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

(S)-1-((2R,5S)-3,6-Diethoxy-5-isopropyl-2-methoxymethoxymethyl-2,5-dihydro-pyrazin-2-yl)-2-methyl-propan-1-ol | 219691-14-2

中文名称
——
中文别名
——
英文名称
(S)-1-((2R,5S)-3,6-Diethoxy-5-isopropyl-2-methoxymethoxymethyl-2,5-dihydro-pyrazin-2-yl)-2-methyl-propan-1-ol
英文别名
——
(S)-1-((2R,5S)-3,6-Diethoxy-5-isopropyl-2-methoxymethoxymethyl-2,5-dihydro-pyrazin-2-yl)-2-methyl-propan-1-ol化学式
CAS
219691-14-2
化学式
C18H34N2O5
mdl
——
分子量
358.478
InChiKey
ZXSZBBNATOLKIP-RLFYNMQTSA-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

物化性质

  • 沸点:
    430.902±35.00 °C(Press: 760.00 Torr)(predicted)
  • 密度:
    1.100±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.27
  • 重原子数:
    25.0
  • 可旋转键数:
    9.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    81.87
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    甲氧基-三氟甲基苯(S)-1-((2R,5S)-3,6-Diethoxy-5-isopropyl-2-methoxymethoxymethyl-2,5-dihydro-pyrazin-2-yl)-2-methyl-propan-1-ol4-二甲氨基吡啶三乙胺 作用下, 以 二氯甲烷 为溶剂, 生成 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (S)-1-((2R,5S)-3,6-diethoxy-5-isopropyl-2-methoxymethoxymethyl-2,5-dihydro-pyrazin-2-yl)-2-methyl-propyl ester
    参考文献:
    名称:
    Tin- or magnesium-mediated diastereoselective aldol-type reactions for the asymmetric synthesis of α-substituted serines
    摘要:
    Diastereoselective aldol-type reactions of ethyl (5S)-3,6-diethoxy-2,5-dihydro-5-isopropyl-2-pyrazine-carboxylate (5S)-3 with achiral aldehydes 8a-d was investigated by using Sn(OSO2CF3)(2)-N-ethylpiperizine and MgBr2-triethylamine. The reaction with Sn(II) between (5S)-3 and aliphatic aldehydes 8a,b proved to be quite different from that with Mg(II). On the other hand, Sn(II)- or Mg(II)-mediated aldol-type reactions of (5S)-3 with benzaldehyde Sc and 3-methyl-2-butenal 8d each afforded the same diastereomer as the major product. These aldol products were each converted to the corresponding alpha-substituted serines 6 and 7 as enantiomerically pure compounds. (C) 1998 Elsevier Science Ltd. AII rights reserved.
    DOI:
    10.1016/s0957-4166(98)00371-1
  • 作为产物:
    参考文献:
    名称:
    Tin- or magnesium-mediated diastereoselective aldol-type reactions for the asymmetric synthesis of α-substituted serines
    摘要:
    Diastereoselective aldol-type reactions of ethyl (5S)-3,6-diethoxy-2,5-dihydro-5-isopropyl-2-pyrazine-carboxylate (5S)-3 with achiral aldehydes 8a-d was investigated by using Sn(OSO2CF3)(2)-N-ethylpiperizine and MgBr2-triethylamine. The reaction with Sn(II) between (5S)-3 and aliphatic aldehydes 8a,b proved to be quite different from that with Mg(II). On the other hand, Sn(II)- or Mg(II)-mediated aldol-type reactions of (5S)-3 with benzaldehyde Sc and 3-methyl-2-butenal 8d each afforded the same diastereomer as the major product. These aldol products were each converted to the corresponding alpha-substituted serines 6 and 7 as enantiomerically pure compounds. (C) 1998 Elsevier Science Ltd. AII rights reserved.
    DOI:
    10.1016/s0957-4166(98)00371-1
点击查看最新优质反应信息