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(1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-4-(4-(4-(tert-butoxycarbonyl)piperazine-1-carbonyl)piperazin-1-yl)-6-hydroxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate | 1042129-75-8

中文名称
——
中文别名
——
英文名称
(1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-4-(4-(4-(tert-butoxycarbonyl)piperazine-1-carbonyl)piperazin-1-yl)-6-hydroxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate
英文别名
——
(1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-4-(4-(4-(tert-butoxycarbonyl)piperazine-1-carbonyl)piperazin-1-yl)-6-hydroxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate 化学式
CAS
1042129-75-8
化学式
C32H51N5O14
mdl
——
分子量
729.782
InChiKey
IKISABDMAWNVBP-UTRGJRIPSA-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):
    -0.77
  • 重原子数:
    51.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    220.09
  • 氢给体数:
    2.0
  • 氢受体数:
    15.0

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:
    (1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-4-(4-(4-(tert-butoxycarbonyl)piperazine-1-carbonyl)piperazin-1-yl)-6-hydroxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate 三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以95%的产率得到(1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-6-hydroxy-6-(methoxycarbonyl)-4-(4-(piperazine-1-carbonyl)piperazin-1-yl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate
    参考文献:
    名称:
    Simultaneous 2-O-deacetylation and 4-amination of peracetylated Neu5Ac: application to the synthesis of (4→4)-piperazine derivatives linked sialic acid dimers
    摘要:
    A simultaneous stereoselective 2-O-deacetylation and 4-amination reaction of peracetylated Neu5Ac 1 has been established with cyclic secondary amines, such as 1-N-Boc-piperazine. Four C-2-symmetric and two asymmetric sialic acid dimers with (4 -> 4)-piperazine derivatives linked were synthesized. They may serve as precursors of unnatural polysialic acids. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.04.046
  • 作为产物:
    描述:
    methyl (2S,4S,5R,6R)-5-acetamido-2-hydroxy-4-piperazin-1-yl-6-[(1S,2R)-1,2,3-triacetyloxypropyl]oxane-2-carboxylate三光气N-Boc-哌嗪三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.5h, 以202 mg的产率得到(1S,2R)-1-((2R,3R,4S,6S)-3-acetamido-4-(4-(4-(tert-butoxycarbonyl)piperazine-1-carbonyl)piperazin-1-yl)-6-hydroxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate
    参考文献:
    名称:
    Simultaneous 2-O-deacetylation and 4-amination of peracetylated Neu5Ac: application to the synthesis of (4→4)-piperazine derivatives linked sialic acid dimers
    摘要:
    A simultaneous stereoselective 2-O-deacetylation and 4-amination reaction of peracetylated Neu5Ac 1 has been established with cyclic secondary amines, such as 1-N-Boc-piperazine. Four C-2-symmetric and two asymmetric sialic acid dimers with (4 -> 4)-piperazine derivatives linked were synthesized. They may serve as precursors of unnatural polysialic acids. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.04.046
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