2--4-(benzyloxy)-1-bromonaphthalene | 157528-12-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2--4-(benzyloxy)-1-bromonaphthalene
• 英文别名: tert-butyl N-(1-bromo-4-phenylmethoxynaphthalen-2-yl)-N-methylcarbamate
• CAS: 157528-12-6
• 化学式: C₂₃H₂₄BrNO₃
• 分子量: 442.352
• InChiKey: NITMYIMWIVBQMY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  38.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2--4-(benzyloxy)-1-bromonaphthalene 在 palladium on activated charcoal 4-二甲氨基吡啶 、 lithium hydroxide 、 sodium tetrahydroborate 、 正丁基锂 、 氢气 、 三氟乙酸 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙醇 、 二氯甲烷 为溶剂， 反应 2.0h， 生成 2-(甲基氨基)萘-1,4-二酮
  参考文献：
  名称：

  p-Quinonemethide Analog of the CC-1065 and Duocarmycin Alkylation Subunits

  摘要：

  The synthesis and preliminary evaluation of 10 and 11, stable precursors to the inherently reactive but isolable p-quinonemethide analog 9 of the CC-1065 and duocarmycin alkylation subunits, are detailed. The p-quinonemethide 9, while reactive (t(1/2) < 1 min, CH3OH), represents one of the few unsubstituted quinonemethides sufficiently stable for isolation and characterization. The structural origin of this stability and the ramifications of the observations on the origin of the stability of the CC-1065 and duocarmycin alkylation subunits are discussed.

  DOI：

  10.1021/jo00096a043
• 作为产物：
  描述：

  N-(tert-butyloxycarbonyl)-4-(benzyloxy)-2-naphthylamine 在 N-溴代丁二酰亚胺(NBS) 、 硫酸 、 sodium hydride 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 7.58h， 生成 2--4-(benzyloxy)-1-bromonaphthalene
  参考文献：
  名称：

  p-Quinonemethide Analog of the CC-1065 and Duocarmycin Alkylation Subunits

  摘要：

  The synthesis and preliminary evaluation of 10 and 11, stable precursors to the inherently reactive but isolable p-quinonemethide analog 9 of the CC-1065 and duocarmycin alkylation subunits, are detailed. The p-quinonemethide 9, while reactive (t(1/2) < 1 min, CH3OH), represents one of the few unsubstituted quinonemethides sufficiently stable for isolation and characterization. The structural origin of this stability and the ramifications of the observations on the origin of the stability of the CC-1065 and duocarmycin alkylation subunits are discussed.

  DOI：

  10.1021/jo00096a043

文献信息

• p-Quinonemethide Analog of the CC-1065 and Duocarmycin Alkylation Subunits
  作者：Dale L. Boger、Takahide Nishi、Bradley R. Teegarden

  DOI：10.1021/jo00096a043

  日期：1994.8

  The synthesis and preliminary evaluation of 10 and 11, stable precursors to the inherently reactive but isolable p-quinonemethide analog 9 of the CC-1065 and duocarmycin alkylation subunits, are detailed. The p-quinonemethide 9, while reactive (t(1/2) < 1 min, CH3OH), represents one of the few unsubstituted quinonemethides sufficiently stable for isolation and characterization. The structural origin of this stability and the ramifications of the observations on the origin of the stability of the CC-1065 and duocarmycin alkylation subunits are discussed.