(+)-(4S)-3-(Benzyloxycarbonyl)-4-<3-(ethoxycarbonyl)-2-oxo-3-(triphenylphosphoranylidene)propyl>-1,3-oxazolidin-5-one | 167280-62-8

• 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: (+)-(4S)-3-(Benzyloxycarbonyl)-4-<3-(ethoxycarbonyl)-2-oxo-3-(triphenylphosphoranylidene)propyl>-1,3-oxazolidin-5-one
• 英文别名: benzyl (4S)-4-[4-ethoxy-2,4-dioxo-3-(triphenyl-lambda5-phosphanylidene)butyl]-5-oxo-1,3-oxazolidine-3-carboxylate；benzyl (4S)-4-[4-ethoxy-2,4-dioxo-3-(triphenyl-λ5-phosphanylidene)butyl]-5-oxo-1,3-oxazolidine-3-carboxylate
• CAS: 167280-62-8
• 化学式: C₃₅H₃₂NO₇P
• 分子量: 609.615
• InChiKey: KQLCIOPFPUTPRG-PMERELPUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  44
• 可旋转键数：
  12
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  99.2
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  (+)-(4S)-3-(Benzyloxycarbonyl)-4-<3-(ethoxycarbonyl)-2-oxo-3-(triphenylphosphoranylidene)propyl>-1,3-oxazolidin-5-one 在 sodium hydroxide 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 68.0h， 生成 (+)-(5S)-Ethyl 5-<(benzyloxycarbonyl)amino>-5-carbamoyl>-3-oxopentanoate
  参考文献：
  名称：

  Synthesis of Cyclic Acylated Enamino Esters from Enol Lactones, 4-Keto amides, and 5-Hydroxy Lactams

  摘要：

  Enol lactones react with an amine to give either a keto amide or a hydroxy lactam under mild conditions. Subsequent dehydration with p-toluenesulfonic acid (PTSA) gives a cyclic acylated enamino ester in good yield (Tables 1 and 2, Schemes 2 and 4). The key prostaglandin analog precursor 18 and the gly-gly dipeptide analogs 26a and 26b were prepared using the reported conditions. Acetylation of the chloro hydroxy lactam 31, prepared from the chloro enol lactones 29, followed by elimination of acetic acid gave the chloro acylated enamino esters 28.

  DOI：

  10.1021/jo00110a026
• 作为产物：
  描述：

  (S)-(+)-3(苄氧羰基)-5-氧代-4-恶唑啉乙酸 在 草酰氯 、 N,N-二甲基甲酰胺 作用下， 以 二氯甲烷 为溶剂， 反应 19.0h， 生成 (+)-(4S)-3-(Benzyloxycarbonyl)-4-<3-(ethoxycarbonyl)-2-oxo-3-(triphenylphosphoranylidene)propyl>-1,3-oxazolidin-5-one
  参考文献：
  名称：

  Synthesis of Cyclic Acylated Enamino Esters from Enol Lactones, 4-Keto amides, and 5-Hydroxy Lactams

  摘要：

  Enol lactones react with an amine to give either a keto amide or a hydroxy lactam under mild conditions. Subsequent dehydration with p-toluenesulfonic acid (PTSA) gives a cyclic acylated enamino ester in good yield (Tables 1 and 2, Schemes 2 and 4). The key prostaglandin analog precursor 18 and the gly-gly dipeptide analogs 26a and 26b were prepared using the reported conditions. Acetylation of the chloro hydroxy lactam 31, prepared from the chloro enol lactones 29, followed by elimination of acetic acid gave the chloro acylated enamino esters 28.

  DOI：

  10.1021/jo00110a026

文献信息

• Synthesis of Cyclic Acylated Enamino Esters from Enol Lactones, 4-Keto amides, and 5-Hydroxy Lactams
  作者：A. D. Abell、M. D. Oldham、J. M. Taylor

  DOI：10.1021/jo00110a026

  日期：1995.3

  Enol lactones react with an amine to give either a keto amide or a hydroxy lactam under mild conditions. Subsequent dehydration with p-toluenesulfonic acid (PTSA) gives a cyclic acylated enamino ester in good yield (Tables 1 and 2, Schemes 2 and 4). The key prostaglandin analog precursor 18 and the gly-gly dipeptide analogs 26a and 26b were prepared using the reported conditions. Acetylation of the chloro hydroxy lactam 31, prepared from the chloro enol lactones 29, followed by elimination of acetic acid gave the chloro acylated enamino esters 28.