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(4-chloro-5-trifluoromethyl-pyrimidin-2-yl)-cyclohexylamine | 847863-15-4

中文名称
——
中文别名
——
英文名称
(4-chloro-5-trifluoromethyl-pyrimidin-2-yl)-cyclohexylamine
英文别名
4-chloro-N-cyclohexyl-5-(trifluoromethyl)pyrimidin-2-amine
(4-chloro-5-trifluoromethyl-pyrimidin-2-yl)-cyclohexylamine化学式
CAS
847863-15-4
化学式
C11H13ClF3N3
mdl
——
分子量
279.693
InChiKey
FBYNXPUIAGSSRB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    37.8
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Selective addition of amines to 5-trifluoromethyl-2,4-dichloropyrimidine induced by Lewis acids
    摘要:
    A variety of 2,4-diamino-pyrimidine systems can be prepared from the corresponding 2,4-dichloropyrimidine by sequential addition of two amines, the first adding selectively to the 4-position. In contrast it was found that 2,4-dichloro-5-trifluoromethyl-pyrimidine yields a 1:1 mixture of the two possible isomers. Lewis acids were employed to increase the ratio of isomers to >10:1 in favor of the 2-addition product. Optimization of the effect of Lewis acid additives on this and other dichloropyrimidine systems will be discussed. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.025
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文献信息

  • [EN] SELECTIVE SYNTHESIS OF CF3-SUBSTITUTED PYRIMIDINES<br/>[FR] SYNTHÈSE SÉLECTIVE DE PYRIMIDINES SUBSTITUÉES EN CF3
    申请人:PFIZER PROD INC
    公开号:WO2005023780A1
    公开(公告)日:2005-03-17
    The present invention relates to a method of making a compound of the formula (I),wherein X1, X2 and R3-R4 are as defined herein. The method includes reacting a compound of the formula (II) with an amine of formula (III) (HNR3R4) in the presence of a Lewis Acid and a non-nucleophilic base. The 2,4-diamino pyrimidine moiety is a common component in a variety of biologically active drug-like molecules and pyrimidine derivatives have been found to be useful in the 10 treatment of abnormal cell growth, such as cancer, in mammals.
    本发明涉及一种制备公式(I)化合物的方法,其中X1、X2和R3-R4如本文所定义。该方法包括在路易斯酸和非亲核碱存在下,将公式(II)化合物与公式(III)胺(HNR3R4)反应。2,4-二氨基嘧啶基团是各种生物活性类药物分子中的常见组分,已发现嘧啶衍生物在哺乳动物的异常细胞生长治疗中很有用,例如癌症治疗。
  • Selective synthesis of CF3-substituted pyrimidines
    申请人:Kath Charles John
    公开号:US20050101620A1
    公开(公告)日:2005-05-12
    The present invention relates to a method of making a compound of the formula wherein X 1 , X 2 and R 3 —R 4 are as defined herein. The method includes reacting a compound of the formula with an amine of formula 3 (HNR 3 R 4 ) in the presence of a Lewis Acid and a non-nucleophilic base. The 2,4-diamino pyrimidine moiety is a common component in a variety of biologically active drug-like molecules and pyrimidine derivatives have been found to be useful in the treatment of abnormal cell growth, such as cancer, in mammals.
    本发明涉及一种制备化合物的方法,该化合物的结构式为其中X1,X2和R3-R4如定义所示。该方法包括在路易斯酸和非亲核碱存在下,将式化合物与式3的胺反应。2,4-二氨基嘧啶基团是各种生物活性药物分子中的常见组成部分,已发现嘧啶衍生物在治疗哺乳动物异常细胞生长(如癌症)方面非常有用。
  • SELECTIVE SYNTHESIS OF CF3-SUBSTITUTED PYRIMIDINES
    申请人:Pfizer Products Inc.
    公开号:EP1663991B1
    公开(公告)日:2007-01-10
  • US7122670B2
    申请人:——
    公开号:US7122670B2
    公开(公告)日:2006-10-17
  • Selective addition of amines to 5-trifluoromethyl-2,4-dichloropyrimidine induced by Lewis acids
    作者:Daniel T. Richter、John C. Kath、Michael J. Luzzio、Nandell Keene、Martin A. Berliner、Matthew D. Wessel
    DOI:10.1016/j.tetlet.2013.06.025
    日期:2013.8
    A variety of 2,4-diamino-pyrimidine systems can be prepared from the corresponding 2,4-dichloropyrimidine by sequential addition of two amines, the first adding selectively to the 4-position. In contrast it was found that 2,4-dichloro-5-trifluoromethyl-pyrimidine yields a 1:1 mixture of the two possible isomers. Lewis acids were employed to increase the ratio of isomers to >10:1 in favor of the 2-addition product. Optimization of the effect of Lewis acid additives on this and other dichloropyrimidine systems will be discussed. (C) 2013 Elsevier Ltd. All rights reserved.
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