N,N'-bis[4-(methoxymethoxy)benzoyl]-2,6-bis[(6-aminopyrid-2-yl)ethynyl]pyridine | 251640-60-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N,N'-bis[4-(methoxymethoxy)benzoyl]-2,6-bis[(6-aminopyrid-2-yl)ethynyl]pyridine
• 英文别名: 4-(methoxymethoxy)-N-[6-[2-[6-[2-[6-[[4-(methoxymethoxy)benzoyl]amino]pyridin-2-yl]ethynyl]pyridin-2-yl]ethynyl]pyridin-2-yl]benzamide
• CAS: 251640-60-5
• 化学式: C₃₇H₂₉N₅O₆
• 分子量: 639.667
• InChiKey: FRNWBHFYTIOZMM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  48
• 可旋转键数：
  14
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  134
• 氢给体数：
  2
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  N,N'-bis[4-(methoxymethoxy)benzoyl]-2,6-bis[(6-aminopyrid-2-yl)ethynyl]pyridine 在 D(+)-10-樟脑磺酸 作用下， 以 四氢呋喃 、 异丙醇 为溶剂， 反应 4.0h， 以75%的产率得到N,N'-bis(4-hydroxybenzoyl)-2,6-bis[(6-aminopyrid-2-yl)ethynyl]pyridine
  参考文献：
  名称：

  Glucopyranoside Recognition by Polypyridine-Macrocyclic Receptors Possessing a Wide Cavity with a Flexible Linkage

  摘要：

  New polypyridine-macrocyclic receptors for glucopyranosides were designed and synthesized. The artificial receptors possess a terpyridine skeleton asa hydrogen-bonding site and a flexible polyoxyethylene chain as a bridge for the macrocyclic structure, in which the cavity of the receptors is large enough to incorporate pyranosides, The receptors showed high affinities for n-octyl beta-(D)-glucopyranoside, and selective binding of the receptors was observed between epimeric pyranosides. The results obtained in this paper demonstrated versatility of the terpyridine skeleton as a hydrogen-bonding site for saccharides.

  DOI：

  10.1021/jo9911138
• 作为产物：
  描述：

  4-(甲氧基甲基)苯甲酸 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 三氯溴甲烷 、 sodium hydride 、 二乙胺 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 10.17h， 生成 N,N'-bis[4-(methoxymethoxy)benzoyl]-2,6-bis[(6-aminopyrid-2-yl)ethynyl]pyridine
  参考文献：
  名称：

  Glucopyranoside Recognition by Polypyridine-Macrocyclic Receptors Possessing a Wide Cavity with a Flexible Linkage

  摘要：

  New polypyridine-macrocyclic receptors for glucopyranosides were designed and synthesized. The artificial receptors possess a terpyridine skeleton asa hydrogen-bonding site and a flexible polyoxyethylene chain as a bridge for the macrocyclic structure, in which the cavity of the receptors is large enough to incorporate pyranosides, The receptors showed high affinities for n-octyl beta-(D)-glucopyranoside, and selective binding of the receptors was observed between epimeric pyranosides. The results obtained in this paper demonstrated versatility of the terpyridine skeleton as a hydrogen-bonding site for saccharides.

  DOI：

  10.1021/jo9911138

文献信息

• Glucopyranoside Recognition by Polypyridine-Macrocyclic Receptors Possessing a Wide Cavity with a Flexible Linkage
  作者：Masahiko Inouye、Junya Chiba、Hiroyuki Nakazumi

  DOI：10.1021/jo9911138

  日期：1999.10.1

  New polypyridine-macrocyclic receptors for glucopyranosides were designed and synthesized. The artificial receptors possess a terpyridine skeleton asa hydrogen-bonding site and a flexible polyoxyethylene chain as a bridge for the macrocyclic structure, in which the cavity of the receptors is large enough to incorporate pyranosides, The receptors showed high affinities for n-octyl beta-(D)-glucopyranoside, and selective binding of the receptors was observed between epimeric pyranosides. The results obtained in this paper demonstrated versatility of the terpyridine skeleton as a hydrogen-bonding site for saccharides.