(1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexanamine | 764650-92-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: (1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexanamine
• 英文别名: (1R,2R)-2-(2-methyl-5-phenyl-pyrrol-1-yl)cyclohexylamine；(R,R)-2-(2-methyl-5-phenyl-pyrrol-1-yl)-cyclohexylamine；(R,R)-2-(2-methyl-5-phenylpyrrol-1-yl)cyclohexylamine
• CAS: 764650-92-2
• 化学式: C₁₇H₂₂N₂
• 分子量: 254.375
• InChiKey: HXDGOJZAAUBGPA-NVXWUHKLSA-N

物化性质

• 沸点：
  401.5±45.0 °C(Predicted)
• 密度：
  1.11±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.91
• 重原子数：
  19.0
• 可旋转键数：
  2.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  30.95
• 氢给体数：
  1.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  (S)-2-isothiocyanato-N,N-diethyl-3,3-dimethylbutanamide 、 (1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexanamine 以 二氯甲烷 为溶剂， 以340 mg的产率得到(S)-N,N-diethyl-3,3-dimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-pyrrol-1-yl)cyclohexyl)thioureido)butanamide
  参考文献：
  名称：

  Organocatalytic Asymmetric Transfer Hydrogenation of Nitroolefins

  摘要：

  We describe a highly efficient and highly enantioselective Hantzsch ester mediated conjugate transfer hydrogenation of beta,beta-disubstituted nitroolefins that is catalyzed by a Jacobsen-type thiourea catalyst.

  DOI：

  10.1021/ja074045c
• 作为产物：
  描述：

  1-苯基-1,4-戊二酮 、 (1R,2R)-1,2-diaminocyclohexane 在 溶剂黄146 作用下， 以 甲醇 为溶剂， 以70%的产率得到(1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexanamine
  参考文献：
  名称：

  羟基内酰胺的对映选择性 Pictet-Spengler 型环化：阴离子结合的 H 键供体催化

  摘要：

  在硫脲催化的色胺衍生的羟基内酰胺的环化中获得高度对映体富集的吲哚嗪酮和喹嗪酮产物。取代基和反离子效应研究指出了一种新的催化机制，涉及限速阴离子提取和硫脲结合。

  DOI：

  10.1021/ja076179w

文献信息

• Regio- and Enantioselective Catalytic Cyclization of Pyrroles onto <i>N</i>-Acyliminium Ions
  作者：Izzat T. Raheem、Parvinder S. Thiara、Eric N. Jacobsen

  DOI：10.1021/ol800256j

  日期：2008.4.1

  The regio- and enantioselective cyclization of pyrroles onto N-acyliminium ions generated in situ from hydroxylactams is reported. Modest to excellent ee's and yields are obtained in these novel Pictet-Spengler-type reactions with a chiral thiourea-pyrrole catalyst. Useful synthetic transformations of the versatile pyrroloindolizidinone and pyrroloquinolizidinone products are presented.

  报道了吡咯在由羟基内酰胺原位产生的N-酰亚胺离子上的区域和对映体选择性环化。用手性硫脲-吡咯催化剂在这些新颖的Pictet-Spengler型反应中获得中等至优异的ee和收率。提出了通用的吡咯并吲哚并din啶酮和吡咯并喹啉并din啶酮产物的有用的合成转化。
• Plagiarizing Proteins: Enhancing Efficiency in Asymmetric Hydrogen-Bonding Catalysis through Positive Cooperativity
  作者：Christopher R. Jones、G. Dan Pantoş、Angus J. Morrison、Martin D. Smith

  DOI：10.1002/anie.200903063

  日期：2009.9.21

  A new twist for a fold: Conformationally well‐defined thiourea catalysts, like that shown, stabilized by intramolecular hydrogen bonds demonstrate cooperative ligand–receptor binding. This conformation leads to significantly enhanced catalytic efficiency, resulting in higher turnover rates and lower catalyst loading whilst maintaining high enantioselectivity in a model reaction.

  一个新的褶皱：构象明确的硫脲催化剂，如图所示，通过分子内氢键稳定，表现出配体-受体的协同作用。这种构象导致催化效率显着提高，从而导致更高的周转率和更低的催化剂负载量，同时在模型反应中保持了高对映选择性。
• Enantioselective total synthesis of (+)-arborescidine C and related tetracyclic indole alkaloids using organocatalysis
  作者：Vishal M. Sheth、Bor-Cherng Hong、Gene-Hsiang Lee

  DOI：10.1039/c7ob00473g

  日期：——

  A concise and enantioselective synthesis of the tetracyclic indoles, including the naturally occurring compounds (+)-arborescidine C and (+)-arborescidine B, was achieved by the key step of Pictet–Spengler cyclization reaction with a Jacobsen-type thiourea organocatalyst. The synthetic process was further demonstrated in a pot-economy strategy and was achieved in a one-pot operation.

  通过与雅各布森型硫脲有机催化剂进行Pictet-Spengler环化反应的关键步骤，可以实现包括自然存在的化合物（+）-碳硼烷C和（+）-碳硼烷B在内的四环吲哚的简明和对映选择性合成。合成工艺在锅经济策略中得到了进一步证明，并在一锅操作中得以实现。
• Enantioselective Thiourea-Catalyzed Acyl-Mannich Reactions of Isoquinolines
  作者：Mark S. Taylor、Norihito Tokunaga、Eric N. Jacobsen

  DOI：10.1002/anie.200502277

  日期：2005.10.21
• Highly Enantioselective Catalytic Acyl-Pictet−Spengler Reactions
  作者：Mark S. Taylor、Eric N. Jacobsen

  DOI：10.1021/ja046259p

  日期：2004.9.1

  The enantioselective cyclization of N-acyliminium ions generated in situ from tryptamine is promoted with high enantioselectivity by a new chiral thiourea catalyst. This represents the first successful system for asymmetric catalysis of the Pictet-Spengler reaction.