首页> 外国专利> METHOD FOR SYNTHESIZING MEDICAL INTERMEDIATE PHENANTHRENE COMPOUNDS IN SODIUM ACETATE ENVIRONMENT

METHOD FOR SYNTHESIZING MEDICAL INTERMEDIATE PHENANTHRENE COMPOUNDS IN SODIUM ACETATE ENVIRONMENT

机译:醋酸钠环境中医药中间体菲化合物的合成方法

摘要

The present invention relates to a method for synthesizing medical intermediate phenanthrene compounds, as shown by formula (I) below, in a sodium acetate environment. The method comprises the following steps: reacting a compound as shown by formula (II) and a compound as shown by formula (III) in a solvent under an inert atmosphere in the presence of a catalyst, an organic ligand and sodium acetate, and thereby obtaining the compound of formula (I), wherein R1 and R2 are each independently H, C1-C6 alkyl, C1-C6 alkyloxy or halogen; and R3 is C6-C10 aryl or C5-C8 heteroaryl, wherein the C6-C10 aryl or C5-C8 heteroaryl is optionally substituted by 1-3 substituents, the substituents being C1-C6 alkyl or halogen. The method achieves good effects due to the selection of a suitable catalyst, organic ligand, base and solvent, and has wide industrial application prospects.
机译:本发明涉及在乙酸钠环境中合成如下式(I)所示的医学中间体菲化合物的方法。该方法包括以下步骤:在惰性气氛下,在催化剂,有机配体和乙酸钠存在下,使式(II)所示的化合物与式(III)所示的化合物在溶剂中反应,从而得到式(I)的化合物,其中R 1 和R 2 分别独立地为H,C 1 -C 6 < / Sub>烷基,C 1 -C 6 烷氧基或卤素;并且R 3 是C 6 -C 10 芳基或C 5 -C 8 杂芳基,其中C 6 -C 10 芳基或C 5 -C 8 杂芳基任选被1-3个取代基,取代基为C 1 -C 6 烷基或卤素。由于选择了合适的催化剂,有机配体,碱和溶剂,该方法取得了良好的效果,具有广阔的工业应用前景。

著录项

  • 公开/公告号WO2016141824A1

    专利类型

  • 公开/公告日2016-09-15

    原文格式PDF

  • 申请/专利权人 JIN YINGHUA;

    申请/专利号WO2016CN75401

  • 发明设计人 ZHAI XUEYAN;

    申请日2016-03-03

  • 分类号C07B37/10;C07C17/275;C07C2/42;C07C25/22;C07C15/30;C07D213/127;C07D213/16;

  • 国家 WO

  • 入库时间 2022-08-21 14:16:40

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