(S)-N-(1-(3-bromophenyl)ethyl)acetamide | 177750-52-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (S)-N-(1-(3-bromophenyl)ethyl)acetamide
• 英文别名: (S)-N-[1-(3-Bromophenyl)ethyl]Acetamide；N-[(1S)-1-(3-bromophenyl)ethyl]acetamide
• CAS: 177750-52-6
• 化学式: C₁₀H₁₂BrNO
• 分子量: 242.115
• InChiKey: GHEDNSLOXLEUKX-ZETCQYMHSA-N

物化性质

• 沸点：
  385.9±25.0 °C(Predicted)
• 密度：
  1.359±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (S)-N-(1-(3-bromophenyl)ethyl)acetamide 在 硼酸三异丙酯 、 甲基锂 、 叔丁基锂 作用下， 以 四氢呋喃 为溶剂， 生成 (S)-3-(1-acetamidoethyl)phenylboronic acid
  参考文献：
  名称：

  基于咪唑并[4,5-d]噻唑并[5,4-b]吡啶的 IKK2 抑制剂：类风湿性关节炎临床前模型中的合成、SAR、PK/PD 和活性

  摘要：

  描述了基于噻唑的 IKK2 三环抑制剂的合成、构效关系 (SAR) 和生物学评价。化合物被确定在类风湿性关节炎的小鼠模型中有效。

  DOI：

  10.1016/j.bmcl.2010.10.133
• 作为产物：
  描述：

  (S)-N-(1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)acetamide 在 N-溴代丁二酰亚胺(NBS) 、 copper(I) bromide 作用下， 以 乙腈 为溶剂， 反应 12.0h， 生成 (S)-N-(1-(3-bromophenyl)ethyl)acetamide
  参考文献：
  名称：

  Chemoenzymatic synthesis of boron-containing chiral amines and amides

  摘要：

  The first application of lipases as catalysts to obtain optically active boron-containing amines and amides is described. We studied several reaction conditions to achieve the kinetic resolution of boron-containing amines via enantioselective acylation mediated by Candida antarctica lipase B (CAL-B). Excellent enantioselectivity (E>200) and high enantiomeric excess (up to >99%) of both the remaining amines and amides were obtained. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2010.09.011

文献信息

• Modular Monodentate Phosphoramidite Ligands for Rhodium-Catalyzed Enantioselective Hydrogenation
  作者：Yan Liu、Kuiling Ding

  DOI：10.1021/ja052749l

  日期：2005.8.1

  A new class of monodentate phosphoramidite ligands (DpenPhos) has been developed on the basis of the modular concept for Rh(I)-catalyzed asymmetric hydrogenations of a variety of olefin derivatives, affording the corresponding optically active compounds in excellent yields and enantioselectivities. The ligands have the advantages of facile preparation, tunable structure, and broad scope of substrates

  基于 Rh(I) 催化的各种烯烃衍生物的不对称氢化的模块化概念，开发了一类新的单齿亚磷酰胺配体 (DpenPhos)，以优异的产率和对映选择性提供相应的光学活性化合物。这些配体在其 Rh(I) 络合物催化的不对称氢化中具有制备容易、结构可调和底物范围广等优点。
• Transaminases Applied to the Synthesis of High Added-Value Enantiopure Amines
  作者：Caroline E. Paul、María Rodríguez-Mata、Eduardo Busto、Iván Lavandera、Vicente Gotor-Fernández、Vicente Gotor、Susana García-Cerrada、Javier Mendiola、Óscar de Frutos、Iván Collado

  DOI：10.1021/op4003104

  日期：2014.6.20

  stereoselective amination of (hetero)aromatic ketones using transaminases have been studied, such as temperature, pH, substrate concentration, cosolvent, and source and percentage of amino donor, to further optimize the production of enantiopure amines using both (S)- and (R)-selective biocatalysts from commercial suppliers. Interesting enantiopure amino building blocks have been obtained, overcoming some limitations

  研究了使用转氨酶影响（杂）芳族酮的立体选择性胺化的关键参数，例如温度，pH，底物浓度，助溶剂以及氨基供体的来源和百分比，以进一步优化同时使用这两种方法生产对映体纯胺的方法（S） -和（R）选择性生物催化剂来自商业供应商。已经获得了有趣的对映纯氨基结构单元，克服了传统化学合成方法的某些局限性。扩大代表性方法的规模，提供对映体纯形式的卤代和杂芳族胺，分离产率高。
• Rhodium-Catalyzed Enantioselective Hydrogenation of Oxime Acetates
  作者：Kexuan Huang、Shengkun Li、Mingxin Chang、Xumu Zhang

  DOI：10.1021/ol303282u

  日期：2013.2.1

  Rh-catalyzed enantioselective hydrogenation of oxime acetates was first reported, which afforded a new approach for chiral amine synthesis.

  首次报道了肟肟乙酸酯的Rh催化对映选择性氢化，为手性胺的合成提供了一种新方法。
• Practical by Ligand Design: A New Class of Monodentate Phosphoramidite Ligands for Rhodium-Catalyzed Enantioselective Hydrogenations
  作者：Baoguo Zhao、Zheng Wang、Kuiling Ding

  DOI：10.1002/adsc.200606013

  日期：2006.6

  new class of low-cost and easy-to-prepare monodentate phosphoramidite ligands (CydamPhos) has been developed from readily accessible and cheap trans-1,2-diaminocyclohexane as starting material through a three-step transformation. This type of ligands exhibited excellent enantioseletivities and high activities in rhodium(I)-catalyzed asymmetric hydrogenations of dehydro-α-amino acid methyl esters 9 (ee:

  新型的低成本，易于制备的单齿亚磷酰胺配体（CydamPhos）是通过三步转化，从易于获得且便宜的反式-1,2-二氨基环己烷为原料开发的。这种类型的配体在铑（I）催化的脱氢-α-氨基酸甲酯9（ee：96.2-99.8％）和乙酰胺11（91.8-98.8％）的不对称氢化中表现出优异的对映异构性和高活性。基于催化剂前体的分子结构，合理化配体在催化的对映选择性控制上表现出的显着的取代作用。
• 8H-imidazo[4,5-D]thiazolo[4,5-B]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
  申请人：Das Jagabandhu

  公开号：US20060128741A1

  公开（公告）日：2006-06-15

  The present invention provides for thiazolopyridine-based tricyclic compounds having the formula (I), wherein R 1 , R 2 , R 5 and R 6 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.

  本发明提供了具有以下式子（I）的噻唑吡啶基三环化合物，其中R1、R2、R5和R6如本文所述。本发明还提供了包含此类化合物的药物组合物，以及使用此类化合物治疗炎症和免疫性疾病的方法。