1-((3s,5s,7s)-adamantan-1-yl)-1H-benzo[d][1,2,3]triazole | 83610-26-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并三唑类
• 英文名称: 1-((3s,5s,7s)-adamantan-1-yl)-1H-benzo[d][1,2,3]triazole
• 英文别名: 1-(1-adamantyl)-1H-benzo[d][1,2,3]triazole；1-(1-adamantyl)-1,2,3-benzotriazole；1-(1-adamantyl)benzotriazole；Cambridge id 5635285
• CAS: 83610-26-8
• 化学式: C₁₆H₁₉N₃
• 分子量: 253.347
• InChiKey: PYJPJZUMUCRLJK-UHFFFAOYSA-N

物化性质

• 熔点：
  149-151 °C
• 沸点：
  420.1±14.0 °C(Predicted)
• 密度：
  1.46±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  30.7
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  T406石油添加剂 、 金刚烷 在 aluminum tri-bromide 、 四溴化碳 作用下， 以 neat (no solvent) 为溶剂， 反应 0.08h， 以91%的产率得到1-((3s,5s,7s)-adamantan-1-yl)-1H-benzo[d][1,2,3]triazole
  参考文献：
  名称：

  Solvent-free and direct C(sp3)–H amination of adamantanes by grinding

  摘要：

  A facile, direct and environmentally benign conversion of C(sp(3))-H bonds to C(sp(3))-N bonds using substoichiometric amount of aprotic superelectrophiles polyhalomethane-AIX(3) has been achieved by grinding under solvent-free conditions at room temperature in air. It is a general and simple method for the direct amination of adamantanes, and a series of aminoadamantanes of azoles, arylamines or heteroarylamines were obtained in good to excellent yields. The advantages of this amination are atom economy, solvent-free, chemoselectivity, short reaction time and high yields. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.01.014

文献信息

• Benzyne Click Chemistry: Synthesis of Benzotriazoles from Benzynes and Azides
  作者：Feng Shi、Jesse P. Waldo、Yu Chen、Richard C. Larock

  DOI：10.1021/ol800675u

  日期：2008.6.1

  A variety of substituted benzotriazoles have been prepared by the [3 + 2] cycloaddition of azides to benzynes. The reaction scope is quite general, affording a rapid and easy entry to substituted, functionalized benzotriazoles under mild conditions.

  多种取代的苯并三唑已通过叠氮化物与苄的 [3 + 2] 环加成反应制备。反应范围非常广泛，可以在温和的条件下快速轻松地获得取代的、官能化的苯并三唑。
• Synthesis of adamantane derivatives. LVIII. Reaction of 1-adamantyl chloride with some heterocyclic unsaturated silanes.
  作者：TADASHI SASAKI、AKIRA NAKANISHI、MASATOMI OHNO

  DOI：10.1248/cpb.30.2051

  日期：——

  Various silylated heterocycles having amide functionality were treated with 1-adamantyl chloride (1) in the presence of a Lewis acid to give the corresponding N-adamantylated heterocycles. If α-position to the reacting lactim nitrogen was substituted, the reaction no longer occurred, or the adamantylation occurred at the position other than the expected nitrogen. These facts are attributed to a steric blocking effect of the α-substituent. While the same treatment of the thioamide 46 gave the S-adamantylated product, 48 and 51 afforded in contrast the N- and S-adamantylated products, respectively ; this result can be explained in terms of steric effect. Analogously, silylated 2-pyrazolines and triazoles were adamantylated at nitrogen. The reactions of 2-trimethylsilylthiophene, furan and -pyridine with 1 failed to give site-selective monoadamantylation.

  在路易斯酸存在下，用 1-金刚烷酰氯（1）处理各种具有酰胺官能团的硅烷化杂环，得到相应的 N-金刚烷化杂环。如果反应的内酰胺氮的α位被取代，则不再发生反应，或者在预期氮以外的位置发生金刚烷基化反应。这些情况都归因于 α 取代基的立体阻滞效应。同样处理硫代酰胺 46 得到的是 S-金刚烷化产物，而 48 和 51 则分别得到了 N-和 S-金刚烷化产物；这一结果可以用立体效应来解释。类似地，硅烷化的 2-吡唑和三唑也在氮处发生了金刚烷化。2-三甲基硅基噻吩、呋喃和吡啶与 1 的反应未能产生位点选择性的单金刚烷化反应。
• Gonzalez; Alarcon; Cabildo, European Journal of Medicinal Chemistry, 1985, vol. 20, # 4, p. 359 - 362
  作者：Gonzalez、Alarcon、Cabildo、et al.

  DOI：——

  日期：——
• ——
  作者：V. G. Tsypin、M. S. Pevzner、E. L. Golod

  DOI：10.1023/a:1013938527863

  日期：——

  A procedure has been developed for oxidative N-adamantylation of azoles with 1-iodoadamantane in the presence of chromium(IV) oxide or iodine(V) oxide. The procedure is applicable to azoles whose pK(BH+) value does not exceed 2.26.
• GONZALEZ, M. E.;ALARCON, B.;CABILDO, P.;CLARAMUNT, R. M.;SANZ, D.;ELGUERO+, EUR. J. MED. CHEM., 1985, 20, N 4, 359-362
  作者：GONZALEZ, M. E.、ALARCON, B.、CABILDO, P.、CLARAMUNT, R. M.、SANZ, D.、ELGUERO+

  DOI：——

  日期：——