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(R)-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]isoindol-5-one | 1131192-75-0

中文名称
——
中文别名
——
英文名称
(R)-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]isoindol-5-one
英文别名
——
(R)-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]isoindol-5-one化学式
CAS
1131192-75-0
化学式
C22H24N2O5
mdl
——
分子量
396.443
InChiKey
GMPCZFVIRMINOF-YCRPNKLZSA-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):
    2.99
  • 重原子数:
    29.0
  • 可旋转键数:
    5.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    60.47
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    (R)-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]isoindol-5-onemagnesium monoperoxyphthalate hexahydrate 作用下, 以 甲醇 为溶剂, 以84%的产率得到(R)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]-5H-isoindol-5-one
    参考文献:
    名称:
    A conceptually new approach to the asymmetric synthesis of 3-aryl and alkyl poly-substituted isoindolinones
    摘要:
    A conceptually new and efficient asymmetric synthesis of C-3 arylated or alkylated poly-substituted iso-indolinones is reported. The key step is the diastereoselective reduction of an N-acylhydrazonium species derived from the previously assembled corresponding hydroxyl derivative hearing the (S)-2-methoxymethylpyrrolidine (SMP) auxiliary. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2008.11.021
  • 作为产物:
    描述:
    7-hydroxy-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo-[4,5-f]-5H-isoindol-5-one三乙基硅烷三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 以81%的产率得到(R)-6-((S)-2-methoxymethylpyrrolidin-1-yl)-7-(4-methoxyphenyl)-6,7-dihydro-1,3-dioxolo[4,5-f]isoindol-5-one
    参考文献:
    名称:
    A conceptually new approach to the asymmetric synthesis of 3-aryl and alkyl poly-substituted isoindolinones
    摘要:
    A conceptually new and efficient asymmetric synthesis of C-3 arylated or alkylated poly-substituted iso-indolinones is reported. The key step is the diastereoselective reduction of an N-acylhydrazonium species derived from the previously assembled corresponding hydroxyl derivative hearing the (S)-2-methoxymethylpyrrolidine (SMP) auxiliary. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2008.11.021
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