首页> 外国专利> New aryl-substd. hydroxamic acid and N-hydroxy-lactam cpds. - lipoxygenase and/or cyclo:oxygenase inhibitors e.g. as analgesic, antiinflammatory, antipyretic and antiallergic agents

New aryl-substd. hydroxamic acid and N-hydroxy-lactam cpds. - lipoxygenase and/or cyclo:oxygenase inhibitors e.g. as analgesic, antiinflammatory, antipyretic and antiallergic agents

机译:新的芳基取代。异羟肟酸和N-羟基内酰胺-脂加氧酶和/或环加氧酶抑制剂,例如。作为止痛,消炎,解热和抗过敏药

摘要

Cpds. of formula (I) and salts are new. Ar-(L-Ar')q-(X)k-(Y)p-Q (I) Where k, p and q each=0 or 1, provided that when k=1 then p=1; Ar=(i) naphthyl, tetrahydronaphthyl or pyridyl, all opt. substd. by 1 or more of 1-4C alkyl, haloalkyl or alkoxy, halogen, NO2, NH2, carboxy, 1-4C alkoxycarbonyl or OH, or (ii) phenyl, opt. substd. as in (i) or by phenyl, itself opt. substd. as in (i); L=-(CH2)r- (r=1-4), -O-, -CH2O-, -CH2S-, -OCH2-, -CONH-, -NHCO-, -CO- or -CH2NH-; Ar'=phenylene, thienylene or pyridylene, all opt. substd. as in (i); X=O, S or CO, provided that at least 1 atom. separates CO from any CO gp. in Q (below); Y=1-10C alkylene or alkenylene; Q=1-hydroxy-1,3-dihydro-imidazol-2-one or a gp. of formula (II) or (III); m=O and n=1 or m=1 and n=O; when n=1: R1 and R2 each=H or 1-4C alkyl, or R2 may also be 5-7C cycloalkyl; when m=1: R1=H, 1-4C alkyl, COR3 or a value of Ar, and R2=H, 1-4C alkyl, NH2, 1-4C alkylamino, di(1-4C alkyl)amino; 5-7C cycloalkylamino, 5-7C cycloalkyl (1-4C alkyl)amino; anilino, N-1-4C alkyl-anilino or a value of Ar; R3=1-4C alkyl (opt. substd. by carboxy or 1-4C alkoxycarbonyl) or -NR4R5; R4=H or 1-4C alkyl; R5=H, 1-4C alkyl or phenyl opt. substd. by substit(s)., as in (i); and Z=2-5C alkylene in which a C atom may be replaced by a heteroatom.
机译:Cpds。式(I)的化合物和盐是新的。 Ar-(L-Ar')q-(X)k-(Y)p-Q(I)其中k,p和q分别为0或1,条件是当k = 1时p = 1; Ar =(i)萘基,四氢萘基或吡啶基,全部选择。取代选用1-4C烷基,卤代烷基或烷氧基,卤素,NO 2,NH 2,羧基,1-4C烷氧基羰基或OH中的一种或多种,​​或(ii)苯基。取代如(i)中所述或通过苯基,其自身选择。取代如(i)中所述; L =-(CH 2)r-(r = 1-4),-O-,-CH 2 O-,-CH 2 S-,-OCH 2-,-CONH-,-NHCO-,-CO-或-CH 2 NH-。 Ar′=亚苯基,亚噻吩基或亚吡啶基,全部选择。取代如(i)中所述; X = O,S或CO,条件是至少1个原子。从任何CO gp中分离出CO。在Q中(如下); Y = 1-10C亚烷基或亚烯基; Q = 1-羟基-1,3-二氢-咪唑-2-酮或gp。具有式(II)或(III); m = O且n = 1或m = 1且n = O;当n = 1时,R 1和R 2各自为H或1-4C烷基,或R 2也可以为5-7C环烷基;当m = 1时:R1 = H,1-4C烷基,COR3或Ar的值,并且R2 = H,1-4C烷基,NH2,1-4C烷基氨基,二(1-4C烷基)氨基; 5-7C环烷基氨基,5-7C环烷基(1-4C烷基)氨基;苯胺基,N-1-4C烷基-苯胺基或Ar的值; R3 = 1-4C烷基(被羧基或1-4C烷氧羰基取代)或-NR4R5; R4 = H或1-4C烷基; R5 = H,1-4C烷基或苯基。取代如(i)中所述,由替代人组成; Z = 2-5C亚烷基,其中C原子可以被杂原子取代。

著录项

  • 公开/公告号ES8800130A1

    专利类型

  • 公开/公告日1988-01-01

    原文格式PDF

  • 申请/专利权人 THE WELLCOME FOUNDATION LIMITED;

    申请/专利号ES19860553012

  • 发明设计人

    申请日1986-03-14

  • 分类号C07C83/10;

  • 国家 ES

  • 入库时间 2022-08-22 06:57:19

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