quinoline-8-sulfonyl chloride

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: quinoline-8-sulfonyl chloride
• 英文别名: Quinolin-8-ylsulfonylformyl chloride
• 化学式: C₁₀H₆ClNO₃S
• 分子量: 255.682
• InChiKey: ULVBMJGRNHEYOK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  72.5
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  5-氨基-1,3-二苯基哌唑 、 quinoline-8-sulfonyl chloride 以 二氯甲烷 为溶剂， 以90%的产率得到N-(2,5-diphenylpyrazol-3-yl)-1-quinolin-8-ylsulfonylformamide
  参考文献：
  名称：

  An efficient one-pot synthesis of N-(1,3-diphenyl-1H-pyrazol- 5-yl)amides

  摘要：

  Abstractmagnified image A “one‐pot” method for the synthesis of N‐(1,3‐diphenyl‐1H‐pyrazol‐5‐yl)amides was developed by cyclization of benzoylacetonitrile (1) and phenylhydrazine in neat condition followed by acylation. The corresponding N‐(1,3‐diphenyl‐1H‐pyrazol‐5‐yl)amides were provided in good to excellent yields (70–90%). The significant advantages of the new synthetic method are excellent yields and simple work‐up procedure without isolation and purification of intermediary 5‐amino‐1,3‐diphenyl pyrazol (2). J. Heterocyclic Chem., (2010).

  DOI：

  10.1002/jhet.343

文献信息

• An efficient one-pot synthesis of N-(1,3-diphenyl-1H-pyrazol- 5-yl)amides
  作者：Wei-Nien Su、Tsung-Ping Lin、Kaung-Min Cheng、Kuan-Chin Sung、Shao-Kai Lin、Fung Fuh Wong

  DOI：10.1002/jhet.343

  日期：——

  Abstractmagnified image A “one‐pot” method for the synthesis of N‐(1,3‐diphenyl‐1H‐pyrazol‐5‐yl)amides was developed by cyclization of benzoylacetonitrile (1) and phenylhydrazine in neat condition followed by acylation. The corresponding N‐(1,3‐diphenyl‐1H‐pyrazol‐5‐yl)amides were provided in good to excellent yields (70–90%). The significant advantages of the new synthetic method are excellent yields and simple work‐up procedure without isolation and purification of intermediary 5‐amino‐1,3‐diphenyl pyrazol (2). J. Heterocyclic Chem., (2010).