Ethyl 2-(carbamoyldiazenyl)cyclohexene-1-carboxylate | 918338-27-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: Ethyl 2-(carbamoyldiazenyl)cyclohexene-1-carboxylate
• CAS: 918338-27-9
• 化学式: C₁₀H₁₅N₃O₃
• 分子量: 225.247
• InChiKey: NSXGSJMHMQHXEL-UHFFFAOYSA-N

物化性质

• 熔点：
  110-112 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
• 沸点：
  346.6±52.0 °C(Predicted)
• 密度：
  1.31±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  94.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  乙酰基乙酰对氯苯胺 、 Ethyl 2-(carbamoyldiazenyl)cyclohexene-1-carboxylate 在 sodium methylate 作用下， 以 四氢呋喃 为溶剂， 以62%的产率得到ethyl 1-[(aminocarbonyl)amino]-3-[(4-chloroanilino)carbonyl]-2-methyl-3a,4,5,6-tetrahydro-1H-3a-indolecarboxylate
  参考文献：
  名称：

  多米诺反应合成新型环烯基-吡咯

  摘要：

  容易获得的环烯基-1-二氮烯和β-二羰基化合物可在一锅中转化为以前未知的不同尺寸的官能化稠合环烯基亚吡咯。多米诺反应通过碱催化的偶联物加成/环化/消除顺序进行。

  DOI：

  10.1016/j.tet.2009.01.040

文献信息

• Zn(II)-Catalyzed Addition of Aromatic/Heteroaromatic C(sp²)–H to Azoalkenes: A Polarity-Reversed Arylation of Carbonyl Compounds
  作者：Cecilia Ciccolini、Lucia De Crescentini、Fabio Mantellini、Stefania Santeusanio、Gianfranco Favi

  DOI：10.1021/acs.orglett.9b01628

  日期：2019.6.7

  An umpolung α-(hetero)arylation strategy that involves the Michael-type reaction between electron-rich (hetero)aromatic substrates and azoalkenes is developed. The reaction proceeds under very mild conditions at room temperature and in the presence of inexpensive, nontoxic ZnCl2 catalyst to provide access to otherwise inaccessible hydrazone structures. Subsequent hydrolysis of these latter to ketones

  提出了一种涉及富电子（杂）芳族底物与偶氮烯烃之间的迈克尔型反应的α-（杂）芳基化反应策略。该反应在非常温和的条件下，在室温下，在廉价，无毒的ZnCl 2催化剂的存在下进行，以提供通向否则无法接近的结构的通道。这些后者随后水解为酮，以及其他有价值的合成转化为各种杂环支架，证明了该方案的实用性。
• Substrate-Controlled Synthesis of Spirocyclopropylpyrazolones and Bicyclic 4,5-Dihydropyrazoles from 1,2-Diaza-1,3-dienes with Sulfur Ylides
  作者：Jiaan Shao、Wenteng Chen、Menghao Zhao、Ke Shu、Huan Liu、Pai Tang

  DOI：10.1021/acs.orglett.8b01562

  日期：2018.7.6

  Substrate-controlled reactions have been developed for the synthesis of spirocyclopropylpyrazolones and bicyclic 4,5-dihydropyrazoles from 1,2-diaza-1,3-dienes and sulfur ylides. These protocols were carried out under mild reaction conditions without any additives in generally moderate to good yields. Plausible mechanisms for the transformations were proposed.

  已经开发了由底物控制的反应，用于由1,2-二氮杂-1,3-二烯和硫酰化物合成螺环丙基丙基吡唑啉酮和双环4,5-二氢吡唑。这些规程是在温和的反应条件下进行的，没有任何添加剂，通常产率中等至良好。提出了可行的转化机制。
• Divergent base-induced reactivity of cycloalkenyl-1-diazenes
  作者：Orazio A. Attanasi、Stefano Berretta、Lucia De Crescentini、Gianfranco Favi、Paolino Filippone、Gianluca Giorgi、Fabio Mantellini

  DOI：10.1016/j.tet.2010.06.061

  日期：2010.8

  The different base-promoted regioselectivities of the ring closure processes in the reactions between cycloalkenyl-1-diazenes and beta-ketoesters are investigated. Under the appropriate conditions it is possible to turn the synthesis towards cycloalkenyliden-pyrroles or functionalized 3-hydroxy-hydrocinnolines. The aromatization procedure of the heteroring counterpart of the 3-hydroxy-hydrocinnolines is also reported. (C) 2010 Elsevier Ltd. All rights reserved.
• Synthesis of Polycyclic Fused Indoline Scaffolds through a Substrate-Guided Reactivity Switch
  作者：Cecilia Ciccolini、Giacomo Mari、Francesco G. Gatti、Giuseppe Gatti、Gianluca Giorgi、Fabio Mantellini、Gianfranco Favi

  DOI：10.1021/acs.joc.0c01489

  日期：2020.9.4

  Zn(II)-catalyzed divergent synthesis of functionalized polycyclic indolines through formal [3 + 2] and [4 + 2] cycloadditions of indoles with 1,2-diaza-1,3-dienes (DDs) is reported. The nature and type of substituents of substrates are found to act as a chemical switch to trigger two distinct reaction pathways and to obtain two different types of products upon the influence of the same catalyst. The mechanism of both [4 + 2] and [3 + 2] cycloadditions was investigated and fully rationalized by density functional theory (DFT) calculations.