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(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-methoxy-4-((2-(tosylimino)-2H-chromen-3-yl)methoxy)tetrahydro-2H-pyran-3,5-diyl diacetate | 1619921-28-6

中文名称
——
中文别名
——
英文名称
(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-methoxy-4-((2-(tosylimino)-2H-chromen-3-yl)methoxy)tetrahydro-2H-pyran-3,5-diyl diacetate
英文别名
——
(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-methoxy-4-((2-(tosylimino)-2H-chromen-3-yl)methoxy)tetrahydro-2H-pyran-3,5-diyl diacetate化学式
CAS
1619921-28-6
化学式
C30H33NO12S
mdl
——
分子量
631.658
InChiKey
NMUNEDUPVDAOQR-AHHNXVMKSA-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

物化性质

  • 沸点:
    711.1±70.0 °C(predicted)
  • 密度:
    1.37±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.71
  • 重原子数:
    44.0
  • 可旋转键数:
    10.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    166.23
  • 氢给体数:
    0.0
  • 氢受体数:
    12.0

反应信息

  • 作为反应物:
    描述:
    (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-methoxy-4-((2-(tosylimino)-2H-chromen-3-yl)methoxy)tetrahydro-2H-pyran-3,5-diyl diacetatesodium methylate 作用下, 以 甲醇 为溶剂, 反应 1.0h, 以61%的产率得到N-[3-[[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-methoxyoxan-4-yl]oxymethyl]chromen-2-ylidene]-4-methylbenzenesulfonamide
    参考文献:
    名称:
    Synthesis and evaluation of iminocoumaryl and coumaryl derivatized glycosides as galectin antagonists
    摘要:
    A collection of iminocoumarylmethyl glycoside derivatives have been prepared by copper-catalyzed multi-component reaction of carbohydrate propargyl derivatives, sulfonyl azides, and salicylaldehyde or o-hydroxy acetophenone. The method is simple, versatile to all three components, and exceptionally high yielding. The carbohydrate N-sulfonyl iminocoumarine hybrid molecules were evaluated for binding galectin-1, -2, -3, -4 N, -4C, -7, -8 N, -9 N, and 9C using a competitive fluorescence polarization assay. Selective compounds were identified against galectin-3, 7, 8 N, and 9 N with up to 40-fold affinity enhancements relative to methyl alpha-D-galactopyranoside due to the coumarylmethyl moieties. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.05.063
  • 作为产物:
    描述:
    methyl 2,4,6-tri-O-acetyl-3-prop-2-ynyl-α-D-galactopyranoside对甲苯磺酸钠水杨醛copper(l) iodide三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 13.0h, 以83%的产率得到(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-methoxy-4-((2-(tosylimino)-2H-chromen-3-yl)methoxy)tetrahydro-2H-pyran-3,5-diyl diacetate
    参考文献:
    名称:
    Synthesis and evaluation of iminocoumaryl and coumaryl derivatized glycosides as galectin antagonists
    摘要:
    A collection of iminocoumarylmethyl glycoside derivatives have been prepared by copper-catalyzed multi-component reaction of carbohydrate propargyl derivatives, sulfonyl azides, and salicylaldehyde or o-hydroxy acetophenone. The method is simple, versatile to all three components, and exceptionally high yielding. The carbohydrate N-sulfonyl iminocoumarine hybrid molecules were evaluated for binding galectin-1, -2, -3, -4 N, -4C, -7, -8 N, -9 N, and 9C using a competitive fluorescence polarization assay. Selective compounds were identified against galectin-3, 7, 8 N, and 9 N with up to 40-fold affinity enhancements relative to methyl alpha-D-galactopyranoside due to the coumarylmethyl moieties. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.05.063
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