4C烷基; m,n = 0-4; j = 1-4; p = 1或2; Y = H,或1-4C烷基,卤代烷基,烷氧基或烷硫基,2-4C烷氧基烷基,OH,卤素,CN或NH2;并且M = H,阳离子或可代谢裂解的gp。

著录项

  • 公开/公告号IL115853D0

    专利类型

  • 公开/公告日1996-01-31

    原文格式PDF

  • 申请/专利权人 PFIZER INC;

    申请/专利号IL19950115853

  • 发明设计人

    申请日1995-11-02

  • 分类号6C07CA;

  • 国家 IL

  • 入库时间 2022-08-22 03:53:42

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