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new type prostaglandin compound, their preparation and medicines containing plant

机译:新型前列腺素化合物及其制剂和含植物的药物

摘要

13,14-Dihydro-15-methyl-prostaglandin derivatives of the formula IMAGE in which M is one of the two groups IMAGE or IMAGE, g is 3, 4 or 5 and n is 2 to 6, as well as mixtures of this compound and the enantiomer thereof, are prepared by acylating all hydroxyl groups of an optically active lactone or a mixture of this lactone and the enantiomer thereof and then separating the resulting epimer mixture chromatographically. Thereafter, the acyl groups are again removed by hydrolysis and the double bond present is hydrogenated. Finally, the product is reduced to the corresponding lactol and the side chain is introduced into the latter by reaction with a Wittig reagent. The free acid obtained is also esterified to give esters. Further, the resulting PFG-like compound is converted to a PGE-like compound, a PGA-like compound or a PGB-like compound. The compounds obtained, as well as their salts and esters, can be used for the same pharmacological purposes as corresponding known prostaglandin derivatives.
机译:的13,14-二氢-15-甲基-前列腺素衍生物,其中M为两个组之一,g为3、4或5,n为2至6,如通过酰化旋光内酯的所有羟基或该内酯及其对映异构体的混合物的所有羟基,然后色谱分离得到的差向异构体混合物,可制备该化合物及其对映异构体的混合物。此后,再次通过水解除去酰基并将存在的双键氢化。最后,将产物还原为相应的内酯,并通过与维蒂希试剂反应将侧链引入后​​者。所得的游离酸也被酯化得到酯。此外,将所得的PFG状化合物转化为PGE状化合物,PGA状化合物或PGB状化合物。所获得的化合物及其盐和酯可与相应的已知前列腺素衍生物用于相同的药理学目的。

著录项

  • 公开/公告号BE841056A

    专利类型

  • 公开/公告日1976-10-25

    原文格式PDF

  • 申请/专利权人

    申请/专利号BE19760166402

  • 发明设计人

    申请日1976-04-23

  • 分类号C07C;

  • 国家 BE

  • 入库时间 2022-08-23 02:59:07

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