4-(2-{2-[2-(2-Azido-ethoxy)-ethoxy]-ethoxy}-ethyl)-morpholine-2,6-dione | 239081-43-7

• 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: 4-(2-{2-[2-(2-Azido-ethoxy)-ethoxy]-ethoxy}-ethyl)-morpholine-2,6-dione
• 英文别名: 4-[2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]ethyl]morpholine-2,6-dione；4-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]morpholine-2,6-dione
• CAS: 239081-43-7
• 化学式: C₁₂H₂₀N₄O₆
• 分子量: 316.314
• InChiKey: ZPTWKTODUDCKNO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  22
• 可旋转键数：
  12
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  88.7
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  4-(2-{2-[2-(2-Azido-ethoxy)-ethoxy]-ethoxy}-ethyl)-morpholine-2,6-dione 在 苯硫酚 、 三乙胺 、 tin(ll) chloride 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 12.0h， 生成 (S)-22-((allyloxy)carbonyl)-3-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)-5,19,24-trioxo-9,12,15,25-tetraoxa-3,6,18,23-tetraazaoctacos-27-enoic acid
  参考文献：
  名称：

  Reduction of Azides to Primary Amines in Substrates Bearing Labile Ester Functionality. Synthesis of a PEG-Solubilized, “Y”-Shaped Iminodiacetic Acid Reagent for Preparation of Folate-Tethered Drugs¹

  摘要：

  Anhydride 3 is a useful reagent for the synthesis of triply linked drug conjugates. Examples using paclitaxel are provided. Conversion of the azido moiety to a primary amine in the presence of substrates bearing labile ester functionality requires the use of a tin/mercaptan reducing system which includes methanol exchange equilibration to effect nitrogen-tin bond scission.

  DOI：

  10.1021/ol9905248
• 作为产物：
  描述：

  1-氨基-11-叠氮-3,6,9-三氧杂十一烷 在 四(三苯基膦)钯 苯硅烷 、 potassium carbonate 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 36.0h， 生成 4-(2-{2-[2-(2-Azido-ethoxy)-ethoxy]-ethoxy}-ethyl)-morpholine-2,6-dione
  参考文献：
  名称：

  Synthesis and Evaluation of Taxol–Folic Acid Conjugates as Targeted Antineoplastics † †See ref 1.

  摘要：

  A series of Taxol derivatives tethered at C2' and C-7 to glutamate and folate have been synthesized for evaluation as prodrugs which release Taxol via hydrolytic lability of their alpha-alkoxy and alpha-amino esters. The half-time for hydrolysis of these materials was determined in pH 7 and pH 5 buffer. The in vitro cytotoxicity has been assessed in cell culture against A-549 lung cancer, MCF-7 breast cancer, and HT-29 colon cancer. Selected agents were further screened for folate binding and competitive binding with free folic acid, One agent (54), further evaluated in animal Studies as found to increase the lifespan in mice, but was less effective than Taxol itself. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(02)00019-6

文献信息

• Synthesis and Evaluation of Taxol–Folic Acid Conjugates as Targeted Antineoplastics † †See ref 1.
  作者：Jae Wook Lee、June Y Lu、P.S Low、P.L Fuchs

  DOI：10.1016/s0968-0896(02)00019-6

  日期：2002.7

  A series of Taxol derivatives tethered at C2' and C-7 to glutamate and folate have been synthesized for evaluation as prodrugs which release Taxol via hydrolytic lability of their alpha-alkoxy and alpha-amino esters. The half-time for hydrolysis of these materials was determined in pH 7 and pH 5 buffer. The in vitro cytotoxicity has been assessed in cell culture against A-549 lung cancer, MCF-7 breast cancer, and HT-29 colon cancer. Selected agents were further screened for folate binding and competitive binding with free folic acid, One agent (54), further evaluated in animal Studies as found to increase the lifespan in mice, but was less effective than Taxol itself. (C) 2002 Elsevier Science Ltd. All rights reserved.
• Reduction of Azides to Primary Amines in Substrates Bearing Labile Ester Functionality. Synthesis of a PEG-Solubilized, “Y”-Shaped Iminodiacetic Acid Reagent for Preparation of Folate-Tethered Drugs¹
  作者：Jae Wook Lee、Philip L. Fuchs

  DOI：10.1021/ol9905248

  日期：1999.7.1

  Anhydride 3 is a useful reagent for the synthesis of triply linked drug conjugates. Examples using paclitaxel are provided. Conversion of the azido moiety to a primary amine in the presence of substrates bearing labile ester functionality requires the use of a tin/mercaptan reducing system which includes methanol exchange equilibration to effect nitrogen-tin bond scission.