(S)-2-((1S,3R)-3-tert-Butoxycarbonylamino-1-methyl-butyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester | 198976-16-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-2-((1S,3R)-3-tert-Butoxycarbonylamino-1-methyl-butyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
• 英文别名: methyl (4S)-2-[(2S,4R)-4-[(2-methylpropan-2-yl)oxycarbonylamino]pentan-2-yl]-4,5-dihydro-1,3-oxazole-4-carboxylate
• CAS: 198976-16-8
• 化学式: C₁₅H₂₆N₂O₅
• 分子量: 314.382
• InChiKey: HGWUALIAKDCWQD-AXFHLTTASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  22
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  86.2
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (S)-2-((1S,3R)-3-tert-Butoxycarbonylamino-1-methyl-butyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 在 双(三甲基硅烷基)氨基钾 、 lithium hexamethyldisilazane 作用下， 生成 2-((1S,3R)-3-tert-Butoxycarbonylamino-1-methyl-butyl)-oxazole-4-carboxylic acid methyl ester
  参考文献：
  名称：

  Formation of Stable Spiro[4.4] Ortho Ester Aminals during the Synthesis of the C₂₆−C₃₂ Oxazole Fragment of Calyculin C

  摘要：

  DOI：

  10.1021/jo981674j
• 作为产物：
  描述：

  (4R)-2-methyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid 在 N-甲基吗啉 、 吡啶 、 氯化亚砜 、 氯甲酸异丁酯 作用下， 反应 0.17h， 生成 (S)-2-((1S,3R)-3-tert-Butoxycarbonylamino-1-methyl-butyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester
  参考文献：
  名称：

  Synthesis of the C₂₆−C₃₂ Oxazole Fragment of Calyculin C:  A Test Case for Oxazole Syntheses

  摘要：

  The synthesis of the C-26-C-32 oxazole fragment 4 and its C-32 epimer 20 of serine/threonine protein phosphatase PP1 and PP2A inhibitor calyculin C is presented. The syn methyl arrangement in 4 was established through cyclic stereocontrol. Several methods for oxidizing the intermediate oxazolines 18 and 19 to the finished oxazole fragments were explored. The best results were obtained with oxidations proceeding through the corresponding ester enolate when the carbamate NH side chain was temporarily protected with a TMS group, or with CuBr2/DBU/HMTA-based oxidations. The finished oxazole fragment 4 was obtained in 21% overall yield, starting from Boc-D-alaninal.

  DOI：

  10.1021/jo971167m

文献信息

• Formation of Stable Spiro[4.4] Ortho Ester Aminals during the Synthesis of the C₂₆−C₃₂ Oxazole Fragment of Calyculin C
  作者：Petri M. Pihko、Ari M. P. Koskinen、Maija J. Nissinen、Kari Rissanen

  DOI：10.1021/jo981674j

  日期：1999.1.1
• Synthesis of the C₂₆−C₃₂ Oxazole Fragment of Calyculin C:  A Test Case for Oxazole Syntheses
  作者：Petri M. Pihko、Ari M. P. Koskinen

  DOI：10.1021/jo971167m

  日期：1998.1.1

  The synthesis of the C-26-C-32 oxazole fragment 4 and its C-32 epimer 20 of serine/threonine protein phosphatase PP1 and PP2A inhibitor calyculin C is presented. The syn methyl arrangement in 4 was established through cyclic stereocontrol. Several methods for oxidizing the intermediate oxazolines 18 and 19 to the finished oxazole fragments were explored. The best results were obtained with oxidations proceeding through the corresponding ester enolate when the carbamate NH side chain was temporarily protected with a TMS group, or with CuBr2/DBU/HMTA-based oxidations. The finished oxazole fragment 4 was obtained in 21% overall yield, starting from Boc-D-alaninal.