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7,8-didehydro-4,5-epoxy-17-methylmorphinan-2,6-diyl bis(naphthalene-1-carboxylate) | 633700-75-1

中文名称
——
中文别名
——
英文名称
7,8-didehydro-4,5-epoxy-17-methylmorphinan-2,6-diyl bis(naphthalene-1-carboxylate)
英文别名
morphine bis(1-naphthoate);Morphine di-(naphthalene-1-carboxylate);[(4R,4aR,7S,7aR,12bS)-3-methyl-9-(naphthalene-1-carbonyloxy)-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-yl] naphthalene-1-carboxylate
7,8-didehydro-4,5-epoxy-17-methylmorphinan-2,6-diyl bis(naphthalene-1-carboxylate)化学式
CAS
633700-75-1
化学式
C39H31NO5
mdl
——
分子量
593.679
InChiKey
OKMGZRBUYJWHFL-PLZSVQQGSA-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):
    7.3
  • 重原子数:
    45
  • 可旋转键数:
    6
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    65.1
  • 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

反应信息

  • 作为反应物:
    描述:
    magnesium monoperoxyphthalate hexahydrate 、 7,8-didehydro-4,5-epoxy-17-methylmorphinan-2,6-diyl bis(naphthalene-1-carboxylate)甲醇 为溶剂, 反应 0.75h, 生成
    参考文献:
    名称:
    使用非经典的Polonovski反应进一步研究叔胺生物碱的N-去甲基化作用。
    摘要:
    铁盐介导的Polonovski反应有效地将某些鸦片生物碱N-去甲基化。在该方法中,据报道使用叔N-甲基氧化胺的盐酸盐可以得到更好的所需N-脱甲基化产物的产率。在本文中,我们报告了在铁盐介导的Polonovski反应中使用N-氧化物盐的进一步研究。还描述了一种去除铁盐的有效方法,该方法极大地促进了N-nor产物的分离和纯化。
    DOI:
    10.1016/j.bmcl.2006.03.017
  • 作为产物:
    参考文献:
    名称:
    Inter- and intramolecular C—H...π interactions in morphine bis(1-naphthoate)
    摘要:
    The crystal structure of morphine bis(1-naphthoate) [ or 7,8-didehydro-4,5-epoxy-17-methylmorphinan- 2,6-diyl bis(naphthalene-1-carboxylate)], C39H31NO5, determined at 123 K, shows extensive C-H ...pi interactions in the crystal lattice. Of particular interest is an intramolecular C - H ...pi interaction within the unit cell between the two naphthoyl groups. Comparison of the opiate scaffolds of morphine bis( 1-naphthoate) and morphine shows only a small increase in strain due to the steric bulk of the naphthoyl groups. The crystal packing shows distinct areas of packing for the naphthalene/aromatic groups and the opiate backbone. Extensive inter- and intramolecular C - H...pi interactions lead to a densely packed aromatic region in the crystal lattice.
    DOI:
    10.1107/s0108270103015622
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文献信息

  • Inter- and intramolecular C—H...π interactions in morphine bis(1-naphthoate)
    作者:Nicholas Gathergood、Peter J. Scammells、Gary D. Fallon
    DOI:10.1107/s0108270103015622
    日期:2003.9.15
    The crystal structure of morphine bis(1-naphthoate) [ or 7,8-didehydro-4,5-epoxy-17-methylmorphinan- 2,6-diyl bis(naphthalene-1-carboxylate)], C39H31NO5, determined at 123 K, shows extensive C-H ...pi interactions in the crystal lattice. Of particular interest is an intramolecular C - H ...pi interaction within the unit cell between the two naphthoyl groups. Comparison of the opiate scaffolds of morphine bis( 1-naphthoate) and morphine shows only a small increase in strain due to the steric bulk of the naphthoyl groups. The crystal packing shows distinct areas of packing for the naphthalene/aromatic groups and the opiate backbone. Extensive inter- and intramolecular C - H...pi interactions lead to a densely packed aromatic region in the crystal lattice.
  • Further investigation of the N-demethylation of tertiary amine alkaloids using the non-classical Polonovski reaction
    作者:Shanti Thavaneswaran、Peter J. Scammells
    DOI:10.1016/j.bmcl.2006.03.017
    日期:2006.6
    iron salt-mediated Polonovski reaction efficiently N-demethylates certain opiate alkaloids. In this process, the use of the hydrochloride salt of the tertiary N-methyl amine oxide was reported to give better yields of the desired N-demethylated product. Herein, we report further investigation into the use of N-oxide salts in the iron salt-mediated Polonovski reaction. An efficient approach for the
    铁盐介导的Polonovski反应有效地将某些鸦片生物碱N-去甲基化。在该方法中,据报道使用叔N-甲基氧化胺的盐酸盐可以得到更好的所需N-脱甲基化产物的产率。在本文中,我们报告了在铁盐介导的Polonovski反应中使用N-氧化物盐的进一步研究。还描述了一种去除铁盐的有效方法,该方法极大地促进了N-nor产物的分离和纯化。
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