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2-chloro-N6-methyladenosine-5'-N-methyl uronamide | 1012864-79-7

中文名称
——
中文别名
——
英文名称
2-chloro-N6-methyladenosine-5'-N-methyl uronamide
英文别名
(2S,3S,4R,5R)-5-[2-chloro-6-(methylamino)purin-9-yl]-3,4-dihydroxy-N-methyloxolane-2-carboxamide
2-chloro-N<sup>6</sup>-methyladenosine-5'-N-methyl uronamide化学式
CAS
1012864-79-7
化学式
C12H15ClN6O4
mdl
——
分子量
342.742
InChiKey
ZRXNIMHNBFDMAC-QMWPFBOUSA-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):
    -0.3
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    134
  • 氢给体数:
    4
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    methyl 1-[2,6-dichloropurin-9-yl]-2,3-di-O-acetyl-β-D-ribofuronate 、 甲胺四氢呋喃 为溶剂, 反应 0.33h, 以65%的产率得到2-chloro-N6-methyladenosine-5'-N-methyl uronamide
    参考文献:
    名称:
    An efficient convergent synthesis of adenosine-5′-N-alkyluronamides
    摘要:
    Herein we report an efficient synthesis of adenosine-5'-N-alkyluronamides in which an enzyme-mediated deacetylation reaction is a key to the selective modification of the 5'-N-position, prior to coupling the ribose and purine components via a microwave-assisted Vorbruggen coupling. This approach provides access to highly functionalised adenosines with 2- and N-6-substitutents, which can be incorporated before or after the ribose-coupling step. In all cases the microwave-assisted Vorbruggen coupling conditions afforded anomerically pure purine ribosides in good to excellent yields. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.11.100
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文献信息

  • An efficient convergent synthesis of adenosine-5′-N-alkyluronamides
    作者:Shane M. Devine、Peter J. Scammells
    DOI:10.1016/j.tet.2007.11.100
    日期:2008.2
    Herein we report an efficient synthesis of adenosine-5'-N-alkyluronamides in which an enzyme-mediated deacetylation reaction is a key to the selective modification of the 5'-N-position, prior to coupling the ribose and purine components via a microwave-assisted Vorbruggen coupling. This approach provides access to highly functionalised adenosines with 2- and N-6-substitutents, which can be incorporated before or after the ribose-coupling step. In all cases the microwave-assisted Vorbruggen coupling conditions afforded anomerically pure purine ribosides in good to excellent yields. (C) 2007 Elsevier Ltd. All rights reserved.
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