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tert-butyl 2-(3-(1-benzylpiperidin-4-yl)ureido)ethylcarbamate | 1323277-04-8

中文名称
——
中文别名
——
英文名称
tert-butyl 2-(3-(1-benzylpiperidin-4-yl)ureido)ethylcarbamate
英文别名
tert-butyl N-[2-[(1-benzylpiperidin-4-yl)carbamoylamino]ethyl]carbamate
tert-butyl 2-(3-(1-benzylpiperidin-4-yl)ureido)ethylcarbamate化学式
CAS
1323277-04-8
化学式
C20H32N4O3
mdl
——
分子量
376.499
InChiKey
NCMCZTJPTJRPDO-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):
    2.2
  • 重原子数:
    27
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    82.7
  • 氢给体数:
    3
  • 氢受体数:
    4

上下游信息

  • 上游原料
    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:
    tert-butyl 2-(3-(1-benzylpiperidin-4-yl)ureido)ethylcarbamate 在 palladium on activated charcoal 、 氢气potassium carbonate三氟乙酸 作用下, 以 乙醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 20.0~80.0 ℃ 、101.33 kPa 条件下, 反应 2.0h, 生成 1-(2-aminoethyl)-3-(1-(2-fluoroethyl)piperidin-4-yl)urea
    参考文献:
    名称:
    Synthesis and Cardiac Imaging of 18F-Ligands Selective for β1-Adrenoreceptors
    摘要:
    A series of potent and selective beta(1)-adrenoreceptor ligands were identified (IC50 range, 0.04-0.25 nM; beta(1)/beta(2) selectivity range, 65-450-fold), labeled with the PET radioisotope fluorine-18 and evaluated in normal Sprague-Dawley rats. Tissue distribution studies demonstrated uptake of each radiotracers from the blood pool into the myocardium (0.48-0.62% ID/g), lung (0.63-0.97% ID/g), and liver (1.03-1.14% ID/g). Dynamic mu PET imaging confirmed the in vivo dissection studies.
    DOI:
    10.1021/ml1002458
  • 作为产物:
    参考文献:
    名称:
    Synthesis and Cardiac Imaging of 18F-Ligands Selective for β1-Adrenoreceptors
    摘要:
    A series of potent and selective beta(1)-adrenoreceptor ligands were identified (IC50 range, 0.04-0.25 nM; beta(1)/beta(2) selectivity range, 65-450-fold), labeled with the PET radioisotope fluorine-18 and evaluated in normal Sprague-Dawley rats. Tissue distribution studies demonstrated uptake of each radiotracers from the blood pool into the myocardium (0.48-0.62% ID/g), lung (0.63-0.97% ID/g), and liver (1.03-1.14% ID/g). Dynamic mu PET imaging confirmed the in vivo dissection studies.
    DOI:
    10.1021/ml1002458
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文献信息

  • Synthesis and Cardiac Imaging of <sup>18</sup>F-Ligands Selective for β<sub>1</sub>-Adrenoreceptors
    作者:Heike S. Radeke、Ajay Purohit、Thomas D. Harris、Kelley Hanson、Reinaldo Jones、Carol Hu、Padmaja Yalamanchili、Megan Hayes、Ming Yu、Mary Guaraldi、Mikhail Kagan、Michael Azure、Michael Cdebaca、Simon Robinson、David Casebier
    DOI:10.1021/ml1002458
    日期:2011.9.8
    A series of potent and selective beta(1)-adrenoreceptor ligands were identified (IC50 range, 0.04-0.25 nM; beta(1)/beta(2) selectivity range, 65-450-fold), labeled with the PET radioisotope fluorine-18 and evaluated in normal Sprague-Dawley rats. Tissue distribution studies demonstrated uptake of each radiotracers from the blood pool into the myocardium (0.48-0.62% ID/g), lung (0.63-0.97% ID/g), and liver (1.03-1.14% ID/g). Dynamic mu PET imaging confirmed the in vivo dissection studies.
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