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Cyanpropene derivatives for single drug preparation, single drug preparation, containing ingredients and processes to produce single drug preparation

机译:用于单一药物制剂,单一药物制剂的氰基丙烯衍生物,包含其成分和制备单一药物制剂的方法

摘要

1. A formula compound I, wherein R1 is halogenated, hydroxy, alcox C1-C5, C1-C5 tar, R2 is h, halogenated, hydroxy, alcox C1-C5, and R3 and R4 are h, halogenated, hydroxy, alcox C1-C5, X is O, s, es-cr5r6 -;R5 and R6 are h, halogen, C1-C10 tar substitutes or non substitutes respectively; W is h, the acidity produced by naturally occurring amino acid derivatives; Z is h, C1-C10 tar substitutes or non halogen substitutes, C1-C5 hydroxide compounds, etc. The preferred compound is benzoate (2S, 4S) - 2-cyano-4-fluoro-1 - [(2-hydroxy-1, 1-dimethyl) acetylpyridine. A pharmacological component is also mentioned, which contains a stabilizer selected between sugar and sugar alcohol, reducing the decomposition of the compound,And a preparation procedure. These compounds are the fourth (DPIV) effective inhibitors for the treatment of type 2 diabetes.
机译:1.一种式I的化合物,其中R 1为卤代的,羟基的,醇C 1 -C 5,C 1 -C 5焦油,R 2为h,卤代的,羟基,醇C 1 -C 5,R 3和R 4为h,卤代的羟基,醇,C 1 -C5,X为O,s,es-cr5r6--; R5和R6分别为h,卤素,C1-C10焦油取代基或非取代基; W是h,天然氨基酸衍生物产生的酸度; Z为h,C1-C10焦油取代基或非卤素取代基,C1-C5氢氧化物等。优选的化合物为苯甲酸酯(2S,4S)-2-氰基-4-氟-1-[[(2-羟基-1) ,1-二甲基)乙酰基吡啶。还提到了药理成分,其包含在糖和糖醇之间选择的稳定剂,减少了化合物的分解,以及制备方法。这些化合物是用于治疗2型糖尿病的第四种(DPIV)有效抑制剂。

著录项

  • 公开/公告号PE20061199A1

    专利类型

  • 公开/公告日2006-11-18

    原文格式PDF

  • 申请/专利权人 TAISHO PHARMACEUTICAL CO. LTD.;

    申请/专利号PE20030200600

  • 发明设计人 YAZAKI HIROAKI;IKUTA HIROSHI;

    申请日2006-01-24

  • 分类号A61K31/40;A61K47/10;A61K47/26;A61P3/10;

  • 国家 PE

  • 入库时间 2022-08-21 20:56:44

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