2,2,2-trifluoro-N-(1-oxo-1-phenylpropaN-2-yl)acetamide | 16735-27-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,2,2-trifluoro-N-(1-oxo-1-phenylpropaN-2-yl)acetamide
• 英文别名: N-(trifluoroacetyl)-α-amino-propiophenone；(RS)-2-trifluoroacetamido-1-phenyl-1-propanone；α-Trifluoracetamido-propiophenon；2-Trifluoroacetamido-propiophenon
• CAS: 16735-27-6
• 化学式: C₁₁H₁₀F₃NO₂
• 分子量: 245.201
• InChiKey: UEYXKCJEHHETCG-UHFFFAOYSA-N

物化性质

• 熔点：
  74-76 °C
• 沸点：
  340.2±42.0 °C(Predicted)
• 密度：
  1.269±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  46.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2,2,2-trifluoro-N-(1-oxo-1-phenylpropaN-2-yl)acetamide 在 aluminum isopropoxide 作用下， 生成 rac-(1R,2S)-N-(2-hydroxy-1-methyl-2-phenylethyl)-2,2,2-trifluoroacetamide
  参考文献：
  名称：

  Mueller,H.K. et al., Journal fur praktische Chemie (Leipzig 1954), 1973, vol. 315, p. 1045 - 1056

  摘要：

  DOI：
• 作为产物：
  描述：

  trifluoroacetyl-DL-alanine 在 三氯化铝 、 草酸氯化物 作用下， 以 吡啶 、 苯 为溶剂， 反应 3.25h， 生成 2,2,2-trifluoro-N-(1-oxo-1-phenylpropaN-2-yl)acetamide
  参考文献：
  名称：

  Friedel-Crafts acylation with N-(trifluoroacetyl)-.alpha.-amino acid chlorides. Application to the preparation of .beta.-arylalkylamines and 3-substituted 1,2,3,4-tetrahydroisoquinolines

  摘要：

  DOI：

  10.1021/jo00196a001

文献信息

• Photoactivated <i>N</i> ‐Acyliminoiodinanes Applied to Amination: an <i>ortho</i> ‐Methoxymethyl Group Stabilizes Reactive Precursors
  作者：Yusuke Kobayashi、Sota Masakado、Yoshiji Takemoto

  DOI：10.1002/anie.201710277

  日期：2018.1.15

  the first time by X‐ray structural analysis. The ortho‐methoxymethyl group and the carbonyl oxygen coordinate to the iodine atom of the iminoiodinane. Activation of the N‐acyliminoiodinane was achieved by photoirradiation at 370 nm, thereby enabling reaction with various silyl enol ethers to give α‐aminoketone derivatives in good to high yield. N‐sulfonyliminoiodinanes bearing ortho substituents were

  X射线结构分析首次表征了N-环戊碘烷。的邻-甲氧基和羰基氧坐标到iminoiodinane的碘原子。通过在370 nm处进行光辐照可以实现N-酰基亚氨基碘的活化，从而使其能够与各种甲硅烷基烯醇醚反应，从而以高至高收率得到α-氨基酮衍生物。带有邻位取代基的N-磺酰亚胺基碘烷在光诱导的胺化反应中被使用。
• MAO inhibition by arylisopropylamines: the effect of oxygen substituents at the β-position
  作者：Mauricio Osorio-Olivares、Marcos Caroli Rezende、Silvia Sepúlveda-Boza、Bruce K Cassels、Angélica Fierro

  DOI：10.1016/j.bmc.2004.05.033

  日期：2004.8.1

  Twenty-nine arylisopropylamines, substituted at the beta-position of their side chain by an oxo, hydroxy, or methoxy group, were evaluated in vitro as MAO-A and MAO-B inhibitors. The oxo derivatives ('cathinones') were in general less active as MAO-A inhibitors than the corresponding arylisopropylamines, but exhibited an interesting MAO-13 inhibiting activity, which was absent in the hydroxy, methoxy, and beta-unsubstituted analogues. These results suggest that selective affinity for the two MAO isoforms in this family of compounds is modulated not only by the aryl substitution pattern but also by the side-chain substituents on the aryl-alkylamine scaffold. (C) 2004 Elsevier Ltd. All rights reserved.
• 5-Aryl-imidazolin-2-ones as a scaffold for potent antioxidant and memory-improving activity
  作者：Kazutoshi Watanabe、Yasuhiro Morinaka、Yoshio Hayashi、Masaki Shinoda、Hiroyoshi Nishi、Nobuko Fukushima、Toshiaki Watanabe、Akira Ishibashi、Satoshi Yuki、Masahiko Tanaka

  DOI：10.1016/j.bmcl.2007.12.064

  日期：2008.2

  A series of 5-phenyl-substituted-N-alkyl-imidazolin-2-ones with potent radical-scavenging activity and lipid peroxidation inhibitory activity was synthesized. Many of the compounds showed memory-improving effect in animal models independent of the inhibitory activity on lipid peroxidation. (c) 2008 Elsevier Ltd. All rights reserved.
• NORDLANDER, J. E.;PAYNE, M. J.;NJOROGE, F. G.;BALK, M. A.;LAIKOS, G. D.;V+, J. ORG. CHEM., 1984, 49, N 22, 4107-4111
  作者：NORDLANDER, J. E.、PAYNE, M. J.、NJOROGE, F. G.、BALK, M. A.、LAIKOS, G. D.、V+

  DOI：——

  日期：——
• Friedel-Crafts acylation with N-(trifluoroacetyl)-.alpha.-amino acid chlorides. Application to the preparation of .beta.-arylalkylamines and 3-substituted 1,2,3,4-tetrahydroisoquinolines
  作者：J. Eric Nordlander、Mark J. Payne、F. George Njoroge、Michael A. Balk、George D. Laikos、Vasanth M. Vishwanath

  DOI：10.1021/jo00196a001

  日期：1984.11

表征谱图