首页> 外国专利> METHOD FOR SYNTHESISING PHARMACEUTICAL INTERMEDIATE PHENANTHRENE COMPOUND IN POTASSIUM TERT-BUTOXIDE ENVIRONMENT

METHOD FOR SYNTHESISING PHARMACEUTICAL INTERMEDIATE PHENANTHRENE COMPOUND IN POTASSIUM TERT-BUTOXIDE ENVIRONMENT

机译:叔丁基溴化钾环境中药物中间体菲的合成方法

摘要

The present invention relates to a method for synthesising a phenanthrene compound as shown in formula (I) in a potassium tert-butoxide environment, the method comprising: reacting the compound of formula (II) with the compound of formula (III) in an inert atmosphere, in the presence of a catalyst, organic ligands and potassium tert-butoxide, and in a solvent, thereby obtaining the compound of formula (I), wherein R1 and R2 are each independently H, a C1-C6 alkyl group, a C1-C6 alkoxy group or a halogen, R3 is a C6-C10 aryl group or a C5-C8 heteroaryl group, the C6-C10 aryl group or the C5-C8 heteroaryl group being optionally substituted by 1-3 substituents, the substituents being C1-C6 alkyl groups or halogens. The method obtains a good effect via the selection of an appropriate catalyst, organic ligands, base and solvent, and has wide prospects for industrial application.
机译:本发明涉及在叔丁醇钾环境中合成式(I)所示的菲化合物的方法,该方法包括:使式(II)的化合物与式(III)的化合物在惰性条件下反应。在大气中,在催化剂,有机配体和叔丁醇钾的存在下,在溶剂中,从而获得式(I)的化合物,其中R 1 和R 2 各自独立为H,C 1 -C 6 烷基,C 1 -C 6 烷氧基或卤素,R 3 是C 6 -C 10 芳基或C 5 - C 8 杂芳基,C 6 -C 10 芳基或C 5 -C 8 杂芳基可任选地被1-3个取代基取代,所述取代基为C 1 -C 6 烷基或卤素。通过选择合适的催化剂,有机配体,碱和溶剂,该方法效果良好,具有广阔的工业应用前景。

著录项

  • 公开/公告号WO2016141826A1

    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WO2016CN75403

  • 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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