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N- Synthesis method of pyridine derivative through N-annulation reaction

机译:N-N环化反应合成吡啶衍生物的方法

摘要

The present invention provides a novel method for the easy, simple and efficient synthesis of various types of pyridine derivatives through an N-cyclization reaction under an organic catalyst. This synthesis method can be carried out without introducing the functional ps of oximes, imines or azides which have been conventionally used for the production of pyridine, but it is possible to use , -unsaturated aldehyde compound, ammonium acetate And a ketone compound to easily and simply provide various types of pyridine derivatives. The pyridine derivatives prepared by this synthesis method are very useful technologies widely applicable to the synthesis of pharmaceutical intermediates, natural products, agricultural chemicals, dyes, and electronic materials.
机译:本发明提供了一种在有机催化剂下通过N-环化反应容易,简单和有效地合成各种类型的吡啶衍生物的新颖方法。可以不引入通常用于生产吡啶的肟,亚胺或叠氮化物的官能团ps来进行该合成方法,但是可以使用不饱和醛化合物,乙酸铵和酮化合物容易地和简单地提供各种类型的吡啶衍生物。通过这种合成方法制备的吡啶衍生物是非常有用的技术,广泛适用于合成药物中间体,天然产物,农药,染料和电子材料。

著录项

  • 公开/公告号KR101806638B1

    专利类型

  • 公开/公告日2017-12-08

    原文格式PDF

  • 申请/专利权人 영남대학교 산학협력단;

    申请/专利号KR20150178282

  • 发明设计人 이용록;

    申请日2015-12-14

  • 分类号C07D213/02;B01J31/02;C07D213/06;C07D401/04;C07D405/04;

  • 国家 KR

  • 入库时间 2022-08-21 12:41:30

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