4-(1-hydroxy-5-(naphthalen-2-ylmethyl)-1H-pyrazol-4-yl)piperidine hydrochloride | 1221274-81-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 4-(1-hydroxy-5-(naphthalen-2-ylmethyl)-1H-pyrazol-4-yl)piperidine hydrochloride
• 英文别名: 4-[1-Hydroxy-5-(naphthalen-2-ylmethyl)pyrazol-4-yl]piperidine;hydrochloride
• CAS: 1221274-81-2
• 化学式: C₁₉H₂₁N₃O*ClH
• 分子量: 343.856
• InChiKey: ULQIHOJOBQUOTQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.75
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  50.1
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  ethyl 4-(1-(benzyloxy)-5-(naphthalen-2-ylmethyl)-1H-pyrazol-4-yl)piperidine-1-carboxylate 在 盐酸 作用下， 以 水 为溶剂， 反应 1.0h， 以47%的产率得到4-(1-hydroxy-5-(naphthalen-2-ylmethyl)-1H-pyrazol-4-yl)piperidine hydrochloride
  参考文献：
  名称：

  Novel 4-(Piperidin-4-yl)-1-hydroxypyrazoles as γ-Aminobutyric Acid_A Receptor Ligands: Synthesis, Pharmacology, and Structure−Activity Relationships

  摘要：

  A series of substituted 1-hydroxypyrazole analogues of the GABA(A) receptor partial agonist 5-(4-piperidyl)-3-isoxazolol (4-PIOL) have been synthesized and pharmacologically characterized. Several of the analogues displayed K-i in the low nanomolar range at the native GABAA receptors and potent antagonism of the alpha(1)beta(2)gamma(2) receptor. It appears that several regions situated in proximity to the core of the orthosteric binding site of the GABA(A) receptor are able to accommodate large hydrophobic substituents.

  DOI：

  10.1021/jm100106r

文献信息

• Novel 4-(Piperidin-4-yl)-1-hydroxypyrazoles as γ-Aminobutyric Acid_A Receptor Ligands: Synthesis, Pharmacology, and Structure−Activity Relationships
  作者：Henriette A. Møller、Tommy Sander、Jesper L. Kristensen、Birgitte Nielsen、Jacob Krall、Marianne L. Bergmann、Bolette Christiansen、Thomas Balle、Anders A. Jensen、Bente Frølund

  DOI：10.1021/jm100106r

  日期：2010.4.22

  A series of substituted 1-hydroxypyrazole analogues of the GABA(A) receptor partial agonist 5-(4-piperidyl)-3-isoxazolol (4-PIOL) have been synthesized and pharmacologically characterized. Several of the analogues displayed K-i in the low nanomolar range at the native GABAA receptors and potent antagonism of the alpha(1)beta(2)gamma(2) receptor. It appears that several regions situated in proximity to the core of the orthosteric binding site of the GABA(A) receptor are able to accommodate large hydrophobic substituents.