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2-benzamido-7-<2-(benzoyloxy)ethyl>purin-6-one | 124471-17-6

中文名称
——
中文别名
——
英文名称
2-benzamido-7-<2-(benzoyloxy)ethyl>purin-6-one
英文别名
2-(2-(Benzoylamino)-6-hydroxy-7H-purin-7-yl)ethyl benzoate;2-(2-benzamido-6-oxo-1H-purin-7-yl)ethyl benzoate
2-benzamido-7-<2-(benzoyloxy)ethyl>purin-6-one化学式
CAS
124471-17-6
化学式
C21H17N5O4
mdl
——
分子量
403.397
InChiKey
USPKQGSSAICBHS-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:
    30
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    115
  • 氢给体数:
    2
  • 氢受体数:
    6

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
  • 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:
    2-benzamido-7-<2-(benzoyloxy)ethyl>purin-6-one盐酸sodium methylate 作用下, 以 甲醇 为溶剂, 以79%的产率得到2-benzamido-7-(2-hydroxyethyl)purin-6-one
    参考文献:
    名称:
    Synthesis and binding properties of monomeric and dimeric guanine and cytosine amine derivatives
    摘要:
    The syntheses of the N-protected forms of the cytosine homodimer 1, the guanine cytosine heterodimer 2, and the guanine homodimer 3 are described. Derivatization of these dimers, as well as the protected monomers corresponding to 4 and 5, with omega-methoxypoly(ethylene glycol)-alpha-carboxylic acid 26 and subsequent deprotection formed the amides 29, 31, 33, 35, and 37. The binding properties of these solubilized compounds in DMSO-d(g) were examined using H-1 NMR.
    DOI:
    10.1021/jo00029a008
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and binding properties of monomeric and dimeric guanine and cytosine amine derivatives
    摘要:
    The syntheses of the N-protected forms of the cytosine homodimer 1, the guanine cytosine heterodimer 2, and the guanine homodimer 3 are described. Derivatization of these dimers, as well as the protected monomers corresponding to 4 and 5, with omega-methoxypoly(ethylene glycol)-alpha-carboxylic acid 26 and subsequent deprotection formed the amides 29, 31, 33, 35, and 37. The binding properties of these solubilized compounds in DMSO-d(g) were examined using H-1 NMR.
    DOI:
    10.1021/jo00029a008
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文献信息

  • SESSLER, JONATHAN L.;MAGDA, DARREN J.;LYNCH, VINCENT;SCHIFF, GILBERT M.;B+, NUCLEOSIDES AND NUCLEOTIDES, 8,(1989) N, C. 431-448
    作者:SESSLER, JONATHAN L.、MAGDA, DARREN J.、LYNCH, VINCENT、SCHIFF, GILBERT M.、B+
    DOI:——
    日期:——
  • SESSLER, JONATHAN L.;MAGDA, DARREN;HUGDAHL, JEFF, J. NUCL. PHENOM., 7,(1989) N, C. 19-26
    作者:SESSLER, JONATHAN L.、MAGDA, DARREN、HUGDAHL, JEFF
    DOI:——
    日期:——
  • Synthesis and binding properties of monomeric and dimeric guanine and cytosine amine derivatives
    作者:Jonathan L. Sessler、Darren Magda、Hiroyuki Furuta
    DOI:10.1021/jo00029a008
    日期:1992.1
    The syntheses of the N-protected forms of the cytosine homodimer 1, the guanine cytosine heterodimer 2, and the guanine homodimer 3 are described. Derivatization of these dimers, as well as the protected monomers corresponding to 4 and 5, with omega-methoxypoly(ethylene glycol)-alpha-carboxylic acid 26 and subsequent deprotection formed the amides 29, 31, 33, 35, and 37. The binding properties of these solubilized compounds in DMSO-d(g) were examined using H-1 NMR.
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