首页> 外国专利> A process for the preparation of compounds derived from 2.5 - is - 4 - hydroxy - azahexano; Intermediate imino Hydrazone and Nitrile, Nitrile, and processes to prepare such Intermediates.And imino Hydrazone

A process for the preparation of compounds derived from 2.5 - is - 4 - hydroxy - azahexano; Intermediate imino Hydrazone and Nitrile, Nitrile, and processes to prepare such Intermediates.And imino Hydrazone

机译:制备衍生自2.5- [is] -4-羟基-氮杂己基的化合物的方法;亚氨基Hy和丁腈中间体,以及制备此类中间体的工艺。

摘要

Describes a process for the preparation of compounds derived from 2.5 - [] - 4 - hydroxy azahexano diamine of formula (i),Where R1 is Hydrogen or a grupoamino protector suitable alkyl; R2 is replaced or not replaced; R3 is Hydrogen, alkyl, aryl, heterociclilo, replaced or not replaced,Ocicloalquil replaced or not replaced regardless of R1, R4,Amino Group is a hydrogen or adequate Protective and M is a number from 1 to 7 may be present; and where other Protecting groups suitable for functional groupsWhich compounds are active substances can antiviralmente or pharmaceutically Active emplearsecomo initial Compounds, in particular the antivirals.The precursor is a compound oxoThat in turn espreparado by hydrogenation with HYDRIDE or a suitable Compound with Hydrogen in the presence of a suitable Catalyst and Migration from an acyl Hydrazone toTime is preferably a nitrilovia imino Compound by means of hydrogenation reaction with Hydrazine and derivadode which is prepared by reaction of an aldehyde with a DriftOJ Reagent of a carboxylic acid in the presence of a Salt of cyanide; compuestosintermedios required for this; and processes for preparing such Intermediates.
机译:描述了由式(i)的2.5-[]-4-羟基氮杂己二胺衍生的化合物的制备方法,其中R 1为氢或适合于古鲁氨基保护基的烷基; R2已更换或未更换; R 3为氢,烷基,芳基,杂环基,被取代或未被取代;环氯喹被取代或未被取代,而与R 1,R 4无关,氨基为氢或足够的保护基,M为1至7的数字;以及其中适合于官能团的其他保护基团是活性物质的那些化合物,可以是抗病毒药或药学上具有活性的emplearsecomo初始化合物,特别是抗病毒药。合适的催化剂和从酰基Hy到时间的迁移优选为亚硝基亚氨基亚氨基化合物,其通过与肼和衍生基的加氢反应而进行,其是通过醛与羧酸的DriftOJ试剂在氰化物盐的存在下反应制备的。为此需要compuestosintermedios;以及制备此类中间体的过程。

著录项

  • 公开/公告号AR007290A1

    专利类型

  • 公开/公告日1999-10-27

    原文格式PDF

  • 申请/专利权人 NOVARTIS AG.;

    申请/专利号AR1997P102232

  • 发明设计人

    申请日1997-05-26

  • 分类号C07C213/08;C07C213/06;C07C215/20;C07C241/02;C07C253/16;C07C255/44;C07C281/02;C07C281/04;C07D207/02;C07D211/04;C07D213/42;C07D213/44;C07D213/54;C07D213/55;C07D257/02;C07D257/04;C07D275/02;C07D277/04;C07D277/08;C07D277/22;C07D277/30;C07D295/02;

  • 国家 AR

  • 入库时间 2022-08-22 02:28:24

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