N-((tert-butyloxy)carbonyl)-N'-(2-(4-methoxyphenyl)ethyl)-N''-(2-(phenyl)ethyl)iminodiacetic acid diamide | 211745-08-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: N-((tert-butyloxy)carbonyl)-N'-(2-(4-methoxyphenyl)ethyl)-N''-(2-(phenyl)ethyl)iminodiacetic acid diamide
• 英文别名: tert-butyl N-[2-[2-(4-methoxyphenyl)ethylamino]-2-oxoethyl]-N-[2-oxo-2-(2-phenylethylamino)ethyl]carbamate
• CAS: 211745-08-3
• 化学式: C₂₆H₃₅N₃O₅
• 分子量: 469.581
• InChiKey: UZBJYHQJMYZFDM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  34
• 可旋转键数：
  13
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  97
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  N-((tert-butyloxy)carbonyl)-N'-(2-(4-methoxyphenyl)ethyl)-N''-(2-(phenyl)ethyl)iminodiacetic acid diamide 在 盐酸 、 N,N-二异丙基乙胺 、 bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate 作用下， 以 1,4-二氧六环 、 N,N-二甲基甲酰胺 为溶剂， 反应 20.0h， 生成 Bis-{[{[2-(4-methoxy-phenyl)-ethylcarbamoyl]-methyl}-(phenethylcarbamoyl-methyl)-carbamoyl]-methyl}-carbamic acid tert-butyl ester
  参考文献：
  名称：

  溶液相组合合成：通过烯烃易位反应的多样性收敛倍增

  摘要：

  详细介绍了在制备混合物库中，用ω-烯烃官能化的亚氨基二乙酸二酰胺的溶液相合成及其通过烯烃复分解反应的二聚作用。仅由N -BOC-亚氨基二乙酸酐（1），15种胺和4种ω-烯基羧酸说明了可以通过少量单体结构单元的会聚与发散组合实现的多样性，这些单体提供了通常与线性文库合成（包括肽，寡核苷酸和顺序模板功能化。与适合于固相合成技术的此类库的发散合成不同，会聚合成特别适合于溶液相合成，并且由于固相技术通常会在互斥的相中被固相技术排除。

  DOI：

  10.1016/s0040-4020(98)00128-8
• 作为产物：
  描述：

  N-BOC-亚氨基二乙酸 在 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 21.0h， 生成 N-((tert-butyloxy)carbonyl)-N'-(2-(4-methoxyphenyl)ethyl)-N''-(2-(phenyl)ethyl)iminodiacetic acid diamide
  参考文献：
  名称：

  溶液相组合合成：通过烯烃易位反应的多样性收敛倍增

  摘要：

  详细介绍了在制备混合物库中，用ω-烯烃官能化的亚氨基二乙酸二酰胺的溶液相合成及其通过烯烃复分解反应的二聚作用。仅由N -BOC-亚氨基二乙酸酐（1），15种胺和4种ω-烯基羧酸说明了可以通过少量单体结构单元的会聚与发散组合实现的多样性，这些单体提供了通常与线性文库合成（包括肽，寡核苷酸和顺序模板功能化。与适合于固相合成技术的此类库的发散合成不同，会聚合成特别适合于溶液相合成，并且由于固相技术通常会在互斥的相中被固相技术排除。

  DOI：

  10.1016/s0040-4020(98)00128-8

文献信息

• Solution-phase combinatorial synthesis: Convergent multiplication of diversity via the olefin metathesis reaction
  作者：Dale L. Boger、Wenying Chai

  DOI：10.1016/s0040-4020(98)00128-8

  日期：1998.4

  typically associated with linear library syntheses including peptides, oligonucleotides and sequential template functionalizations. Unlike the divergent synthesis of such libraries which is amenable to solid-phase synthesis techniques, the convergent synthesis is especially well suited for solution-phase synthesis and is precluded by solid-phase techniques since the combining components typically would be

  详细介绍了在制备混合物库中，用ω-烯烃官能化的亚氨基二乙酸二酰胺的溶液相合成及其通过烯烃复分解反应的二聚作用。仅由N -BOC-亚氨基二乙酸酐（1），15种胺和4种ω-烯基羧酸说明了可以通过少量单体结构单元的会聚与发散组合实现的多样性，这些单体提供了通常与线性文库合成（包括肽，寡核苷酸和顺序模板功能化。与适合于固相合成技术的此类库的发散合成不同，会聚合成特别适合于溶液相合成，并且由于固相技术通常会在互斥的相中被固相技术排除。
• Higher order iminodiacetic acid libraries for probing protein–protein interactions
  作者：Dale L. Boger、Joel Goldberg、Weiqin Jiang、Wenying Chai、Pierre Ducray、Jae Kyoo Lee、Rachel S. Ozer、Carl-Magnus Andersson

  DOI：10.1016/s0968-0896(98)00128-x

  日期：1998.8

  Full details of the preparation of iminodiacetic acid diamide dimer (2040 compounds), trimer (560 compounds), and tetramer (1596 compounds) libraries by multistep convergent solution-phase synthesis for studying protein-protein interactions are provided. The libraries were assembled in a format providing small 8-10 compound mixtures and the deconvolution of many of the small mixtures to identify screening leads by resynthesis of the individual components have been conducted for 320 of the individual compounds to date. A representative example of the subsequent exploration of the structure-activity relationships for an identified receptor binding antagonist (200 additional individual compounds) and steps taken for potential elaboration to a receptor dimerization agonist are defined with preparation of representative linked dimers (70 compounds). (C) 1998 Elsevier Science Ltd. All rights reserved.
• Convergent Solution-Phase Combinatorial Synthesis with Multiplication of Diversity through Rigid Biaryl and Diarylacetylene Couplings
  作者：Dale L. Boger、Weiqin Jiang、Joel Goldberg

  DOI：10.1021/jo990639p

  日期：1999.9.1

  The solution-phase synthesis of iminodiacetic acid diamide libraries Linked to aryl iodides and their Pd-catalyzed dimerization are detailed. Mixtures containing 64 980 components are synthesized in only 4 steps from N-BOC-iminodiacetic acid anhydride (1) and 21 readily available starting materials, demonstrating the multiplication of diversity achievable by the convergent assembly of building blocks. Both biaryl formation and sequential Stille couplings with bis(tributylstannyl)acetylene are utilized to dimerize the functionalized iminodiacetic acid diamide precursors resulting in product libraries with two sets of binding groups separated by variable length rigid linkers suitable for probing protein-protein interactions. Deconvolution libraries synthesized alongside the full mixtures allow for identification of active components.
• Higher order iminodiacetic acid libraries for probing protein-protein interactions
  作者：Dale L. Boger、Pierre Ducray、Wenying Chai、Weiqin Jiang、Joel Goldberg

  DOI：10.1016/s0960-894x(98)00423-5

  日期：1998.9

  Higher order iminodiacetic acid diamide trimer (560 compounds) and tetramer libraries (1260 compounds) are described and were assembled in a convergent multistep solution-phase synthesis for use in studying protein-protein interactions. (C) 1998 Elsevier Science Ltd. All rights reserved.