首页> 外国专利> Preparation method of (3-chloro-4-fluorophenyl) - (4 - (5 fluoro - 4 - methyl - 2 - methyl - pyrimidin-2-yl) - amino methyl - piperidin-1-yl) - methanone Derivatives of pyrimidine compounds and Intermediates

Preparation method of (3-chloro-4-fluorophenyl) - (4 - (5 fluoro - 4 - methyl - 2 - methyl - pyrimidin-2-yl) - amino methyl - piperidin-1-yl) - methanone Derivatives of pyrimidine compounds and Intermediates

机译:(3-氯-4-氟苯基)-(4-[[((5-氟-4-甲基-2-甲基-嘧啶-2-基)-氨基]甲基]-哌啶-1-基)-甲酮的制备方法嘧啶化合物及其中间体的衍生物

摘要

This is a method to prepare (3-chloro-4-fluorophenyl) - ((4 - (4 - [(fluoro - 5 - methyl - 2 - methyl - pyrimidin-2-yl) - amino] - amino] methyl} - piperidin-1-yl) - methanone, formula (1), condensation between 5 - methyl - 2 - methylamine pyrimidine of formula (2), and cyanohydrin of formula (3). Claim 1: 5 - methyl - 2 - amino pyrimidine of formula (2).Claim 1: The pyrimidine Derivatives of formula (4), where the Radicals R1 and R2 independently represent a hydrogen Atom or a group or a Group benciloxicarbonilo tert butiloxicarbonilo; where R1 and R2 together with the atom of nitrogen Carrier form a phthalimido Group. Claim 1: The pyrimidine Derivatives of formula (5) to (7).
机译:这是一种制备(3-氯-4-氟苯基)-((4​​-(4-[(氟-5-甲基-2-甲基-嘧啶-2-基)-氨基]-氨基]甲基}-权利要求1:式(1)的5-甲基-2-氨基嘧啶:式(1)的哌啶-1-基)-甲酮,式(2)的5-甲基-2-甲胺嘧啶与式(3)的氰醇缩合。权利要求1:式(4)的嘧啶衍生物,其中基团R1和R2独立地代表氢原子或一个基团或一个基团;或其中R1和R2与氮原子一起形成载体形式权利要求1的式(5)至(7)的嘧啶衍生物。

著录项

  • 公开/公告号AR056543A1

    专利类型

  • 公开/公告日2007-10-10

    原文格式PDF

  • 申请/专利权人 PIERRE FABRE MEDICAMENT;

    申请/专利号AR2006P104233

  • 发明设计人

    申请日2006-09-27

  • 分类号C07D401/12;C07D239/26;C07D403/06;

  • 国家 AR

  • 入库时间 2022-08-21 20:59:35

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