2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one | 914360-74-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one
• CAS: 914360-74-0
• 化学式: C₁₄H₁₃ClN₂O
• 分子量: 260.723
• InChiKey: DSKKLLICJQWECG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  42.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one 在 氨 、 对甲苯磺酸 作用下， 以 甲醇 、 xylene 为溶剂， 反应 72.0h， 以75%的产率得到7-ethyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine
  参考文献：
  名称：

  Highly selective substitutions in 2,3-dichloropyrazine. A novel general approach to aloisines

  摘要：

  A highly efficient synthesis of the potent CDKs (cyclin-dependent kinases) inhibitors, aloisines (substituted 5H-pyrrolo[2,3b]pyrazines) is presented. The method is based on highly selective monosubstitution of a single chlorine atom in 2,3-dichloropyrazine with lithiated ketones, esters, and nitriles followed by co-cyclization of the resulting intermediates with primary amines or hydrazines. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.08.018
• 作为产物：
  描述：

  2,3-二氯吡嗪 、 苯丁酮 在 lithium hexamethyldisilazane 作用下， 以 甲苯 为溶剂， 反应 24.0h， 以96%的产率得到2-(3-chloropyrazin-2-yl)-1-phenylbutan-1-one
  参考文献：
  名称：

  Highly selective substitutions in 2,3-dichloropyrazine. A novel general approach to aloisines

  摘要：

  A highly efficient synthesis of the potent CDKs (cyclin-dependent kinases) inhibitors, aloisines (substituted 5H-pyrrolo[2,3b]pyrazines) is presented. The method is based on highly selective monosubstitution of a single chlorine atom in 2,3-dichloropyrazine with lithiated ketones, esters, and nitriles followed by co-cyclization of the resulting intermediates with primary amines or hydrazines. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2006.08.018

文献信息

• Highly selective substitutions in 2,3-dichloropyrazine. A novel general approach to aloisines
  作者：Dmitriy S. Chekmarev、Sergey V. Shorshnev、Alexander E. Stepanov、Alexander N. Kasatkin

  DOI：10.1016/j.tet.2006.08.018

  日期：2006.10

  A highly efficient synthesis of the potent CDKs (cyclin-dependent kinases) inhibitors, aloisines (substituted 5H-pyrrolo[2,3b]pyrazines) is presented. The method is based on highly selective monosubstitution of a single chlorine atom in 2,3-dichloropyrazine with lithiated ketones, esters, and nitriles followed by co-cyclization of the resulting intermediates with primary amines or hydrazines. (c) 2006 Elsevier Ltd. All rights reserved.