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Beta-phenylalkanoic acids esters and amides having - analgesic and anti-inflammatory activity

机译:具有镇痛和抗炎活性的β-苯基链烷酸酯和酰胺

摘要

Beta-phenylalkanoic acids esters and amides having analgesic and anti-inflammatory activity. M3A. Are new compounds of formula (I): including the salts of the acids and optical isomers. (X = COOH, esterified or as an amide; A = OH, alkoxy, alkenyloxy, acyloxy; B = aliphatic hydrocarbyl, H; A with B may form a direct bond; B with R2 may form an alkylene chain; R' and R2 = H, aliphatic hydrocarbyl; Ph = phenylene; R = opt. substd. cycloaliphatic hydrocarbyl). Uses as analgesic and anti-inflammatory agents, also as intermediates for other drugs. Preferred cpds. are of formula: (R4 = 1-cycloalkenyl (C5-C7), opt. substd. by alkoxy, alkyl; R5 = H, alkyl; A' = OH; B' = H, alkyl; or A' + B' = direct bond; Rz = alkoxy (C1-C4), NH2, OH); esp. the cpd. Preparation by conventional methods; also by isomerisation with double-bond removal of novel intermediates of formula: (Ro = aliphatic hydrocarbylene), e.g. by use of strong alkalis or acids.
机译:具有止痛和抗炎活性的β-苯基链烷酸酯和酰胺。 M3A。是式(I)的新化合物:包括酸的盐和旋光异构体。 (X = COOH,被酯化或作为酰胺; A = OH,烷氧基,链烯氧基,酰氧基; B =脂族烃基,H; A与B可以形成直接键; B与R2可以形成亚烷基链; R'和R2 = H,脂族烃基; Ph =亚苯基; R =最佳取代环脂族烃基)。用作止痛药和消炎药,也用作其他药物的中间体。首选的cpds。具有下式的通式:(R 4 = 1-环烯基(C 5 -C 7),优选被烷氧基烷基取代; R 5 = H,烷基; A′= OH; B′= H,烷基;或A′+ B′=直接键; Rz =烷氧基(C1-C4),NH2,OH);尤其是cpd。通过常规方法制备;也可通过异构化并双键去除式(R 1 =脂族亚烃基)的新型中间体,例如。通过使用强碱或强酸。

著录项

  • 公开/公告号CH528468A

    专利类型

  • 公开/公告日1972-09-30

    原文格式PDF

  • 申请/专利权人 CIBA-GEIGY AG;

    申请/专利号CH19720005406

  • 发明设计人 ROSSIALBERTODR.;

    申请日1968-10-25

  • 分类号C07C67/00;C07C69/76;

  • 国家 CH

  • 入库时间 2022-08-23 08:38:49

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