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New synthetic intermediate field and its production method of karubapenemu chemical compound for oral administration

机译:氨基甲酸酯类化合物的合成新中间体领域及其生产方法

摘要

This invention offers the new synthetic intermediate field and its production method in order to produce the 1- mechirukarubapenemu chemical compound for oral administration efficiently. In other words, this invention is displayed with general system it is production method of the new - lactam compound which (3) the new - lactam compound which (1) makes the new - lactam compound which (6) reacts under existing of chemical compound and the base which (5) designates the - lactam compound which as the starting raw materials, are displayed with general system is displayed with, general system after protecting hydroxyl group, is displayed with general system profit, features that this is protected deviation from the cyclization point strongly under existing of the base, furthermore by reacting with chloridation diphenyl phosphoric acid, is displayed with general system (4).(In formula, R1: torimechirushiriru basis or toriechirushiriru basis, R2: Aryl basis or hetero aryl basis, R3: Carbon count alkyl group or carbon count shikuroarukiru 3 of 1 - 10 - 10, X: The halogen atom is shown)
机译:本发明提供了一种新的合成中间体领域及其生产方法,以有效地生产用于口服的1-甲卡鲁卡波拉彭尼姆化合物。换句话说,本发明以通用体系展示为新的内酰胺化合物的制造方法,其中,(3)在化合物的存在下使(1)的新的内酰胺化合物与(6)反应的新的内酰胺化合物进行反应。 (5)表示作为起始原料的-内酰胺化合物的碱,以一般体系显示,以保护羟基后的一般体系显示,以一般系统利润显示,这是受保护的偏离通式(4)表示在碱的存在下强烈存在下的环化点,此外还与氯化二苯基磷酸反应得到环化点。 > 2 :芳基或杂芳基,R 3 :碳数烷基或碳数shikuroarukiru 3 of 1-10-10,X:显示卤原子)

著录项

  • 公开/公告号JPWO2004043973A1

    专利类型

  • 公开/公告日2006-03-09

    原文格式PDF

  • 申请/专利权人 株式会社カネカ;

    申请/专利号JP20040551226

  • 发明设计人 西野 敬太;古賀 照義;

    申请日2003-11-13

  • 分类号C07F9/6561;C07F19/00;C07D205/08;C07B61/00;

  • 国家 JP

  • 入库时间 2022-08-21 21:48:41

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