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

diethyl 2-(1-benzyloxy-5-(4-nitrophenyl)-pyrazol-4-yl)-2-tert-butoxycarbonylamino-malonate | 439100-82-0

中文名称
——
中文别名
——
英文名称
diethyl 2-(1-benzyloxy-5-(4-nitrophenyl)-pyrazol-4-yl)-2-tert-butoxycarbonylamino-malonate
英文别名
diethyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-[5-(4-nitrophenyl)-1-phenylmethoxypyrazol-4-yl]propanedioate
diethyl 2-(1-benzyloxy-5-(4-nitrophenyl)-pyrazol-4-yl)-2-tert-butoxycarbonylamino-malonate化学式
CAS
439100-82-0
化学式
C28H32N4O9
mdl
——
分子量
568.583
InChiKey
DEMBGKDQMZDMLD-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):
    3.93
  • 重原子数:
    41.0
  • 可旋转键数:
    11.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    161.12
  • 氢给体数:
    1.0
  • 氢受体数:
    11.0

反应信息

  • 作为反应物:
    描述:
    diethyl 2-(1-benzyloxy-5-(4-nitrophenyl)-pyrazol-4-yl)-2-tert-butoxycarbonylamino-malonate盐酸 作用下, 反应 12.0h, 以94%的产率得到hydrochloride salt of amino-[1-hydroxy-5-(4-nitrophenyl)-pyrazol-4-yl]-acetic acid
    参考文献:
    名称:
    Synthesis of 1-hydroxypyrazole glycine derivatives
    摘要:
    A series of novel alpha-amino acids containing the 1-hydroxypyrazole ring has been prepared by addition of organomagnesium or organolithium intermediates to diethyl N-Boc-iminomalonate as an electrophilic glycine equivalent. Electrophiles, aryl and heteroaryl substituents were introduced in the pyrazole ring. (C) 2002 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(02)00021-2
  • 作为产物:
    参考文献:
    名称:
    Synthesis of 1-hydroxypyrazole glycine derivatives
    摘要:
    A series of novel alpha-amino acids containing the 1-hydroxypyrazole ring has been prepared by addition of organomagnesium or organolithium intermediates to diethyl N-Boc-iminomalonate as an electrophilic glycine equivalent. Electrophiles, aryl and heteroaryl substituents were introduced in the pyrazole ring. (C) 2002 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(02)00021-2
点击查看最新优质反应信息