摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-(3-allyl-1-{4-[3-allyl-4-(2-ethoxycarbonyl-ethyl)-2,5-dioxo-imidazolidin-1-yl]-butyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acid ethyl ester | 892495-98-6

中文名称
——
中文别名
——
英文名称
3-(3-allyl-1-{4-[3-allyl-4-(2-ethoxycarbonyl-ethyl)-2,5-dioxo-imidazolidin-1-yl]-butyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acid ethyl ester
英文别名
Ethyl 3-[1-[4-[4-(3-ethoxy-3-oxopropyl)-2,5-dioxo-3-prop-2-enylimidazolidin-1-yl]butyl]-2,5-dioxo-3-prop-2-enylimidazolidin-4-yl]propanoate
3-(3-allyl-1-{4-[3-allyl-4-(2-ethoxycarbonyl-ethyl)-2,5-dioxo-imidazolidin-1-yl]-butyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acid ethyl ester化学式
CAS
892495-98-6
化学式
C26H38N4O8
mdl
——
分子量
534.61
InChiKey
RVQWUJMMYQVAEP-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):
    1.6
  • 重原子数:
    38
  • 可旋转键数:
    19
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    134
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    3-(3-allyl-1-{4-[3-allyl-4-(2-ethoxycarbonyl-ethyl)-2,5-dioxo-imidazolidin-1-yl]-butyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acid ethyl esterRuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以46%的产率得到3-[16-(2-ethoxycarbonyl-ethyl)-8,15,17,18-tetraoxo-1,6,9,14-tetraaza-tricyclo[12.2.1.16,9]octadec-3-en-7-yl]-propionic acid ethyl ester
    参考文献:
    名称:
    Synthesis of N(3),N‘(3)-Polymethylene-bis-hydantoins and Their Macrocyclic Derivatives
    摘要:
    An efficient and straightforward two-step approach toward N(3), N'(3)-polymethylene-bis-hydantoins was developed. As a first step, a pyroglutamate is reacted with a diisocyanate to produce a bis-carbamoyllactam. The second step is a double-ring transformation by treatment of this bis-carbamoyllactam with KOtBu in ethanol. In this fashion N(3), N'(3)-polymethylene-bis-hydantoins are produced in two quantitative steps and under very mild conditions. When properly derivatized, these compounds can be converted to their macrocyclic derivatives upon treatment with 5 mol % of second-generation Grubbs' catalyst. These macrocyclic derivatives are so far not described in the literature. It was proven that exclusively (E)-isomers are formed.
    DOI:
    10.1021/jo060370r
  • 作为产物:
    描述:
    ethyl 1-({[4-({[2-(ethoxycarbonyl)-5-oxopyrrolidin-1-yl]carbonyl}amino)butyl]amino}carbonyl)-5-oxopyrrolidine-2-carboxylate 在 potassium tert-butylatepotassium carbonate 作用下, 以 乙醇丙酮 为溶剂, 反应 1.0h, 生成 3-(3-allyl-1-{4-[3-allyl-4-(2-ethoxycarbonyl-ethyl)-2,5-dioxo-imidazolidin-1-yl]-butyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acid ethyl ester
    参考文献:
    名称:
    Synthesis of N(3),N‘(3)-Polymethylene-bis-hydantoins and Their Macrocyclic Derivatives
    摘要:
    An efficient and straightforward two-step approach toward N(3), N'(3)-polymethylene-bis-hydantoins was developed. As a first step, a pyroglutamate is reacted with a diisocyanate to produce a bis-carbamoyllactam. The second step is a double-ring transformation by treatment of this bis-carbamoyllactam with KOtBu in ethanol. In this fashion N(3), N'(3)-polymethylene-bis-hydantoins are produced in two quantitative steps and under very mild conditions. When properly derivatized, these compounds can be converted to their macrocyclic derivatives upon treatment with 5 mol % of second-generation Grubbs' catalyst. These macrocyclic derivatives are so far not described in the literature. It was proven that exclusively (E)-isomers are formed.
    DOI:
    10.1021/jo060370r
点击查看最新优质反应信息