3-hydroxymethyl-7,13-diaza-1,4,10-trithiacyclopentadecane-6,14-dione | 343372-27-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酰胺类
• 英文名称: 3-hydroxymethyl-7,13-diaza-1,4,10-trithiacyclopentadecane-6,14-dione
• 英文别名: 2-(Hydroxymethyl)-1,4,10-trithia-7,13-diazacyclopentadecane-6,14-dione
• CAS: 343372-27-0
• 化学式: C₁₁H₂₀N₂O₃S₃
• 分子量: 324.489
• InChiKey: FWORLLVQTIYPRL-UHFFFAOYSA-N

物化性质

• 熔点：
  132-134 °C
• 沸点：
  710.0±60.0 °C(Predicted)
• 密度：
  1.210±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  154
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-hydroxymethyl-7,13-diaza-1,4,10-trithiacyclopentadecane-6,14-dione 在 硼烷四氢呋喃络合物 、 盐酸 作用下， 以 四氢呋喃 为溶剂， 反应 72.0h， 以85%的产率得到1,4,10-三硫杂-7,13-二氮杂环十五碳n-2-基甲醇
  参考文献：
  名称：

  Bis-8-hydroxyquinoline-Armed Diazatrithia-15-crown-5 and Diazatrithia-16-crown-5 Ligands:  Possible Fluorophoric Metal Ion Sensors

  摘要：

  The synthesis and preliminary photophysical properties of a series of diazatrithia-15-crown-5 and diazatrithia-16-crown-5 ligands containing two 8-hydroxyquinoline sidearms are reported. The ligands were prepared by a two-step process. First, diazatrithiacrown ethers 11 and 12 were prepared by treating bis(alpha -chloroamide)5 with various dimercaptans followed by reduction using a boron-THF complex. Hydroxymethyl-substituted macrocycle 12 was rearranged to hydroxysubstituted diazatrithia-16-crown-5 in refluxing aqueous HCl. Macrocyclic diamines 11-13 were converted to either 5-chloro-8-hydroxyquinolin-7-ylmethyl-sudstituted diazatrithiacrown ethers 14-16 by a Mannich aminomethylation reaction or to 8-hydroxyquinolin-2-ylmethyl-substituted diazatrithiacrown ethers 17-19 by reductive amination using 8-hydroxyquinoline-2-carboxaldehyde. Preliminary photophysical studies show that ligands 16 and 19 exhibit increased fluorescence in the presence of Zn2+, indicating that these ligands could be chemical sensors for Zn2+.

  DOI：

  10.1021/jo0017584
• 作为产物：
  描述：

  2,3-二巯基-1-丙醇 、 bis<2-(α-chloroacetamido)ethyl> sulfide 在 potassium carbonate 作用下， 以 乙腈 为溶剂， 反应 48.0h， 以50%的产率得到3-hydroxymethyl-7,13-diaza-1,4,10-trithiacyclopentadecane-6,14-dione
  参考文献：
  名称：

  Bis-8-hydroxyquinoline-Armed Diazatrithia-15-crown-5 and Diazatrithia-16-crown-5 Ligands:  Possible Fluorophoric Metal Ion Sensors

  摘要：

  The synthesis and preliminary photophysical properties of a series of diazatrithia-15-crown-5 and diazatrithia-16-crown-5 ligands containing two 8-hydroxyquinoline sidearms are reported. The ligands were prepared by a two-step process. First, diazatrithiacrown ethers 11 and 12 were prepared by treating bis(alpha -chloroamide)5 with various dimercaptans followed by reduction using a boron-THF complex. Hydroxymethyl-substituted macrocycle 12 was rearranged to hydroxysubstituted diazatrithia-16-crown-5 in refluxing aqueous HCl. Macrocyclic diamines 11-13 were converted to either 5-chloro-8-hydroxyquinolin-7-ylmethyl-sudstituted diazatrithiacrown ethers 14-16 by a Mannich aminomethylation reaction or to 8-hydroxyquinolin-2-ylmethyl-substituted diazatrithiacrown ethers 17-19 by reductive amination using 8-hydroxyquinoline-2-carboxaldehyde. Preliminary photophysical studies show that ligands 16 and 19 exhibit increased fluorescence in the presence of Zn2+, indicating that these ligands could be chemical sensors for Zn2+.

  DOI：

  10.1021/jo0017584

文献信息

• Bis-8-hydroxyquinoline-Armed Diazatrithia-15-crown-5 and Diazatrithia-16-crown-5 Ligands:  Possible Fluorophoric Metal Ion Sensors
  作者：R. Todd Bronson、Jerald S. Bradshaw、Paul B. Savage、Saowarux Fuangswasdi、Sang Chul Lee、Krzysztof E. Krakowiak、Reed M. Izatt

  DOI：10.1021/jo0017584

  日期：2001.7.1

  The synthesis and preliminary photophysical properties of a series of diazatrithia-15-crown-5 and diazatrithia-16-crown-5 ligands containing two 8-hydroxyquinoline sidearms are reported. The ligands were prepared by a two-step process. First, diazatrithiacrown ethers 11 and 12 were prepared by treating bis(alpha -chloroamide)5 with various dimercaptans followed by reduction using a boron-THF complex. Hydroxymethyl-substituted macrocycle 12 was rearranged to hydroxysubstituted diazatrithia-16-crown-5 in refluxing aqueous HCl. Macrocyclic diamines 11-13 were converted to either 5-chloro-8-hydroxyquinolin-7-ylmethyl-sudstituted diazatrithiacrown ethers 14-16 by a Mannich aminomethylation reaction or to 8-hydroxyquinolin-2-ylmethyl-substituted diazatrithiacrown ethers 17-19 by reductive amination using 8-hydroxyquinoline-2-carboxaldehyde. Preliminary photophysical studies show that ligands 16 and 19 exhibit increased fluorescence in the presence of Zn2+, indicating that these ligands could be chemical sensors for Zn2+.