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(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-3,4-dihydroxypiperidine | 1254754-97-6

中文名称
——
中文别名
——
英文名称
(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-3,4-dihydroxypiperidine
英文别名
——
(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-3,4-dihydroxypiperidine化学式
CAS
1254754-97-6
化学式
C28H31N3O8
mdl
——
分子量
537.569
InChiKey
BFBLHNFDWSYRSL-FOJDRRPASA-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):
    1.7
  • 重原子数:
    39.0
  • 可旋转键数:
    6.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    145.71
  • 氢给体数:
    3.0
  • 氢受体数:
    8.0

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

反应信息

  • 作为反应物:
    描述:
    (3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-3,4-dihydroxypiperidine甲基磺酰氯吡啶 作用下, 反应 2.0h, 以380 mg的产率得到(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-3-hydroxy-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-4-methanesulfonyloxypiperidine
    参考文献:
    名称:
    Synthesis and DNA cleavage evaluation of epoxypiperidine derivatives bearing a dehydroamino acid unit
    摘要:
    Epoxypiperidine derivatives bearing a dehydroamino acid unit were designed and synthesized as novel DNA alkylating agents based on the structure of azinomycins. A relaxation assay of plasmid DNA revealed that the epoxypiperidine derivative 3 has a DNA cleavage activity. Based on the studies, it would appear that the electron density of the amino group of epoxypiperidines plays a critically important role in the DNA cleavage. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.08.027
  • 作为产物:
    描述:
    四氢吡咯4-[(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-3,4-dihydroxypiperidin-2-ylidene]-2-(1-naphthyl)-4H-oxazol-5-one四氢呋喃 为溶剂, 反应 0.25h, 以450 mg的产率得到(3R,4S,5R)-5-acetoxy-N-allyloxycarbonyl-2-[(E)-1-(1-pyrrolidinyl)carbonyl-1-(1-naphthoyl)amino]methylidene-3,4-dihydroxypiperidine
    参考文献:
    名称:
    Synthesis and DNA cleavage evaluation of epoxypiperidine derivatives bearing a dehydroamino acid unit
    摘要:
    Epoxypiperidine derivatives bearing a dehydroamino acid unit were designed and synthesized as novel DNA alkylating agents based on the structure of azinomycins. A relaxation assay of plasmid DNA revealed that the epoxypiperidine derivative 3 has a DNA cleavage activity. Based on the studies, it would appear that the electron density of the amino group of epoxypiperidines plays a critically important role in the DNA cleavage. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.08.027
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