6-tertbutyl-diphenylsilanyloxy-hexylamine | 216014-70-9

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: 6-tertbutyl-diphenylsilanyloxy-hexylamine
• 英文别名: 1-(tert-butyldiphenylsilyl)-6-aminohexanol；6-(tert-butyldiphenylsilyloxy)hexan-1-amine；1-O-(tert-butyldiphenylsilanyl)-6-hexylamine；6-amino-1-(t-butyldiphenylsilyloxy)hexane；6-[tert-butyl(diphenyl)silyl]oxyhexan-1-amine
• CAS: 216014-70-9
• 化学式: C₂₂H₃₃NOSi
• 分子量: 355.596
• InChiKey: DHLAIEHPUVIUGD-UHFFFAOYSA-N

物化性质

• 沸点：
  422.7±37.0 °C(Predicted)
• 密度：
  0.98±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.08
• 重原子数：
  25
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  35.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-tertbutyl-diphenylsilanyloxy-hexylamine 在 吡啶 、 四丁基氟化铵 、 三乙胺 作用下， 生成 6-[[14-[2-(Dimethylamino)ethyl]-8-oxo-4,14,15-triazatetracyclo[7.6.1.02,7.013,16]hexadeca-1(15),2(7),3,5,9,11,13(16)-heptaen-10-yl]amino]hexyl methanesulfonate
  参考文献：
  名称：

  Synthesis and biological evaluation of new cytotoxic indazolo[4,3-gh]isoquinolinone derivatives

  摘要：

  A series of indazolo[4,3-gh]isoquinolinones derivatives have been synthesized to decrease cardiotoxic side effects in comparison to Mitoxantrone. The antiproliferative effects of different side chains were investigated and tested on at least four different cell lines of cervix, ovarian, CNS, NSCLC (non-small-cell lung cancer) and colon carcinoma. In addition to antiproliferative activities, influence on cell cycle and intercalation behavior have been tested. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.022
• 作为产物：
  描述：

  (6-azidohexyloxy)(tert-butyl)diphenylsilane 在 2-二苯基膦基苯甲酸 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 2.0h， 以81%的产率得到6-tertbutyl-diphenylsilanyloxy-hexylamine
  参考文献：
  名称：

  三苯基膦羧酰胺：减少叠氮化物的有效试剂及其在核酸检测中的应用

  摘要：

  设计并合成了一系列三苯基膦羧酰胺（TPPc）衍生物，作为三苯基膦的替代试剂，可轻松还原叠氮化物。TPPc衍生物可作为合成伯胺的有效还原剂，而无需其他水解程序。TPPc衍生物还用于在DNA模板荧光反应中使用RhAz-寡核苷酸共轭物进行核酸传感。

  DOI：

  10.1021/ol402832w

文献信息

• Aminoalkyl glucosamine phosphate compounds and their use as adjuvants and immunoeffectors
  申请人：Corixa Corporation

  公开号：US06355257B1

  公开（公告）日：2002-03-12

  Aminoalkyl glucosamine phosphate compounds that are adjuvants and immunoeffectors are described and claimed. The compounds have a 2-deoxy-2-amino glucose in glycosidic linkage with an aminoalkyl (aglycon) group. Compounds are phosphorylated at the 4 or 6 carbon on the glucosamine ring and comprise three 3-alkanoyloxyalkanoyl residues. The compounds augment antibody production in immunized animals as well as stimulate cytokine production and activate macrophages. Methods for using the compounds as adjuvants and immunoeffectors are also disclosed.

  描述和声明了一种氨基糖胺磷酸盐化合物，它们是辅助剂和免疫效应物质。这些化合物具有一个2-脱氧-2-氨基葡萄糖与一个氨基烷基（非糖部分）基团的糖苷键连接。这些化合物在葡萄糖胺环上的4或6碳上磷酸化，并包括三个3-烷酰氧烷酰残基。这些化合物增强了免疫动物中的抗体产生，同时刺激细胞因子的产生并激活巨噬细胞。还公开了将这些化合物用作辅助剂和免疫效应物质的方法。
• A New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride-<i>N</i>-Methylimidazole-Iodine
  作者：Jacek Stawinski、Agnieszka Bartoszewicz、Marcin Kalek、Johan Nilsson、Renata Hiresova

  DOI：10.1055/s-2007-992379

  日期：2008.1

  reactions of alcohols with silyl chlorides in the presence of N-methylimidazole were significantly accelerated by the added iodine, and on this basis a general, and high yielding method for efficient silylation of primary, secondary, and tertiary alcohols was developed.

