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still for framstellning new hydrogenated benzo (f) isoindolinderivat with therapeutic properties.

机译:仍用于frastelling具有治疗性能的新型氢化苯并(f)异吲哚酚。

摘要

1449159 Benzisoindoline derivatives SANDOZ Ltd 28 Sept 1973 [29 Sept 1972 3 Aug 1973] 45477/73 Heading C2C The invention comprises compounds of formula and their acid addition salts, wherein R is H, alkenyl or alkynyl, or alkyl optionally substituted by OH cycloalkyl, Ph (possibly monohalogen, alkyl or alkoxy substituted) or COZ: Z is OH, alkyl, alkoxy, Ph or halophenyl; R 1 , R 2 are each H, halogen or alkyl; and either X=Y=H and rings B and C are in cis-configuration, or X-Y forms an additional bond. In examples, these compounds are prepared by (a) epimerization, (b) N-substitution, (c) reduction or hydrolysis of an N-acyl analogue (A), (d) hydrogenolysis of an N-benzyl compound, (e) reduction of the compound in which X-Y forms a bond, (f) reduction of the 1,3- dioxo analogue (itself derived by dehydrating the tetrahydro - 1,3 - dioxo - 4 - hydroxy - 4- phenylbenzoisoindoline. Compounds (A) may be prepared by cyclizing (e.g.) an appropriate N,N - bis - cinnamyl- or N - cinnamyl - N- phenylpropynyl derivative of CF 3 CONH 2 . Therapeutic compositions, preferably administered orally, comprise compounds of the above formula, which have antidepressant and analgesic activity.
机译:1449159苯并异吲哚啉衍生物SANDOZ Ltd 1973年9月28日[1972年9月29日1973年8月3日] 45477/73标题C2C本发明包括下式的化合物及其酸加成盐,其中R为H,烯基或炔基或任选被OH环烷基取代的烷基, Ph(可能被单卤素,烷基或烷氧基取代)或COZ:Z为OH,烷基,烷氧基,Ph或卤代苯基; R 1,R 2分别为H,卤素或烷基; X = Y = H且环B和C处于顺式构型,或X-Y形成另一个键。在实例中,这些化合物通过(a)差向异构化,(b)N-取代,(c)N-酰基类似物(A)的还原或水解,(d)N-苄基化合物的氢解,(e)制备。还原其中XY形成键的化合物;(f)还原1,3-二氧代类似物(本身是通过脱水四氢-1,3-二氧代-4-羟基-4-苯基苯并异吲哚啉而得到的。)可以通过环化(例如)CF 3 CONH 2的合适的N,N-双-肉桂基-或N-肉桂基-N-苯基丙炔基衍生物来制备,优选口服施用的治疗组合物包含上式的化合物,其具有抗抑郁药和镇痛作用。

著录项

  • 公开/公告号SE394110B

    专利类型

  • 公开/公告日1977-06-06

    原文格式PDF

  • 申请/专利权人 SANDOZ AG;

    申请/专利号SE19730012916

  • 发明设计人 ACHINI R;OPPOLZER W;PFENNINGER E;

    申请日1973-09-21

  • 分类号C07D209/62;

  • 国家 SE

  • 入库时间 2022-08-23 00:43:01

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