(+)-(4S)-3-ethoxy-4-methyl-1,4-dihydropyrazino[2,1-b]quinazolin-6-one | 870673-94-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: (+)-(4S)-3-ethoxy-4-methyl-1,4-dihydropyrazino[2,1-b]quinazolin-6-one
• CAS: 870673-94-2
• 化学式: C₁₄H₁₅N₃O₂
• 分子量: 257.292
• InChiKey: ZNMZGXQXQPOMQX-VIFPVBQESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.91
• 重原子数：
  19.0
• 可旋转键数：
  1.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  56.48
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  (+)-(4S)-3-ethoxy-4-methyl-1,4-dihydropyrazino[2,1-b]quinazolin-6-one 在 sodium iodide 、 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 17.17h， 生成 (-)-(8S)-1,4-dimethoxy-8-methyl-5H,8H-isoquinolino[2',3'-4,3]pyrazino[2,1-b]quinazoline-7,10-dione
  参考文献：
  名称：

  A new stereocontrolled approach to fused polycyclic compounds containing a diketopiperazine ring

  摘要：

  Representative (1S)- and (4S)-alkyl-1,4-dihydropyrazino[2,1-b]quinazoline-3,6-dione lactim ethers were regio- and diastereoselectively alkylated after metallation to give the corresponding 1,4-trans-isomers with retention of the stereocentres. The results were compared with the previously studied lactams. The (1R,4S)-dialkyl derivatives obtained by C(1)-alkyation with bifunctional reagents were lately cyclized to complex polycyclic compounds through a second N(2)-alkylation promoted by sodium iodide. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.08.034
• 作为产物：
  描述：

  triethyloxonium fluoroborate 、 (4S)-4-methyl-1,2,3,4-tetrahydro-5H-pyrazino[2,1-b]quinazoline-3,6-dione 在 sodium carbonate 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以95%的产率得到(+)-(4S)-3-ethoxy-4-methyl-1,4-dihydropyrazino[2,1-b]quinazolin-6-one
  参考文献：
  名称：

  A new stereocontrolled approach to fused polycyclic compounds containing a diketopiperazine ring

  摘要：

  Representative (1S)- and (4S)-alkyl-1,4-dihydropyrazino[2,1-b]quinazoline-3,6-dione lactim ethers were regio- and diastereoselectively alkylated after metallation to give the corresponding 1,4-trans-isomers with retention of the stereocentres. The results were compared with the previously studied lactams. The (1R,4S)-dialkyl derivatives obtained by C(1)-alkyation with bifunctional reagents were lately cyclized to complex polycyclic compounds through a second N(2)-alkylation promoted by sodium iodide. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.08.034