3-cyano-4-methyl-1-naphthoyl chloride | 465536-30-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 3-cyano-4-methyl-1-naphthoyl chloride
• 英文别名: 3-Cyano-4-methyl-1-naphthoyl chloride；3-cyano-4-methylnaphthalene-1-carbonyl chloride
• CAS: 465536-30-5
• 化学式: C₁₃H₈ClNO
• 分子量: 229.666
• InChiKey: MFQRPFQIOYEHNV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  40.9
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-cyano-4-methyl-1-naphthoyl chloride 、 N-[(S)-2-(3,4-dichlorophenyl)-4-[4-[(S)-2-methylsulfinylphenyl]-1-piperidinyl]butyl]-N-methylamine 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 以84%的产率得到N-[2-(S)-(3,4-dichlorophenyl)-4-[4-[(S)-2-methylsulfinylphenyl]-1-piperidinyl]butyl]-N-methyl-3-cyano-6-methyl-1-naphthamide
  参考文献：
  名称：

  Design, Synthesis, and SAR of Tachykinin Antagonists:  Modulation of Balance in NK₁/NK₂ Receptor Antagonist Activity

  摘要：

  Through optimization of compounds based on the dual NK1/NK2 antagonist ZD6021, it was found that alteration of two key regions could modulate the balance of NK1 and NK2 potency. Substitution of the 2-naphthalene position in analogues of ZD6021 resulted in increased NK1 potency and thus afforded NK1 preferential antagonists. Alterations of the piperidine region could then increase NK2 potency to restore dual NK1/NK2 selectivity. Through these efforts, three novel receptor antagonists from a single chemically related series were identified; two are dual NK1/NK2 antagonists, and the third is an NK1 preferential antagonist. In this paper, the factors affecting the balance of NK1 and NK2 selectivity in this series are discussed and the in vitro and in vivo properties of the novel antagonists are described.

  DOI：

  10.1021/jm020094i
• 作为产物：
  描述：

  3-hydroxy-4-methyl-1-naphthoic acid 在 四(三苯基膦)钯 lithium hydroxide 、 草酰氯 、 碳酸氢钠 、 三乙胺 、 N,N-二甲基甲酰胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 丙酮 为溶剂， 反应 26.0h， 生成 3-cyano-4-methyl-1-naphthoyl chloride
  参考文献：
  名称：

  Design, Synthesis, and SAR of Tachykinin Antagonists:  Modulation of Balance in NK₁/NK₂ Receptor Antagonist Activity

  摘要：

  Through optimization of compounds based on the dual NK1/NK2 antagonist ZD6021, it was found that alteration of two key regions could modulate the balance of NK1 and NK2 potency. Substitution of the 2-naphthalene position in analogues of ZD6021 resulted in increased NK1 potency and thus afforded NK1 preferential antagonists. Alterations of the piperidine region could then increase NK2 potency to restore dual NK1/NK2 selectivity. Through these efforts, three novel receptor antagonists from a single chemically related series were identified; two are dual NK1/NK2 antagonists, and the third is an NK1 preferential antagonist. In this paper, the factors affecting the balance of NK1 and NK2 selectivity in this series are discussed and the in vitro and in vivo properties of the novel antagonists are described.

  DOI：

  10.1021/jm020094i

文献信息

• [EN] NAPHTHAMIDE DERIVATIVES AND THEIR USE<br/>[FR] DERIVES DE NAPHTAMIDE ET LEUR UTILISATION
  申请人：ASTRAZENECA AB

  公开号：WO2004020411A1

  公开（公告）日：2004-03-11

  Compounds having the following structure wherein R1, R2, R3, R4, m and n are as defined in the specification, in vivo-hydrolysable precursors thereof, pharmaceutically-acceptable salts thereof, the use in therapy and pharmaceutical compositions and methods of treatment using the same.

  具有以下结构的化合物，其中R1、R2、R3、R4、m和n如规范中定义，其体内可水解的前体，其药用可接受的盐，以及在治疗中的使用、制药组合物和使用相同方法的治疗方法。
• Naphthamide derivatives and their use
  申请人：Bernstein Peter

  公开号：US20060241142A1

  公开（公告）日：2006-10-26

  Compounds having the following structure wherein R 1 , R 2 , R 3 , R 4 , m and n are as defined in the specification, in vivo-hydrolysable precursors thereof, pharmaceutically-acceptable salts thereof, the use in therapy and pharmaceutical compositions and methods of treatment using the same.

  具有以下结构的化合物，其中R1、R2、R3、R4、m和n如规范中所定义，其体内可水解的前体，其药学上可接受的盐，以及在治疗中的使用和制药组合物和使用它们的治疗方法。
• NAPHTHAMIDE DERIVATIVES AND THEIR USE
  申请人：AstraZeneca AB

  公开号：EP1549615A1

  公开（公告）日：2005-07-06