首页> 外国专利> METHOD OF SYNTHESIZING PHARMACEUTICAL INTERMEDIATE PHENANTHRENE COMPOUND IN THE PRESENCE OF DIISOPROPYLAMINE

METHOD OF SYNTHESIZING PHARMACEUTICAL INTERMEDIATE PHENANTHRENE COMPOUND IN THE PRESENCE OF DIISOPROPYLAMINE

机译:二异丙基丙胺存在下的药物中间体菲化合物的合成方法

摘要

The present invention relates to a method of synthesizing a phenanthrene compound, represented by formula (I), in the presence of a diisopropylamine. The method comprises: in an inert atmosphere, and in the presence of a catalyst, an organic ligand, and a diisopropylamine, reacting in a solvent a compound represented by formula (II) and a compound represented by formula (III) to obtain a compound represented by formula (I), wherein R1 and R2 are independently an H, a C1-C6 alkyl, a C1-C6 alkyloxy or a halogen; R3 is a C6-C10 aryl or a C5-C8 heteroaryl; the C6-C10 aryl or the C5-C8 heteroaryl is optionally substituted with 1-3 substituent groups; and the substituent groups are a C1-C6 alkyl or a halogen. The method obtains a favorable result by selecting a suitable catalyst, an organic ligand, a base, and a solvent, and has a wide prospect for an industrial application.
机译:本发明涉及在二异丙胺存在下合成式(I)表示的菲化合物的方法。该方法包括:在惰性气氛中,在催化剂,有机配体和二异丙基胺的存在下,在溶剂中使由式(II)表示的化合物和由式(III)表示的化合物反应以获得化合物。由式(I)表示的化合物,其中R 1和R 2独立地为H,C 1 -C 6烷基,C 1 -C 6烷氧基或卤素; R3为C6-C10芳基或C5-C8杂芳基; C6-C10芳基或C5-C8杂芳基任选被1-3个取代基取代。取代基为碳数1〜6的烷基或卤素。通过选择合适的催化剂,有机配体,碱和溶剂,该方法获得了良好的结果,在工业上具有广阔的前景。

著录项

  • 公开/公告号WO2016141827A1

    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WO2016CN75404

  • 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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