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ethyl 3-oxo-3-ethyl-N-methyl>aminopropionate | 154308-10-8

中文名称
——
中文别名
——
英文名称
ethyl 3-oxo-3-ethyl-N-methyl>aminopropionate
英文别名
Ethyl 3-[(3-ethoxy-3-oxopropanoyl)-methylamino]-3-pyridin-2-ylpropanoate
ethyl 3-oxo-3-<N-<2-ethoxycarbonyl-1-(2-pyridinyl)>ethyl-N-methyl>aminopropionate化学式
CAS
154308-10-8
化学式
C16H22N2O5
mdl
——
分子量
322.361
InChiKey
NNMOAROHONYFIF-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):
    0.8
  • 重原子数:
    23
  • 可旋转键数:
    10
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    85.8
  • 氢给体数:
    0
  • 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:
    参考文献:
    名称:
    Synthesis ofC-nor-4,6-secocamptothecin and related compounds
    摘要:
    AbstractC‐nor‐4,6‐Secocamptothecin 2, 4‐ethyl‐4‐hydroxy‐6‐(2‐quinolinyl)‐1H‐pyrano[3,4‐c]pyridine‐3,8(4H,7H)‐dione, lacking the C‐ring of camptothecin 1, and its related compounds 3 and 4 were prepared from ethyl quinoline‐2‐carboxylate 7. By an analogous reaction sequences, synthesis of 6‐(2‐pyridinyl)‐1H‐pyrano[3,4‐c]‐pyridine‐3,8(4H7H)‐dione derivatives 5 and 6, which contain the B, D, and E ring of 1, were achieved.
    DOI:
    10.1002/jhet.5570300311
  • 作为产物:
    描述:
    皮考林乙酸乙酯 在 palladium on activated charcoal sodium tetrahydroborate 、 甲酸氢气N,N'-二环己基碳二亚胺 作用下, 以 甲醇二氯甲烷 为溶剂, 25.0 ℃ 、98.06 kPa 条件下, 反应 18.5h, 生成 ethyl 3-oxo-3-ethyl-N-methyl>aminopropionate
    参考文献:
    名称:
    Synthesis ofC-nor-4,6-secocamptothecin and related compounds
    摘要:
    AbstractC‐nor‐4,6‐Secocamptothecin 2, 4‐ethyl‐4‐hydroxy‐6‐(2‐quinolinyl)‐1H‐pyrano[3,4‐c]pyridine‐3,8(4H,7H)‐dione, lacking the C‐ring of camptothecin 1, and its related compounds 3 and 4 were prepared from ethyl quinoline‐2‐carboxylate 7. By an analogous reaction sequences, synthesis of 6‐(2‐pyridinyl)‐1H‐pyrano[3,4‐c]‐pyridine‐3,8(4H7H)‐dione derivatives 5 and 6, which contain the B, D, and E ring of 1, were achieved.
    DOI:
    10.1002/jhet.5570300311
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文献信息

  • Synthesis of<i>C</i>-nor-4,6-secocamptothecin and related compounds
    作者:Takushi Kurihara、Hirokatsu Tanno、Shigetaka Takemura、Shinya Harusawa、Ryuji Yoneda
    DOI:10.1002/jhet.5570300311
    日期:1993.5
    AbstractC‐nor‐4,6‐Secocamptothecin 2, 4‐ethyl‐4‐hydroxy‐6‐(2‐quinolinyl)‐1H‐pyrano[3,4‐c]pyridine‐3,8(4H,7H)‐dione, lacking the C‐ring of camptothecin 1, and its related compounds 3 and 4 were prepared from ethyl quinoline‐2‐carboxylate 7. By an analogous reaction sequences, synthesis of 6‐(2‐pyridinyl)‐1H‐pyrano[3,4‐c]‐pyridine‐3,8(4H7H)‐dione derivatives 5 and 6, which contain the B, D, and E ring of 1, were achieved.
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