N-(5,7-dimethyl-2-oxo-2H,3H-[1,3]thiazolo[4,5-b]pyridin-6-yl)acetamide

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N-(5,7-dimethyl-2-oxo-2H,3H-[1,3]thiazolo[4,5-b]pyridin-6-yl)acetamide
• 英文别名: N-(5,7-dimethyl-2-oxo-3H-[1,3]thiazolo[4,5-b]pyridin-6-yl)acetamide
• 化学式: C₁₀H₁₁N₃O₂S
• 分子量: 237.282
• InChiKey: BOIHOLKQZRLCHG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  96.4
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  pentane-2,3,4-trione 3-phenylhydrazone 在 吡啶 、 sodium 、 溶剂黄146 、 三乙胺 、 锌 作用下， 以 1,4-二氧六环 、 甲醇 为溶剂， 反应 169.25h， 生成 N-(5,7-dimethyl-2-oxo-2H,3H-[1,3]thiazolo[4,5-b]pyridin-6-yl)acetamide
  参考文献：
  名称：

  Synthesis and Antioxidant Activity Evaluation of Novel 5,7-dimethyl-3H-Thiazolo[4,5-B]Pyridines

  摘要：

  5,7-Dimethyl-3H-thiazolo[4,5-b]pyridine-2-one was obtained under the reaction of 4-iminothiazolidin-2-one with acetylacetone. Further structural modifications include the introduction of diversity at the N-3 and C-6 positions. The antioxidant activity of the synthesized compounds was evaluated in vitro by the method of scavenging effect on 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals. [Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the following free supplemental files: Additional figures]

  DOI：

  10.1080/10426507.2013.777723