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4-甲基-6-吡啶-3-嘧啶-2-胺 | 90916-52-2

中文名称
4-甲基-6-吡啶-3-嘧啶-2-胺
中文别名
4-甲基-6-吡啶-3-基嘧啶-2-胺
英文名称
3-(2-amino-4-methylpyrimidin-6-yl)pyridine
英文别名
4-methyl-6-(pyridin-3-yl)pyrimidin-2-amine;4-methyl-6-pyridin-3-yl-pyrimidin-2-ylamine;4-methyl-6-pyridin-3-yl-pyrimidin-2-yl-amine;2-Amino-4-methyl-6-pyridin-3-yl>-pyrimidin;2-Amino-4-methyl-6-β-pyridyl-pyrimidin;2-Amino-4-methyl-6-pyridyl-(2)-pyrimidin;4-methyl-6-pyridin-3-ylpyrimidin-2-amine
4-甲基-6-吡啶-3-嘧啶-2-胺化学式
CAS
90916-52-2
化学式
C10H10N4
mdl
——
分子量
186.216
InChiKey
RUMJWDANHSNYCE-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):
    0.8
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    64.7
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933990090

SDS

SDS:96fb63a3bf7e6456609324a23e17a24b
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-甲基-6-吡啶-3-嘧啶-2-胺羟胺N,N-二异丙基乙胺 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇二甲基亚砜 为溶剂, 反应 22.0h, 生成
    参考文献:
    名称:
    CN116768854
    摘要:
    公开号:
  • 作为产物:
    描述:
    2-氨基-4-氯-6-甲基嘧啶3-吡啶硼酸 在 bis-triphenylphosphine-palladium(II) chloride sodium carbonate 作用下, 以 乙腈 为溶剂, 反应 7.0h, 以74%的产率得到4-甲基-6-吡啶-3-嘧啶-2-胺
    参考文献:
    名称:
    Synthesis of New N-Arylpyrimidin-2-amine Derivatives Using a Palladium Catalyst
    摘要:
    通过应用优化的Buchwald-Hartwig氨基化条件,使用二氯双(三苯基膦)钯(II)、xantphos和叔丁醇钠,在氮气氛围下于回流甲苯中,从相应的胺合成了新型N-芳基-4-(吡啶-3-基)嘧啶-2-胺衍生物。所得到的N-芳基衍生物产率从中等到良好,范围在27%至82%之间。描述的程序可广泛用于制备新型杂环化合物。新化合物的结构通过FT-NMR、FT-IR和元素分析得到了确认。
    DOI:
    10.3390/molecules13040818
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文献信息

