where values R1 and R2 are given in p. 1 of the invention claim. Method involves the synthesis of boronic acid derivative followed by its coupling with the compound of the formula X-C6H4-R2 where X means bromine or iodine atoms and R2 means H, OH or OR4 where R4 means hydroxy-protective group. Synthesized compound can be used as an intermediate substance for synthesis of pharmaceutically active compounds being others are useful for treatment of women with osteoporosis in the phase of postmenopause. EFFECT: simplified and decreased cost of process. 32 cl, 1 dwg, 3 ex"/> METHOD OF SYNTHESIS OF 2-SUBSTITUTED BENZOBTHIOPHENE (VARIANTS), METHOD OF SYNTHESIS OF DERIVATIVES OF 2-PHENYL-3-AROYLBENZOBTHIOPHENE (VARIANTS) AND DERIVATIVES OF BENZOBTHIOPHENE
首页> 外国专利> METHOD OF SYNTHESIS OF 2-SUBSTITUTED BENZOBTHIOPHENE (VARIANTS), METHOD OF SYNTHESIS OF DERIVATIVES OF 2-PHENYL-3-AROYLBENZOBTHIOPHENE (VARIANTS) AND DERIVATIVES OF BENZOBTHIOPHENE

METHOD OF SYNTHESIS OF 2-SUBSTITUTED BENZOBTHIOPHENE (VARIANTS), METHOD OF SYNTHESIS OF DERIVATIVES OF 2-PHENYL-3-AROYLBENZOBTHIOPHENE (VARIANTS) AND DERIVATIVES OF BENZOBTHIOPHENE

机译:2-取代的苯并[B]噻吩(衍生物)的合成方法,2-苯基-3-芳基苯并[B]噻吩(衍生物)的衍生物和苯并[B]噻吩的衍生物的合成方法

摘要

FIELD: organic chemistry, pharmacy, chemical technology. SUBSTANCE: invention describes the method of synthesis of the novel 2-substituted benzo[b] thiophene of the general formula (I) where values R1 and R2 are given in p. 1 of the invention claim. Method involves the synthesis of boronic acid derivative followed by its coupling with the compound of the formula X-C6H4-R2 where X means bromine or iodine atoms and R2 means H, OH or OR4 where R4 means hydroxy-protective group. Synthesized compound can be used as an intermediate substance for synthesis of pharmaceutically active compounds being others are useful for treatment of women with osteoporosis in the phase of postmenopause. EFFECT: simplified and decreased cost of process. 32 cl, 1 dwg, 3 ex
机译:领域:有机化学,制药,化学技术。物质:本发明描述了通式(I)的新型2-取代的苯并[b]噻吩的合成方法。<图像文件=“ 00000002.GIF” he =“ 24” id =“ imag0.2” imgContent =“ undefined“ imgFormat =” GIF“ wi =” 49“ />,其中p中给出了值R 1 和R 2 。本发明的权利要求1。方法包括合成硼酸衍生物,然后将其与式XC 6 H 4 -R 2 的化合物偶联,其中X表示溴或碘原子,R 2 表示H,OH或OR 4 ,其中R 4 表示羟基。合成的化合物可用作合成药物活性化合物的中间体,其他化合物也可用于治疗绝经后阶段的骨质疏松症妇女。效果:简化并降低了流程成本。 32 cl,1 dwg,3 ex

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