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N-benzyl-2-amino-4,6-dimethoxypyrimidine

中文名称
——
中文别名
——
英文名称
N-benzyl-2-amino-4,6-dimethoxypyrimidine
英文别名
N-benzyl-4,6-dimethoxypyrimidin-2-amine
N-benzyl-2-amino-4,6-dimethoxypyrimidine化学式
CAS
——
化学式
C13H15N3O2
mdl
——
分子量
245.281
InChiKey
IIYOIWWQKJCGBL-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):
    2.6
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    56.3
  • 氢给体数:
    1
  • 氢受体数:
    5

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:
    N-benzyl-2-amino-4,6-dimethoxypyrimidine盐酸 作用下, 以 为溶剂, 反应 12.0h, 以90%的产率得到1-苄基胍盐酸盐
    参考文献:
    名称:
    Using N-substituted-2-amino-4,6-dimethoxypyrimidines in the synthesis of aliphatic guanidines
    摘要:
    The use of 2-chloro-4,6-dimethoxypyrimdine as a tool for the syntheses of substituted guanidines is presented. This method, that we had previously shown to be very useful for aromatic amines, introduces an atom economical, cost effective and environmentally functionality in aliphatic primary and secondary amin safe method for the installation of the guanidine (C) 2015 Elsevier Ltd. All rights reserved.d
    DOI:
    10.1016/j.tetlet.2015.07.007
  • 作为产物:
    描述:
    苄胺2-氯-4,6-二甲氧基嘧啶N,N-二异丙基乙胺 作用下, 以 异丙醇 为溶剂, 反应 0.67h, 以93%的产率得到N-benzyl-2-amino-4,6-dimethoxypyrimidine
    参考文献:
    名称:
    微波辅助合成氨基嘧啶
    摘要:
    通过微波辅助的芳族亲核取代或Suzuki偶联合成了一系列的单或双取代的氨基嘧啶衍生物。
    DOI:
    10.1016/s0040-4039(02)01190-5
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文献信息

  • NEUROPROTECTIVE MULTIFUNCTIONAL ANTIOXIDANTS AND THEIR MONOFUNCTIONAL ANALOGS
    申请人:KADOR PETER F.
    公开号:US20140235858A1
    公开(公告)日:2014-08-21
    The neuroprotective multifunctional antioxidants are compounds that contain a 2-diacetylamino-5-hydroxypyrimidine moiety, having the structural formula: wherein R 1 is CH 2 or C 2 H 4 ; R 2 is H or —OR 4 where R 4 is H or aryl; and R 3a and R 3b are independently selected from the group consisting of H and —O-alkyl. The antioxidants are orally bioavailable metal-attenuating multifunctional antioxidants that can independently attenuate transition metals, as well as scavenger free radicals. The multifunctional antioxidant compounds, by their ability to independently chelate metals, such as Fe, Cu or Zn, and scavenge free radicals generated from different sources, are neuroprotective and are beneficial for the treatment of various neurological disorders, such as Alzheimer's disease, Parkinson's disease, ALS, traumatic brain injury, ocular disorders, such as cataract, glaucoma, age-related macular degeneration and other retinal degeneration, as well as for reducing the progression of diabetic complications.
    神经保护多功能抗氧化剂是含有2-二乙酰氨基-5-羟基嘧啶基团的化合物,具有以下结构式: 其中R1为CH2或C2H4;R2为H或—OR4,其中R4为H或芳基;R3a和R3b分别独立地选自H和—O-烷基的组。这些抗氧化剂是口服可利用的金属减弱多功能抗氧化剂,可以独立减弱过渡金属,以及清除自由基。由于这些多功能抗氧化剂化合物具有独立螯合金属(如Fe、Cu或Zn)和清除来自不同来源产生的自由基的能力,它们具有神经保护作用,并有助于治疗各种神经系统疾病,如阿尔茨海默病、帕金森病、肌萎缩侧索硬化症、创伤性脑损伤、眼部疾病(如白内障、青光眼、老年性黄斑变性和其他视网膜变性),以及减缓糖尿病并发症的进展。
  • Microwave-assisted synthesis of aminopyrimidines
    作者:Guanglin Luo、Ling Chen、Graham S Poindexter
    DOI:10.1016/s0040-4039(02)01190-5
    日期:2002.8
    Series of mono- or di-substituted aminopyrimidine derivatives were synthesized through microwave-assisted aromatic nucleophilic substitution or Suzuki coupling.
    通过微波辅助的芳族亲核取代或Suzuki偶联合成了一系列的单或双取代的氨基嘧啶衍生物。
  • Orally Bioavailable Metal Chelators and Radical Scavengers: Multifunctional Antioxidants for the Coadjutant Treatment of Neurodegenerative Diseases
    作者:Hiroyoshi Kawada、Peter F. Kador
    DOI:10.1021/acs.jmedchem.5b00272
    日期:2015.11.25
    Neurodegenerative diseases are associated with oxidative stress that is induced by the presence of reactive oxygen species and the abnormal cellular accumulation of transition metals. Here, a new series of orally bioavailable multifunctional antioxidants (MFAO-2s) possessing a 2-diacetylamino-5-hydroxypyrimidine moiety is described. These MFAO-2s demonstrate both free radical and metal attenuating properties that are similar to the original published MFAO-1s that are based on 1-N,N'-dimethylsulfamoyl-1-4-(2-pyrimidyl)piperazine. Oral bioavailability studies in C57BL/6 mice demonstrate that the MFAO-2s accumulate in the brain at significantly higher levels than the MFAO-1s while achieving similar neural retina levels. The MFAO-2s protect human neuroblastoma and retinal pigmented epithelial cells against hydroxyl radicals in a dose-dependent manner by maintaining cell viability and intracellular glutathione levels. The MFAO-2s outperform clioquinol, a metal attenuator that has been investigated for the treatment of Alzheimer's disease.
  • EP2956140A1
    申请人:——
    公开号:EP2956140A1
    公开(公告)日:2015-12-23
  • US8877766B2
    申请人:——
    公开号:US8877766B2
    公开(公告)日:2014-11-04
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