4-methoxyphenyl{(1R)-2,2,2-trifluoro-1-[(4R)-4-phenyl-4,5-dihydro-1,3-oxazol-2-ylmethyl]ethyl}amine | 367491-10-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 4-methoxyphenyl{(1R)-2,2,2-trifluoro-1-[(4R)-4-phenyl-4,5-dihydro-1,3-oxazol-2-ylmethyl]ethyl}amine
• 英文别名: 4-methoxy-N-[(2R)-1,1,1-trifluoro-3-[(4R)-4-phenyl-4,5-dihydro-1,3-oxazol-2-yl]propan-2-yl]aniline
• CAS: 367491-10-9
• 化学式: C₁₉H₁₉F₃N₂O₂
• 分子量: 364.367
• InChiKey: WDYAAKLTZAYVMD-DLBZAZTESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  42.8
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  4-methoxyphenyl{(1R)-2,2,2-trifluoro-1-[(4R)-4-phenyl-4,5-dihydro-1,3-oxazol-2-ylmethyl]ethyl}amine 在 盐酸 作用下， 反应 4.0h， 生成 (R)-isopropyl 4,4,4-trifluoro-3-(4-methoxyphenylamino)butanoate
  参考文献：
  名称：

  Novel strategy for the synthesis of fluorinated β-amino acid derivatives from Δ2-oxazolines

  摘要：

  Racemic and chiral non-racemic beta -fluoroalkyl-beta -amino acid derivatives have been prepared in two steps starting from 2-alkyl-Delta (2)-oxazolines and fluorinated imidoyl chlorides. Subsequent chemoselective reduction of the C-masked beta -enamino acid derivatives initially formed provided the target beta -amino acids. The process takes place with total chemoselectivity, high yields and satisfactory diastereoselectivity. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(01)00539-7
• 作为产物：
  描述：

  (R)-2-methyl-4-phenyl-Δ²-oxazoline 在 zinc(II) iodide 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 4-methoxyphenyl{(1R)-2,2,2-trifluoro-1-[(4R)-4-phenyl-4,5-dihydro-1,3-oxazol-2-ylmethyl]ethyl}amine
  参考文献：
  名称：

  Novel strategy for the synthesis of fluorinated β-amino acid derivatives from Δ2-oxazolines

  摘要：

  Racemic and chiral non-racemic beta -fluoroalkyl-beta -amino acid derivatives have been prepared in two steps starting from 2-alkyl-Delta (2)-oxazolines and fluorinated imidoyl chlorides. Subsequent chemoselective reduction of the C-masked beta -enamino acid derivatives initially formed provided the target beta -amino acids. The process takes place with total chemoselectivity, high yields and satisfactory diastereoselectivity. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(01)00539-7

文献信息

• New Strategy for the Stereoselective Synthesis of Fluorinated β-Amino Acids
  作者：Santos Fustero、Belén Pina、Esther Salavert、Antonio Navarro、M. Carmen Ramírez de Arellano、Antonio Simón Fuentes

  DOI：10.1021/jo025621k

  日期：2002.7.1

  Racemic and chiral nonracemic alpha-substituted and alpha-unsubstituted beta-fluoroalkyl beta-amino acid derivatives 6 and 9 have been synthesized in two steps starting from fluorinated imidoyl chlorides 1 and ester enolates. This approach is based on the chemical reduction of previously obtained gamma-fluorinated beta-enamino esters 4 by using ZnI2/NaBH4 in a nonchelated aprotic medium (dry CH2Cl2) as the reducing agent. A metal-chelated six-membered model has been suggested to explain the stereochemical outcome of the reduction reaction. The process takes place with high yields and with moderate to good diastereoselectivity. The best results related to diastereoselective reduction of chiral beta-enamino esters 4 were provided by the use of (-)-8-phenylmenthol as a chiral auxiliary.