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tert-butyl N-[4-butoxy-3-[[5-[(2-butoxy-5-formylbenzoyl)amino]-2,4-bis(2-methylpropoxy)phenyl]carbamoyl]phenyl]carbamate | 1078738-84-7

中文名称
——
中文别名
——
英文名称
tert-butyl N-[4-butoxy-3-[[5-[(2-butoxy-5-formylbenzoyl)amino]-2,4-bis(2-methylpropoxy)phenyl]carbamoyl]phenyl]carbamate
英文别名
——
tert-butyl N-[4-butoxy-3-[[5-[(2-butoxy-5-formylbenzoyl)amino]-2,4-bis(2-methylpropoxy)phenyl]carbamoyl]phenyl]carbamate化学式
CAS
1078738-84-7
化学式
C42H57N3O9
mdl
——
分子量
747.929
InChiKey
QJHRWIMVDNQSHA-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):
    8.7
  • 重原子数:
    54
  • 可旋转键数:
    22
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    151
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    tert-butyl N-[4-butoxy-3-[[5-[(2-butoxy-5-formylbenzoyl)amino]-2,4-bis(2-methylpropoxy)phenyl]carbamoyl]phenyl]carbamate三氟乙酸 作用下, 以 氯仿 为溶剂, 反应 1.5h, 以100%的产率得到5,14,26,35-Tetrabutoxy-19,21,40,42-tetrakis(2-methylpropoxy)-2,9,17,23,30,38-hexazaheptacyclo[37.3.1.14,8.111,15.118,22.125,29.132,36]octatetraconta-1(42),4,6,8(48),9,11(47),12,14,18(46),19,21,25,27,29(45),30,32(44),33,35,39(43),40-icosaene-3,16,24,37-tetrone
    参考文献:
    名称:
    Hydrogen Bonding-Directed Multicomponent Dynamic Covalent Assembly of Mono- and Bimacrocycles. Self-Sorting and Macrocycle Exchange
    摘要:
    This paper describes the multicomponent dynamic covalent assembly of macrocyclic structures by utilizing hydrogen bonding-driven zigzag anthranilamides as "leading" components. Two or three amino groups have been introduced to one side of hydrogen bonded anthranilamide oligomers. The preorganization of the frameworks enabled the amino groups to condense with structurally matched aldehydes to form mono- and bimacrocycles in good to quantitative yields. Reactions from Lip to five components have been investigated. which involved one-step formation of up to six imine bonds. The preorganization of the templates highly enhanced the stability of the macrocyclic structures. As a result, all the macrocycles Could be purified by simply recrystallizing the Crude products from suitable solvents. Coexisting experiments of three series of three to five components were also performed, which all revealed that the preorganized precursors possessed high self-sorting capacity. On the basis of the same approach, a hydrazone-based macrocycle was also prepared quantitatively, while an intermacrocycle hydrazone-imine exchange was revealed to facilitate the formation of the hydrazone-based macrocycle from an imine-based macrocycle.
    DOI:
    10.1021/jo801972s
  • 作为产物:
    描述:
    2-butoxy-5-formylbenzoic acid 、 tert-butyl (3-((5-amino-2,4-diisobutoxyphenyl)carbamoyl)-4-butoxyphenyl)carbamate 在 三乙胺氯甲酸异丁酯 作用下, 以 二氯甲烷 为溶剂, 反应 13.0h, 以38%的产率得到tert-butyl N-[4-butoxy-3-[[5-[(2-butoxy-5-formylbenzoyl)amino]-2,4-bis(2-methylpropoxy)phenyl]carbamoyl]phenyl]carbamate
    参考文献:
    名称:
    Hydrogen Bonding-Directed Multicomponent Dynamic Covalent Assembly of Mono- and Bimacrocycles. Self-Sorting and Macrocycle Exchange
    摘要:
    This paper describes the multicomponent dynamic covalent assembly of macrocyclic structures by utilizing hydrogen bonding-driven zigzag anthranilamides as "leading" components. Two or three amino groups have been introduced to one side of hydrogen bonded anthranilamide oligomers. The preorganization of the frameworks enabled the amino groups to condense with structurally matched aldehydes to form mono- and bimacrocycles in good to quantitative yields. Reactions from Lip to five components have been investigated. which involved one-step formation of up to six imine bonds. The preorganization of the templates highly enhanced the stability of the macrocyclic structures. As a result, all the macrocycles Could be purified by simply recrystallizing the Crude products from suitable solvents. Coexisting experiments of three series of three to five components were also performed, which all revealed that the preorganized precursors possessed high self-sorting capacity. On the basis of the same approach, a hydrazone-based macrocycle was also prepared quantitatively, while an intermacrocycle hydrazone-imine exchange was revealed to facilitate the formation of the hydrazone-based macrocycle from an imine-based macrocycle.
    DOI:
    10.1021/jo801972s
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文献信息

  • Hydrogen Bonding-Directed Multicomponent Dynamic Covalent Assembly of Mono- and Bimacrocycles. Self-Sorting and Macrocycle Exchange
    作者:Jian-Bin Lin、Xiao-Na Xu、Xi-Kui Jiang、Zhan-Ting Li
    DOI:10.1021/jo801972s
    日期:2008.12.5
    This paper describes the multicomponent dynamic covalent assembly of macrocyclic structures by utilizing hydrogen bonding-driven zigzag anthranilamides as "leading" components. Two or three amino groups have been introduced to one side of hydrogen bonded anthranilamide oligomers. The preorganization of the frameworks enabled the amino groups to condense with structurally matched aldehydes to form mono- and bimacrocycles in good to quantitative yields. Reactions from Lip to five components have been investigated. which involved one-step formation of up to six imine bonds. The preorganization of the templates highly enhanced the stability of the macrocyclic structures. As a result, all the macrocycles Could be purified by simply recrystallizing the Crude products from suitable solvents. Coexisting experiments of three series of three to five components were also performed, which all revealed that the preorganized precursors possessed high self-sorting capacity. On the basis of the same approach, a hydrazone-based macrocycle was also prepared quantitatively, while an intermacrocycle hydrazone-imine exchange was revealed to facilitate the formation of the hydrazone-based macrocycle from an imine-based macrocycle.
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