2-[(2-甲氧基乙基氨基)甲基]恶唑-4-羧酸乙酯 | 1056984-60-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: 2-[(2-甲氧基乙基氨基)甲基]恶唑-4-羧酸乙酯
• 英文名称: 2-[(2-methoxyethylamino)methyl]oxazole-4-carboxylic acid ethyl ester
• 英文别名: Ethyl 2-[(2-methoxyethylamino)methyl]-1,3-oxazole-4-carboxylate
• CAS: 1056984-60-1
• 化学式: C₁₀H₁₆N₂O₄
• 分子量: 228.248
• InChiKey: NCNBCTMNYZUFJA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.1
• 重原子数：
  16
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  73.6
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-[(2-甲氧基乙基氨基)甲基]恶唑-4-羧酸乙酯 在 水 、 sodium hydroxide 作用下， 以 1,4-二氧六环 为溶剂， 反应 15.0h， 生成
  参考文献：
  名称：

  Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

  摘要：

  A series of small molecules consisting of a heterocyclic core flanked by two basic functionalities were synthesized and screened for in vitro affinity at the human histamine H-3 receptor (hH(3)R). