首页> 外国专利> Process for preparing a formilfosfonico acid derivative, Process for preparing an Acid formilfosfonico,A Salt or hydrate thereof and process to prepare N - (PHOSPHONOMETHYL) glycine, or a Salt or Ester of the same

Process for preparing a formilfosfonico acid derivative, Process for preparing an Acid formilfosfonico,A Salt or hydrate thereof and process to prepare N - (PHOSPHONOMETHYL) glycine, or a Salt or Ester of the same

机译:制备福尔马芬酸衍生物的方法,制备福尔马芬酸的盐,其盐或水合物的方法以及制备N-(膦酰基)甘氨酸或其盐或酯的方法

摘要

It reveals a process for the preparation of acid formilfosfonico,And its derivatives where the process involves DECOMPOSING a compound oxide (PHOSPHONOMETHYL) Amine in the presence of a catalyst to produce the derivative decomposition deu00e1ci OJ formilfosfoniCo and an Amine desfosfonometilada.Serevela also a process for the preparation of acid formilfosfonico, wherein the process comprises oxidize nitrilotris or a Salt thereof to will become - nitrilotris oxide or Salt Law,N - oxide and decompose the nitrilotris or Salt thereof in the presence of a catalyst decomposition.Anotherimportant of This relates to a process for preparing N - (PHOSPHONOMETHYL) glycine, or a Salt or Ester thereof,Where comprendedescomponer Windows approach or an oxide Compound (PHOSPHONOMETHYL) Amine in the presence of a catalyst to produce a Derivative of acid decomposition formilfosfonicoy des amineFosfonometilada, and react to produce deu00e1cido formilfo sfonico derivative N - (PHOSPHONOMETHYL) glycine, or a Salt or an ester of the same.Of particular interest is a realization of this process in which the Reaction for producing N - (PHOSPHONOMETHYL glycine) is achieved by condensaciondelderivado acid F with a ormilfosfonico conTo reduce the product of Glycine, and condensed to produce N - (PHOSPHONOMETHYL glycine).Another aspect which is of particular interest is one in which the Derivative of formilfosfonico secondensa acid with 1 - amino - 2 - roxietano HID to produce a intermediarioalcoholico condensateThe intermediary alcoholic condensate is reduced to produce a compound N - (2 - hydroxyethyl) - N - (PHOSPHONOMETHYL) amineAnd the compuestoden - (2 - hydroxyethyl) - N - (PHOSPHONOMETHYL) Amine is oxidiza pa ra producing N - (PHOSPHONOMETHYL glycine).The formilfosfonico acid can be used as a precursor in the synthesis of N - (PHOSPHONOMETHYL glycine), a highly effective Commercial herbicide.The u00e1cidoformilfosfonico can alternatively be used as a ermediarioavanzado int in the preparation of compounds of medicinal importance such as an antiviral agent fosfonohidroxiac acidEthical.
机译:它揭示了一种制备米糠酚酸及其衍生物的方法,该方法包括在催化剂的存在下分解复合氧化物(膦酰基甲基)胺,以生成衍生物分解产物,从而制得米糠酚和胺胺。制备米糠草酸的方法,其中该方法包括在催化剂分解的存在下,氧化次氮基三醇或其盐,将其变成-次氮基三氧化物或盐定律,N-氧化物并分解次氮基三醇或其盐。本发明涉及制备N-(膦酰基)甘氨酸或其盐或酯的方法,其中,在催化剂的存在下,用componder Windows方法或氧化物化合物(PHOSPHOMEMETYL)胺来生产酸分解的衍生物,用于胺代膦酸酯和反应。产生de u00e1cido formilfo sfonico衍生物N-(膦酰基甲基)甘氨酸,特别令人感兴趣的是该方法的实现,其中用于生产N-的反应是通过缩合苯二酰derderivado酸F与有机锡化合物缩合来还原甘氨酸的产物,然后缩合为产生N-(膦酰基甲基甘氨酸)。另一个特别令人感兴趣的方面是其中甲磺酰福芬酸与1-氨基-2-罗希坦诺HID的衍生物可生成中间醇缩合物将中间醇缩合物还原以生成化合物N- (2-羟乙基)-N-(磷酸甲胺)胺和被缩合的-(2-羟乙基)-N-(磷酸甲胺)胺被氧化生成N-(磷酸甲氧甘氨酸)。合成高效商用除草剂N-(磷酸膦酸甘氨酸)。 u00e1cidoformilfosfonico也可以在制备前用作ermediarioavanzado int分离具有药用价值的化合物,例如抗病毒药膦磷酰氧己酸。

著录项

  • 公开/公告号AR021767A1

    专利类型

  • 公开/公告日2002-08-07

    原文格式PDF

  • 申请/专利权人 SABBA DA SILVA LIMA MICHELE;

    申请/专利号AR1999P104056

  • 发明设计人

    申请日1999-08-12

  • 分类号C07C309/04;

  • 国家 AR

  • 入库时间 2022-08-22 00:46:26

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