  发现在N-甲基咪唑存在下醇与甲硅烷基氯的反应通过加入碘显着加速，并在此基础上开发了一种通用的、高收率的伯、仲和叔醇的有效硅烷化方法。
• Synthesis and anti-HIV-1 integrase activity of modified dinucleotides
  作者：Yves Aubert、Marcel Chassignol、Victoria Roig、Gladys Mbemba、Julien Weiss、Hervé Meudal、Jean-François Mouscadet、Ulysse Asseline

  DOI：10.1016/j.ejmech.2009.09.007

  日期：2009.12

  The synthesis of a series of thirty-eight new modified dinucleotides and dinucleotide conjugate analogues of d-5′ApC3′ is described. The inhibitory activity of these compounds toward HIV-1 integrase was examined in enzymatic assays using the natural dinucleotide as a reference. Among the compounds, a perylene-dinucleotide conjugate has shown a two micromolar anti-integrase activity due to the presence

  一系列38新型改性二核苷酸和D-的二核苷酸偶联物类似物的合成5' APC 3'进行说明。这些酶对HIV-1整合酶的抑制活性在酶法测定中以天然二核苷酸为参考进行了检测。在这些化合物中，由于嵌入剂和二核苷酸的存在，a-二核苷酸缀合物具有两个微摩尔的抗整合酶活性。
• Self-Assembly of Stimuli-Responsive [2]Rotaxanes by Amidinium Exchange
  作者：Oleg Borodin、Yevhenii Shchukin、Craig C. Robertson、Stefan Richter、Max von Delius

  DOI：10.1021/jacs.1c05230

  日期：2021.10.13

  of an underexplored dynamic covalent reaction for the synthesis of stimuli-responsive [2]rotaxanes. The formamidinium moiety lies at the heart of these mechanically interlocked architectures, because it enables both dynamic covalent exchange and the binding of simple crown ethers. We demonstrated that the rotaxane self-assembly follows a unique reaction pathway and that the complex interplay between

  超分子化学的进步通常以基础构件和实现其相互转化的方法的发展为基础。在这项工作中，我们报告了使用未经充分探索的动态共价反应来合成刺激响应性[2]轮烷。甲脒部分位于这些机械联锁结构的核心，因为它能够实现动态共价交换和简单冠醚的结合。我们证明了轮烷自组装遵循独特的反应途径，并且冠醚和线之间复杂的相互作用可以通过添加碱和燃料酸以瞬时方式控制。当动态组合文库暴露于不同的亲核试剂时，揭示了机械键的深远稳定作用以及看似相似的[2]轮烷之间有趣的反应性差异。
• Aminoalkyl glucosaminide phosphate compounds and their use as adjuvants and immunoeffectors
  申请人：Corixa Corporation

  公开号：US20030199460A1

  公开（公告）日：2003-10-23

  Aminoalkyl glucosaminide phosphate (AGP) compounds that are adjuvants and immunoeffectors are described and claimed. The compounds have a 2-deoxy-2-amino glucose in glycosidic linkage with an aminoalkyl (aglycon) group. Compounds are phosphorylated at the 4 or 6 carbon on the glucosaminide ring and comprise three 3-alkanoyloxyalkanoyl residues. The compounds augment antibody production in immunized animals as well as stimulate cytokine production and activate macrophages. Compositions and methods for using the compounds as adjuvants and immunoeffectors are also disclosed.

  本文描述并声明了一种作为佐剂和免疫效应物的氨基糖脂磷酸酯（AGP）化合物。该化合物具有一个2-脱氧-2-氨基葡萄糖与一个氨基烷基（缺糖基团）组成的糖苷键。该化合物在葡萄糖氨基环上的4或6碳上磷酸化，并包含三个3-烷酰氧基烷酰基残基。该化合物增强了免疫动物中的抗体产生，并刺激细胞因子的产生和激活巨噬细胞。本文还公开了使用该化合物作为佐剂和免疫效应物的组合物和方法。