2-[3-(furan-2-ylmethoxy)-2-hydroxy-propoxy]-isoindole-1,3-dione | 859214-67-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 2-[3-(furan-2-ylmethoxy)-2-hydroxy-propoxy]-isoindole-1,3-dione
• CAS: 859214-67-8
• 化学式: C₁₆H₁₅NO₆
• 分子量: 317.298
• InChiKey: RGYWAEXFHMNNPA-NSHDSACASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.38
• 重原子数：
  23.0
• 可旋转键数：
  7.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  89.21
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  2-[3-(furan-2-ylmethoxy)-2-hydroxy-propoxy]-isoindole-1,3-dione 在 PS-diethylenetriamine 、 溶剂黄146 作用下， 以 二氯甲烷 、 乙酸乙酯 为溶剂， 生成 Acetic acid (2R,3S,6R)-2-acetoxymethyl-6-{2-[(S)-3-(furan-2-ylmethoxy)-2-hydroxy-propoxyimino]-ethyl}-3,6-dihydro-2H-pyran-3-yl ester
  参考文献：
  名称：

  Convergent Synthesis of a Complex Oxime Library Using Chemical Domain Shuffling

  摘要：

  yThe synthesis of a complex hybrid oxime library is reported utilizing convergent ligation of alkoxyamine and carbonyl monomers via "chemical domain shuffling". Initial biological screening of the library against human small cell lung carcinoma (A549) cells led to the identification of a novel hybrid dimer in contrast to the corresponding monomeric compounds which were found to be inactive.

  DOI：

  10.1021/ol051023r
• 作为产物：
  描述：

  (S)-2-((oxiran-2-ylmethoxy)methyl)furan 、 N-羟基邻苯二甲酰亚胺 在 chiral salen-based cobalt 、 lutidinium p-toluenesulfonate 作用下， 以 四氢呋喃 为溶剂， 反应 16.0h， 以95%的产率得到2-[3-(furan-2-ylmethoxy)-2-hydroxy-propoxy]-isoindole-1,3-dione
  参考文献：
  名称：

  Stereocontrolled Synthesis of a Complex Library via Elaboration of Angular Epoxyquinol Scaffolds

  摘要：

  We have accomplished the synthesis of a complex chemical library via elaboration of angular epoxyquinol scaffolds with distinct skeletal frameworks. The key strategy involves highly stereocontrolled [4 + 2] Diels-Alder cycloadditions of chiral, nonracemic epoxyquinol dienes to generate the scaffolds. Further scaffold diversification involves hydrogenation, epimerization, dehydration, and condensation of the carbonyl group with alkoxyamine and carbazate building blocks. Further elaboration of the scaffolds also provided new skeletal frameworks using hydroxyl-directed Diels-Alder cycloaddition and reductive N-N bond cleavage. The overall process afforded 244 highly complex and functionalized compounds. Preliminary biological screening of the library uncovered six compounds which showed significant inhibition of Hsp 72 induction.

  DOI：

  10.1021/jo050956y