3-chloromethyl-2-methyl-5-(1',2',3',4'-tetra-O-tert-butyldimethylsilyl-D-arabino-tetritol-1'-yl)furan | 551937-28-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: 3-chloromethyl-2-methyl-5-(1',2',3',4'-tetra-O-tert-butyldimethylsilyl-D-arabino-tetritol-1'-yl)furan
• 英文别名: tert-butyl-dimethyl-[(1S,2R,3R)-1,3,4-tris[[tert-butyl(dimethyl)silyl]oxy]-1-[4-(chloromethyl)-5-methylfuran-2-yl]butan-2-yl]oxysilane
• CAS: 551937-28-1
• 化学式: C₃₄H₇₁ClO₅Si₄
• 分子量: 707.73
• InChiKey: NULYMORZCVUZQP-IDZRBWSNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12.19
• 重原子数：
  44
• 可旋转键数：
  17
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  50.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-chloromethyl-2-methyl-5-(1',2',3',4'-tetra-O-tert-butyldimethylsilyl-D-arabino-tetritol-1'-yl)furan 在 吡啶 、 4 A molecular sieve 、 sodium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 8.0h， 生成 5-[4'-[N-acetyl-N-[2-methyl-5-(1',2',3',4'-tetra-O-tert-butyldimethylsilyl-D-arabino-tetritol-1'-yl)furan-3-ylmethyl]amino]-1',2',3'-tri-O-tert-butyldimetylsilyl-4'-deoxy-D-arabino-tetritol-1'-yl]-3-ethoxycarbonyl-2-methylfuran
  参考文献：
  名称：

  Hetaryleneaminopolyols and Hetarylenecarbopeptoids:  a New Type of Glyco- and Peptidomimetics. Syntheses and Studies on Solution Conformation and Dynamics

  摘要：

  Ready access to a new class of oligomers has been demonstrated by the synthesis of hetarylene-aminopolyols and hetarylenecarbopeptoids using 3-hydroxymethyl-5-(4-amino-4-deoxy-D-arabinotetritol-1-yl)-2-methylfuran and 5-(4-amino-4-deoxy-D-arabinotetritol-1-yl)-2-methyl-3-furoic acid as novel scaffolds. The conformational behavior of peptidomimetics 22, 23, 25, 26, and 36 have been analyzed by NMR spectroscopy and extensive molecular dynamics simulations. MD simulations using the GB/SA continuum solvent model for water and the MM3* force field provide a population distribution of conformers which satisfactorily agrees with the experimental NMR data for the torsional degrees of freedom of the molecule.

  DOI：

  10.1021/jo026631o
• 作为产物：
  描述：

  ethyl 2-methyl-5-(D-arabino-tetritol-1-yl)furan-3-carboxylate 在 咪唑 、 四氯化碳 、 lithium aluminium tetrahydride 、 4 A molecular sieve 、 三苯基膦 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 18.25h， 生成 3-chloromethyl-2-methyl-5-(1',2',3',4'-tetra-O-tert-butyldimethylsilyl-D-arabino-tetritol-1'-yl)furan
  参考文献：
  名称：

  Hetaryleneaminopolyols and Hetarylenecarbopeptoids:  a New Type of Glyco- and Peptidomimetics. Syntheses and Studies on Solution Conformation and Dynamics

  摘要：

  Ready access to a new class of oligomers has been demonstrated by the synthesis of hetarylene-aminopolyols and hetarylenecarbopeptoids using 3-hydroxymethyl-5-(4-amino-4-deoxy-D-arabinotetritol-1-yl)-2-methylfuran and 5-(4-amino-4-deoxy-D-arabinotetritol-1-yl)-2-methyl-3-furoic acid as novel scaffolds. The conformational behavior of peptidomimetics 22, 23, 25, 26, and 36 have been analyzed by NMR spectroscopy and extensive molecular dynamics simulations. MD simulations using the GB/SA continuum solvent model for water and the MM3* force field provide a population distribution of conformers which satisfactorily agrees with the experimental NMR data for the torsional degrees of freedom of the molecule.

  DOI：

  10.1021/jo026631o