首页> 外国专利> New derivatives of the 20,21 - dinoreburnamenine substituted in 15 by an amine group, their process of preparation and # # thus obtained, their application as medicinal products and the pharmaceutical compositions the reenfermant

New derivatives of the 20,21 - dinoreburnamenine substituted in 15 by an amine group, their process of preparation and # # thus obtained, their application as medicinal products and the pharmaceutical compositions the reenfermant

机译:在15中被一个胺基取代的20,21-dinoreburnamenine的新衍生物,其制备方法和由此获得的##,作为医药产品的用途和药物组合物

摘要

PCT No. PCT/FR89/00335 Sec. 371 Date Feb. 23, 1990 Sec. 102(e) Date Feb. 23, 1990 PCT Filed Jun. 28, 1989 PCT Pub. No. WO90/00171 PCT Pub. Date Jan. 11, 1990.A compound selected from the group consisting of a compound of the formula (I): IMAGE in which R1 and R2 are individually selected from the group consisting of hydrogen, an alkyl of 1 to 5 carbon atoms, -(CH2)n-OH in which n is between 2 and 5, an aryl or arylalkyl of 7 to 12 carbon atoms, these two radicals being optionally substituted, IMAGE in which R3 is an alkyl of 7 to 12 carbon atoms, these two radicals being optionally substituted, with the proviso that R1 and R2 are not both aryl simultaneously, or R1 and R2 form, together with the nitrogen atom to which they are linked, a saturated or unsaturated heterocyclic which can contain a second heteroatom chosen from oxygen, sulphur and nitrogen optionally substituted by an alkyl of 1 to 5 carbon atoms, aryl, arylalkyl of 7 to 12 carbon atoms, these radicals being optionally substituted, R4 and R5 are individually selected from the group consisting of hydrogen, halogen, alkyl or alkoxy of 1 to 5 carbon atoms, hydroxy, trifluoromethyl or nitro, the said products of formula (I) being in all the possible enantiomeric and diastereoisomeric forms and its non-toxic, pharmaceutically acceptable acid addition salts having an excellent analgesic activity.
机译:PCT号PCT / FR89 / 00335第二部分371日期1990年2月23日,秒102(e),1990年2月23日,PCT,1989年6月28日提交,PCT Pub。 WO90 / 00171 PCT公开号1990年1月11日发布,该化合物选自式(I)的化合物:其中R1和R2分别选自氢,1-5个碳原子的烷基,-(CH 2)n -OH,其中n在2至5之间,具有7至12个碳原子的芳基或芳基烷基,这两个基团是任选取代的,,其中R 3是具有7至12个碳原子的烷基,这两个基团可以任选地被取代,条件是R1和R2不能同时为芳基,或者R1和R2与它们所连接的氮原子一起形成饱和或不饱和杂环,可以包含选择的第二个杂原子选自氧,硫和氮,其任选地被1至5个碳原子的烷基,芳基,7至12个碳原子的芳基烷基取代,这些基团是任选取代的,R4和R5分别选自氢,卤素,烷基或1至5个碳原子的烷氧基,羟基,三氟甲基或硝基,所述式(I)的产物为所有可能的对映异构和非对映异构形式,并且其无毒的药学上可接受的酸加成盐具有优异的镇痛活性。

著录项

  • 公开/公告号GR3006582T3

    专利类型

  • 公开/公告日1993-06-30

    原文格式PDF

  • 申请/专利权人

    申请/专利号GR19920402523T

  • 发明设计人

    申请日1992-12-18

  • 分类号A61K31/435;A61P25/04;C07D461;

  • 国家 GR

  • 入库时间 2022-08-22 05:11:44

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