  • Pyrimidine Derivatives As HSP90 Inhibitors
    申请人:Chessari Gianni
    公开号:US20090215777A1
    公开(公告)日:2009-08-27
    The invention provides a compound for use as an inhibitor of Hsp90, the compound having the formula (I): or salts, tautomers, solvates or N-oxides thereof; wherein: A is N or a group CR 3 ; R 1 is a monocyclic or bicyclic carbocyclic or heterocyclic ring of 5 to 10 ring members of which up to two ring members may be heteroatoms selected from N, O and S and the remainder are carbon atoms, the carbocyclic or heterocyclic ring being optionally substituted by one or more substituent groups independently selected from R 10 ; and R 2 , R 3 and R 10 are as defined in the claims.
    该发明提供了一种化合物,用作Hsp90的抑制剂,该化合物具有以下式(I):或其盐、互变异构体、溶剂合物或N-氧化物;其中:A为N或CR基团;R1为由5至10个环成员组成的单环或双环碳环或杂环,其中最多两个环成员可以是从N、O和S中选择的杂原子,其余为碳原子,碳环或杂环可以选择地被一个或多个取代基独立地选择自R10的取代基取代;而R2、R3和R10如权利要求中所定义。
  • Synthesis of New N-Arylpyrimidin-2-amine Derivatives Using a Palladium Catalyst
    作者:Ibrahim El-Deeb、Jae Ryu、So Lee
    DOI:10.3390/molecules13040818
    日期:——
    New N-aryl-4-(pyridin-3-yl)pyrimidin-2-amine derivatives were synthesizedfrom the corresponding amines, applying optimized Buchwald-Hartwig aminationconditions using dichlorobis(triphenylphosphine)Pd(II), xantphos and sodium tertbutoxidein refluxing toluene under a nitrogen atmosphere. The target N-aryl derivativeswere obtained in moderate to good yields ranging from 27% to 82%. The proceduredescribed could be widely employed for the preparation of new heterocyclic compounds.The structures of the new compounds were confirmed by FT-NMR, FT-IR and elementalanalysis.
    通过应用优化的Buchwald-Hartwig氨基化条件,使用二氯双(三苯基膦)钯(II)、xantphos和叔丁醇钠,在氮气氛围下于回流甲苯中,从相应的胺合成了新型N-芳基-4-(吡啶-3-基)嘧啶-2-胺衍生物。所得到的N-芳基衍生物产率从中等到良好,范围在27%至82%之间。描述的程序可广泛用于制备新型杂环化合物。新化合物的结构通过FT-NMR、FT-IR和元素分析得到了确认。
  • Directed supramolecular assembly of Cu(<scp>ii</scp>)-based “paddlewheels” into infinite 1-D chains using structurally bifunctional ligands
    作者:Christer B. Aakeröy、Nate Schultheiss、John Desper
    DOI:10.1039/b513765a
    日期:——
    The construction of Cu(II)-containing supramolecular chains is achieved by combining suitable anionic ligands (for controlling the coordination geometry and for creating a neutral building block) with four new bifunctional ligands containing a metal-coordinating pyridyl site and a self-complementary hydrogen-bonding moiety. Seven crystal structures are presented and in each case, the copper(II) complex displays a “paddlewheel” arrangement, with four carboxylate ligands occupying the equatorial sites, leaving room for the bifunctional ligand to coordinate in the axial positions. The supramolecular chemistry, which organizes the coordination-complexes into the desired infinite 1-D chains, is driven by a combination of N–H⋯N and N–H⋯O hydrogen-bonds in five of the seven structures.
    通过将合适的阴离子配体(用于控制配位几何和创建中性构件)与四种新的双功能配体(包含一个金属配位吡啶基位点和一个自互补氢键分子)相结合,可以构建含铜(II)的超分子链。本文展示了七种晶体结构,每种情况下,铜(II)配合物都呈现 "桨轮 "排列,四个羧酸配体占据赤道位点,为双功能配体在轴向位点配位留出了空间。在七种结构中的五种结构中,NâHâ¯N 和 NâHâ¯O 氢键的组合推动了超分子化学反应,这种化学反应将配位复合物组织成所需的无限一维链。
  • Directed Supramolecular Assembly of Infinite 1-D M(II)-Containing Chains (M = Cu, Co, Ni) Using Structurally Bifunctional Ligands
    作者:Christer B. Aakeröy、Nate Schultheiss、John Desper
    DOI:10.1021/ic048405y
    日期:2005.7.1
    The directed assembly of six different M(II) complexes (M = Cu, Co, and Ni) into infinite chains has been achieved by combining anionic chelating ligands (for controlling the coordination geometry) with bifunctional ligands containing a metal-coordinating pyridyl moiety and a self-complementary hydrogen-bonding moiety. Six crystal structures are presented, and in each case, the chelating acac ligand occupies the four equatorial coordination sites leaving room for the bifunctional ligand to coordinate in the axial positions. The supramolecular chemistry, which organizes the coordination complexes into the desired infinite 1-D chains, is driven by a combination of N-H center dot center dot center dot N and N-H center dot center dot center dot O hydrogen bonds.
  • PYRIMIDINE DERIVATIVES AS HSP90 INHIBITORS
    申请人:Astex Therapeutics Limited
    公开号:EP2049497A2
    公开(公告)日:2009-04-22
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