2-Bromomethyl-6,10-dimethyl-triphenylene | 239455-01-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: 2-Bromomethyl-6,10-dimethyl-triphenylene
• 英文别名: 2-(Bromomethyl)-6,10-dimethyltriphenylene
• CAS: 239455-01-7
• 化学式: C₂₁H₁₇Br
• 分子量: 349.27
• InChiKey: IKSCLAVFUNXRFY-UHFFFAOYSA-N

物化性质

• 沸点：
  524.4±19.0 °C(Predicted)
• 密度：
  1.375±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  2-Bromomethyl-6,10-dimethyl-triphenylene 在 lithium copper bromide 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 为溶剂， 生成 1-[5-(6,10-Dimethyltriphenylen-2-yl)pentyl]pyrrolidine-2,5-dione
  参考文献：
  名称：

  A possible improvement for structure-based drug design illustrated by the discovery of a Tat HIV-1 inhibitor

  摘要：

  The HIV-1 Tat protein is a promising target for AIDS therapy, due to its extra-cellular roles against the immune system. From the 2D-NMR structure of Tat, we have designed molecules, called TDS, able to bind to Tat and inhibit HIV-1 replication in vitro. This new family of antivirals is composed of a triphenylene aromatic ring substituted with at least one carbon chain bearing a succinimide group. These ligands are prepared from triphenylene or 2,6, 10-trimethylphenylene in 3-6 steps depending on the target molecule. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.095
• 作为产物：
  描述：

  2,6,10-trimethyltriphenylene 在 N-溴代丁二酰亚胺(NBS) 、 偶氮二异丁腈 、 过氧化苯甲酰 作用下， 以 四氯化碳 为溶剂， 以40%的产率得到2-Bromomethyl-6,10-dimethyl-triphenylene
  参考文献：
  名称：

  A possible improvement for structure-based drug design illustrated by the discovery of a Tat HIV-1 inhibitor

  摘要：

  The HIV-1 Tat protein is a promising target for AIDS therapy, due to its extra-cellular roles against the immune system. From the 2D-NMR structure of Tat, we have designed molecules, called TDS, able to bind to Tat and inhibit HIV-1 replication in vitro. This new family of antivirals is composed of a triphenylene aromatic ring substituted with at least one carbon chain bearing a succinimide group. These ligands are prepared from triphenylene or 2,6, 10-trimethylphenylene in 3-6 steps depending on the target molecule. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.095