首页> 外国专利> New N-benzyloxycarbonyl-tyrosine hydrazide derivatives as selective inhibitors of phosphodiesterase-IV, useful for treating e.g. myocardial diseases, asthma, chronic bronchitis and atopic dermatitis

New N-benzyloxycarbonyl-tyrosine hydrazide derivatives as selective inhibitors of phosphodiesterase-IV, useful for treating e.g. myocardial diseases, asthma, chronic bronchitis and atopic dermatitis

机译:新的N-苄氧基羰基-酪氨酸酰肼衍生物作为磷酸二酯酶-IV的选择性抑制剂,可用于治疗例如心肌疾病,哮喘,慢性支气管炎和特应性皮炎

摘要

N-benzyloxycarbonyl-tyrosine hydrazide derivatives (I) and their salts and solvates, as L and or D enantiomers, are new. N-benzyloxycarbonyl-tyrosine hydrazide derivatives of formula (I) and their salts and solvates, as L and or D enantiomers, are new; R1, R2 = hydrogen, hydroxy, OR5, SR5, SOR5, SO2R5, halo or together form methylenedioxy; R3, R4 = R5 or as defined for R1 and R2; R5 = 1-10C alkyl, optionally substituted by 1-5 fluoro and/or chloro, 3-7C cycloalkyl, 5-10C alkylenecycloalkyl or 2-8C alkenyl; halo = fluoro, chloro, bromo or iodo. Independent claims are also included for: (1) a method for preparing (I); and (2) intermediates of formula (III). All definitions are as above.
机译:N-苄氧基羰基-酪氨酸酰肼衍生物(I)及其盐和溶剂化物,作为L和/或D对映异构体,是新的。式(I)的N-苄氧基羰基-酪氨酸酰肼衍生物及其盐和溶剂化物是L和/或D对映异构体,是新的。 R 1,R 2 =氢,羟基,OR 5,SR 5,SOR 5,SO 2 R 5,卤素或一起形成亚甲基二氧基; R 3,R 4 = R 5或如对于R 1和R 2所定义; R 5 = 1-10C烷基,任选地被1-5个氟和/或氯,3-7C环烷基,5-10C亚烷基环烷基或2-8C烯基取代;卤素=氟,氯,溴或碘。独立权利要求还包括:(1)一种制备方法(I); (2)式(III)的中间体。所有定义如上。

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