_{6-chloro-9-(oxiran-2-ylmethyl)-9H-purine} | 241823-43-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: _{6-chloro-9-(oxiran-2-ylmethyl)-9H-purine}
• 英文别名: 9-(2,3-epoxypropyl)-6-chloro-9H-purine；6-Chloro-9-(oxiran-2-ylmethyl)purine
• CAS: 241823-43-8
• 化学式: C₈H₇ClN₄O
• 分子量: 210.623
• InChiKey: WKPFQWWVBKPDJS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  56.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  _{6-chloro-9-(oxiran-2-ylmethyl)-9H-purine} 在 β-环糊精 、 硫脲 作用下， 以 水 、 丙酮 为溶剂， 反应 4.17h， 以96%的产率得到6-chloro-9-(thiiran-2-ylmethyl)-9H-purine
  参考文献：
  名称：

  Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity

  摘要：

  An efficient and mild method has been developed for the preparation of 9-oxiranyl-9H-purine derivatives. This reaction proceeds smoothly in beta-cyclodextrin cavity at room temperature, giving good to excellent yields. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.12.117
• 作为产物：
  描述：

  9-allyl-6-chloro-9H-purine 在 β-环糊精 、 Oxone 、 碳酸氢钠 作用下， 以 水 、 丙酮 为溶剂， 反应 6.17h， 以90%的产率得到_{6-chloro-9-(oxiran-2-ylmethyl)-9H-purine}
  参考文献：
  名称：

  Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity

  摘要：

  An efficient and mild method has been developed for the preparation of 9-oxiranyl-9H-purine derivatives. This reaction proceeds smoothly in beta-cyclodextrin cavity at room temperature, giving good to excellent yields. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.12.117

文献信息

• Synthesis and biological evaluation of the novel purine and pyrimidine nucleoside analogues containing 2,3-epoxypropyl, 3-amino-2-hydroxypropyl or 2,3-epoxypropyl ether moieties
  作者：Silvana Raić-Malić、Mira Grdiša、Krešimir Pavelic、Mladen Mintas

  DOI：10.1016/s0223-5234(99)80090-7

  日期：1999.5

  The novel purine and pyrimidine nucleoside analogues possessing a 2,3-epoxypropyl (2a-2c and 8a-8c), 2,3-epoxypropyl ether (3), or 3-amino-2-hydroxypropyl (4a-6c and 9a-9c) moiety bonded at either N-9 of the C-6 substituted purine ring or N-1 and N-3 of the pyrimidine ring, were prepared and evaluated on their antitumour and antiviral activities. Compounds 3, 6b, 8b and sc showed marked inhibition of growth of human tumour cell lines (MiaPaCa(2) and Raji), whilst the inhibitory effect of 6b was greater against Raji cells than to the MiaPaCa2 ones. No specific activity of compounds 2a-3, 4a-6c and 9a-9c against HSV and VZV was detected. The compound 6b was slightly active against the replication of HIV 1 (IIIB), while 2a-2c and 8a-8c were inactive. (C) Elsevier, Paris.
• Synthesis of 9-oxiranyl-9H-purine derivatives in β-cyclodextrin cavity
  作者：Qian Zhang、Yong-Zhen Huang、Jun-Hui Yang、Bai-Wei Ma、Gui-Rong Qu、Hai-Ming Guo

  DOI：10.1016/j.tetlet.2013.12.117

  日期：2014.2

  An efficient and mild method has been developed for the preparation of 9-oxiranyl-9H-purine derivatives. This reaction proceeds smoothly in beta-cyclodextrin cavity at room temperature, giving good to excellent yields. (C) 2014 Elsevier Ltd. All rights reserved.