首页> 外国专利> Preparation method of AAA - trifluoro (Aminoacid (Gly and Na SALT) RIL) or a Straight arilcarboxilico ethanols acid, and their Addition salts with mineral acid or organic

Preparation method of AAA - trifluoro (Aminoacid (Gly and Na SALT) RIL) or a Straight arilcarboxilico ethanols acid, and their Addition salts with mineral acid or organic

机译:AAA-三氟(氨基酸(Gly和Na SALT)RIL)或直链阿立羧甲乙醇酸及其与无机酸或有机酸加成盐的制备方法

摘要

Procedure to obtain the TRIFLUORIDE (Alpha Alpha Alpha - amino aryl) or a Straight arilcarboxilico ethanols acid and its Salts addition of Mineral acid or Organic.It consists of the following steps: 1) condensation of an Amine (i) (Z alcoilo Hydrogen radical, radical cicloalcoilo, N - or N - alcoil piperidino aralcoilpiperidino; and Z represents a hydrogen or 'radical alcoilo bottom) with an H - tlorcarilcetona formula F AR co - Cf3; you get a P - amino arilcetona.2) reduction of the product to obtain the ariletanol sulfidation of the compound obtained, either for a tiocetona in ETHANETHIOL is reduced through an agent of hydrogenation. Optionally salifican (ii) compounds obtained by the addition of a Mineral acid or Organic. Antiinflammatory, antipyretic Analgesics. * * formula
机译:制备三氟甲烷(Alpha Alpha Alpha-氨基芳基)或直链芳烃羧酸的酸及其无机盐或有机盐的添加步骤,包括以下步骤:1)胺(i)(Z alcoilo氢自由基)的缩合;自由基基氯洛库洛基,N-或N-铝哌啶子基aralcoilpiperidino;和Z代表氢或“自由基的醇底”,其H-叔丁烯酮式为F AR co-Cf3; 2)产物的还原以获得所得到的化合物的芳醇的硫化,或者通过氢化剂将乙硫醇中的噻菌酮还原。任选地,通过添加无机酸或有机物获得的盐(ii)化合物。抗炎,解热镇痛药。 * *公式

著录项

  • 公开/公告号ES8101538A1

    专利类型

  • 公开/公告日1981-03-16

    原文格式PDF

  • 申请/专利号ES19790485656

  • 发明设计人

    申请日1979-11-02

  • 分类号C07C91/40;C07C103/00;C07C149/24;C07D295/04;

  • 国家 ES

  • 入库时间 2022-08-22 15:49:41

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