[[2-(2-{(2-tert-Butoxycarbonylamino-ethyl)-[2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetylamino)-ethyl]-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid allyl ester | 289684-59-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: [[2-(2-{(2-tert-Butoxycarbonylamino-ethyl)-[2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetylamino)-ethyl]-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid allyl ester
• 英文别名: prop-2-enyl 2-[9H-fluoren-9-ylmethoxycarbonyl-[2-[[2-[[2-[2-(2-methylpropanoylamino)-6-oxo-1H-purin-9-yl]acetyl]-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]amino]acetyl]amino]ethyl]amino]acetate
• CAS: 289684-59-9
• 化学式: C₄₂H₅₁N₉O₁₀
• 分子量: 841.921
• InChiKey: OFWVUESZVQBAME-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  61
• 可旋转键数：
  22
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  232
• 氢给体数：
  4
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  [[2-(2-{(2-tert-Butoxycarbonylamino-ethyl)-[2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetylamino)-ethyl]-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid allyl ester 在 bis-triphenylphosphine-palladium(II) chloride 哌啶 、 三正丁基氢锡 、 溶剂黄146 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 生成 N-[9-[2-(3,9-dioxo-1,4,7,10-tetrazacyclododec-1-yl)-2-oxoethyl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide
  参考文献：
  名称：

  An expeditious liquid-phase synthesis of cyclic peptide nucleic acids

  摘要：

  Suitably protected linear precursors of cyclic PNAs can be readily obtained by BOP/DiPEA coupling of the corresponding sub-monomers. Conversion of the linear PNA dimers into the pentafluorophenyl esters allows cyclization by intramolecular attack of the deprotected primary amino function under diluted conditions. After removal of the secondary amino protecting group(s), installation of the required nucleobase-acetyl function(s) affords cyclic PNAs. In addition, the latter compounds can be prepared following a direct coupling strategy. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(00)00536-0
• 作为产物：
  描述：

  [(2-Amino-ethyl)-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid allyl ester 、 N-[2-(tert-butoxycarbonyl)aminoethyl]-N-[[2-N-(isobutyryl)guanin-9-yl]acetyl]glycine 在 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以75%的产率得到[[2-(2-{(2-tert-Butoxycarbonylamino-ethyl)-[2-(2-isobutyrylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetylamino)-ethyl]-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid allyl ester
  参考文献：
  名称：

  An expeditious liquid-phase synthesis of cyclic peptide nucleic acids

  摘要：

  Suitably protected linear precursors of cyclic PNAs can be readily obtained by BOP/DiPEA coupling of the corresponding sub-monomers. Conversion of the linear PNA dimers into the pentafluorophenyl esters allows cyclization by intramolecular attack of the deprotected primary amino function under diluted conditions. After removal of the secondary amino protecting group(s), installation of the required nucleobase-acetyl function(s) affords cyclic PNAs. In addition, the latter compounds can be prepared following a direct coupling strategy. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(00)00536-0

文献信息

• An expeditious liquid-phase synthesis of cyclic peptide nucleic acids
  作者：Jeroen C Verheijen、Gijsbert M Grotenbreg、Ludo Hart de Ruyter、Pieter A.M van der Klein、Gijsbert A van der Marel、Jacques H van Boom

  DOI：10.1016/s0040-4039(00)00536-0

  日期：2000.5

  Suitably protected linear precursors of cyclic PNAs can be readily obtained by BOP/DiPEA coupling of the corresponding sub-monomers. Conversion of the linear PNA dimers into the pentafluorophenyl esters allows cyclization by intramolecular attack of the deprotected primary amino function under diluted conditions. After removal of the secondary amino protecting group(s), installation of the required nucleobase-acetyl function(s) affords cyclic PNAs. In addition, the latter compounds can be prepared following a direct coupling strategy. (C) 2000 Elsevier Science Ltd. All rights reserved.