(3RS,4S)-4-N-(tert-butyloxycarbonyl)amino-3-hydroxy-2-methyl-5-phenylpent-1-ene | 265996-13-2

• 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: (3RS,4S)-4-N-(tert-butyloxycarbonyl)amino-3-hydroxy-2-methyl-5-phenylpent-1-ene
• 英文别名: (4S)-4-tert-butoxycarbonylamino-2-methyl-5-phenylpent-1-en-3-ol；tert-butyl N-[(2S)-3-hydroxy-4-methyl-1-phenylpent-4-en-2-yl]carbamate
• CAS: 265996-13-2
• 化学式: C₁₇H₂₅NO₃
• 分子量: 291.39
• InChiKey: PXDPNAWEFXOQNZ-MLCCFXAWSA-N

物化性质

• 沸点：
  438.8±45.0 °C(Predicted)
• 密度：
  1.054±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  21
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (3RS,4S)-4-N-(tert-butyloxycarbonyl)amino-3-hydroxy-2-methyl-5-phenylpent-1-ene 在 1-羟基苯并三唑 、 戴斯-马丁氧化剂 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 间氯过氧苯甲酸 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 16.5h， 生成 N-{(2S)-4-methyl-1-{3-[(2S)-1-((2R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-ylamino]-3-oxo-1-phenylpropylamino}-1-oxopentan-2-yl}benzamide
  参考文献：
  名称：

  Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors

  摘要：

  A series of novel tripeptidyl epoxyketone derivatives constructed from beta-amino acid were designed, synthesized and evaluated as proteasome inhibitors. All target compounds were tested for their proteasome inhibitory activities and selected compounds were tested for their anti-proliferation activities against two multiple myeloma (MM) cell lines RPMI 8226 and NCI-H929. Among them, eleven compounds exhibited proteasome inhibitory rates of more than 50% at the concentration of 1 mu g/mL and nine compounds showed anti-proliferation activities with IC50 values at low micromolar level. Compound 20h displayed the most potent proteasome inhibitory activities (IC50: 0.11 +/- 0.01 mu M) and anti-proliferation activities with IC50 values at 0.23 +/- 0.01 and 0.17 +/- 0.02 mu M against two tested cell lines. Additionally, the poly-ubiquitin accumulation in the western blot analysis supported that proteasome inhibition in a cellular system was induced by compound 20h. All these experimental results confirmed that b-amino acid can be introduced as a building block for the development of proteasome inhibitors. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2014.04.011
• 作为产物：
  描述：

  BOC-PHE-甲氧基甲胺 在 sodium tetrahydroborate 、 cerium(III) chloride heptahydrate 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 2.0h， 生成 (3RS,4S)-4-N-(tert-butyloxycarbonyl)amino-3-hydroxy-2-methyl-5-phenylpent-1-ene
  参考文献：
  名称：

  Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors

  摘要：

  A series of novel tripeptidyl epoxyketone derivatives constructed from beta-amino acid were designed, synthesized and evaluated as proteasome inhibitors. All target compounds were tested for their proteasome inhibitory activities and selected compounds were tested for their anti-proliferation activities against two multiple myeloma (MM) cell lines RPMI 8226 and NCI-H929. Among them, eleven compounds exhibited proteasome inhibitory rates of more than 50% at the concentration of 1 mu g/mL and nine compounds showed anti-proliferation activities with IC50 values at low micromolar level. Compound 20h displayed the most potent proteasome inhibitory activities (IC50: 0.11 +/- 0.01 mu M) and anti-proliferation activities with IC50 values at 0.23 +/- 0.01 and 0.17 +/- 0.02 mu M against two tested cell lines. Additionally, the poly-ubiquitin accumulation in the western blot analysis supported that proteasome inhibition in a cellular system was induced by compound 20h. All these experimental results confirmed that b-amino acid can be introduced as a building block for the development of proteasome inhibitors. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2014.04.011

文献信息

• Enantioselective Synthesis of 3,6-Dihydro-1<i>H</i>-pyridin-2-ones:  Unexpected Regioselectivity in the Palladium-Catalyzed Decarboxylative Carbonylation of 5-Vinyloxazolidin-2-ones
  作者：Julian G. Knight、Simon W. Ainge、Andrew M. Harm、Simon J. Harwood、Haydn I. Maughan、Duncan R. Armour、David M. Hollinshead、Albert A. Jaxa-Chamiec

  DOI：10.1021/ja993897c

  日期：2000.3.1
• Stereoselective Synthesis of MeBmt and Methyl (4<i>R</i>,5<i>S</i>)-5-Isopropyl-2- phenyloxazoline-4-carboxylate by a Pd-Catalyzed Equilibration
  作者：Gregory R. Cook、P. Sathya Shanker

  DOI：10.1021/jo015760m

  日期：2001.10.1