N-(2-methyl-2-phenylpropyl)-1,2-benzoxazol-3-amine | 1616343-56-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并异恶唑
• 英文名称: N-(2-methyl-2-phenylpropyl)-1,2-benzoxazol-3-amine
• CAS: 1616343-56-6
• 化学式: C₁₇H₁₈N₂O
• 分子量: 266.343
• InChiKey: GTSKFZRBVBRULH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  38.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-fluoro-N-hydroxybenzenecarboxymidoyl chloride 在 potassium tert-butylate 、 三乙胺 作用下， 以 四氢呋喃 、 1,4-二氧六环 为溶剂， 生成 N-(2-methyl-2-phenylpropyl)-1,2-benzoxazol-3-amine
  参考文献：
  名称：

  Design, synthesis and evaluation of phenethylaminoheterocycles as Kv1.5 inhibitors

  摘要：

  Phenethylaminoheterocycles have been prepared and assayed for inhibition of the K(v)1.5 potassium ion channel as a potential approach to the treatment of atrial fibrillation. A diverse set of heterocycles were identified as potent K(v)1.5 inhibitors and were advanced to pharmacodynamic evaluation based on selectivity and pharmacokinetic profile. Heterocycle optimization and template modification lead to the identification of compound 24 which demonstrated increased atrial effective refractory period in the rabbit pharmacodynamic model with mild effects on blood pressure and heart rate. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.05.035

文献信息

• Design, synthesis and evaluation of phenethylaminoheterocycles as Kv1.5 inhibitors
  作者：James A. Johnson、Ningning Xu、Yoon Jeon、Heather J. Finlay、Alexander Kover、Mary L. Conder、Huabin Sun、Danshi Li、Paul Levesque、Mei-Mann Hsueh、Timothy W. Harper、Ruth R. Wexler、John Lloyd

  DOI：10.1016/j.bmcl.2014.05.035

  日期：2014.7

  Phenethylaminoheterocycles have been prepared and assayed for inhibition of the K(v)1.5 potassium ion channel as a potential approach to the treatment of atrial fibrillation. A diverse set of heterocycles were identified as potent K(v)1.5 inhibitors and were advanced to pharmacodynamic evaluation based on selectivity and pharmacokinetic profile. Heterocycle optimization and template modification lead to the identification of compound 24 which demonstrated increased atrial effective refractory period in the rabbit pharmacodynamic model with mild effects on blood pressure and heart rate. (C) 2014 Elsevier Ltd. All rights reserved.