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1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethane | 166270-58-2

中文名称
——
中文别名
——
英文名称
1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethane
英文别名
1,2-bis(5-tert-butoxycarbonylpyrrole)ethane;tert-butyl 4-(3-methoxy-3-oxopropyl)-5-[2-[3-(3-methoxy-3-oxopropyl)-4-methyl-5-[(2-methylpropan-2-yl)oxycarbonyl]-1H-pyrrol-2-yl]ethyl]-3-methyl-1H-pyrrole-2-carboxylate
1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethane化学式
CAS
166270-58-2
化学式
C30H44N2O8
mdl
——
分子量
560.688
InChiKey
ANOCQBLSQQAQLF-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):
    5
  • 重原子数:
    40
  • 可旋转键数:
    17
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    137
  • 氢给体数:
    2
  • 氢受体数:
    8

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:
    1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethane硫酸三氟乙酸 作用下, 反应 6.5h, 生成 2,3,6,7,11,18-Hexamethyl-12,17-bis-(2-methoxycarbonylethyl)-corrphycene
    参考文献:
    名称:
    On the chemistry of pyrrole pigments, XCVI: An efficient synthesis of corrphycenes
    摘要:
    By means of copper catalyzed intramolecular coupling of the easily accessible 1,2-bis-(1-iodo-dipyrrin-9-yl)-ethanes and subsequent demetallation of the intermediate copper complexes corrphycenes could be prepared in nearly 40% overall yields.
    DOI:
    10.1007/bf00807410
  • 作为产物:
    描述:
    1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethene 在 palladium on activated charcoal 甲醇magnesium 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以95%的产率得到1,2-bis(5-tert-butoxycarbonyl-4-methyl-3-methoxycarbonylethylpyrrolyl)-ethane
    参考文献:
    名称:
    On the chemistry of pyrrole pigments, XCII: Syntheses of 1,2-bis-pyrrolylethanes
    摘要:
    1,2-bis-Pyrrolylethanes are potential synthesis precursors of b-homorubins. They were synthesized in two ways: by self coupling of a 5-halomethylpyrrole using VCl3/LiAlH4 or by the reduction of 1,2-bis-pyrrolylethenes using Mg-MeOH/Pd-C as catalyst. The yields were 30-40% for the first method and reached 80% for the second one.
    DOI:
    10.1007/bf00813210
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文献信息

  • An Efficient Preparation of 1,2-Bis(Dipyrrin-9-Ylene)-Ethane, the First Fully Conjugated<i>b</i>-Homobilin
    作者:Qingqi Chen、Bingzi Chen、Xiaoli Li
    DOI:10.1080/00397910008087334
    日期:2000.2
    Abstract 1,2-Bis(dipyrrin-9-ylene)-ethane 1, the first fully conjugated b-homobilin, was synthesized in two steps with excellent yield by first condensing 1,2-bispyrrylethane 3 with 2 molecular 5-formylpyrrole 4, followed by dehydration of the result 1,2-Bis(dipyrrin-9-yl)-ethane 2 with DDQ in dichloromethane. The chemical and spectroscopic properties of this novel chromophoric system are discussed
    摘要 1,2-双(二吡喃-9-亚苯基)-乙烷1,第一个完全共轭的b-homobilin,通过首先将1,2-双吡咯烷3与2分子的5-甲酰基吡咯4缩合,分两步合成,收率优异然后在二氯甲烷中用 DDQ 使所得的 1,2-双(二吡喃-9-基)-乙烷 2 脱水。讨论了这种新型发色系统的化学和光谱特性。
  • An Efficient Route to 1,2-BIS(9′-Bromodipyrrin)ethane
    作者:Q. Chen、X. Li、B. Chen
    DOI:10.1080/00397919808004443
    日期:1998.9
    1,2-Bis(9-bromodipyrrin)-ethane, an important imtermediate for isoporphyrins (porphyrin isomers), homo-biliverdins and -bilrubins, is synthesized with excellent yield by bromination of the corresponding 1,2-bis(9-carboxydipyrrin)-ethane, which is distinctly shorter and more efficient than the literature report.
  • On the chemistry of pyrrole pigments, XCVI: An efficient synthesis of corrphycenes
    作者:H. Falk、Q. -Q. Chen
    DOI:10.1007/bf00807410
    日期:1996.1
    By means of copper catalyzed intramolecular coupling of the easily accessible 1,2-bis-(1-iodo-dipyrrin-9-yl)-ethanes and subsequent demetallation of the intermediate copper complexes corrphycenes could be prepared in nearly 40% overall yields.
  • On the chemistry of pyrrole pigments, XCII: Syntheses of 1,2-bis-pyrrolylethanes
    作者:Q. -Q. Chen、H. Falk、R. Micura
    DOI:10.1007/bf00813210
    日期:1995.4
    1,2-bis-Pyrrolylethanes are potential synthesis precursors of b-homorubins. They were synthesized in two ways: by self coupling of a 5-halomethylpyrrole using VCl3/LiAlH4 or by the reduction of 1,2-bis-pyrrolylethenes using Mg-MeOH/Pd-C as catalyst. The yields were 30-40% for the first method and reached 80% for the second one.
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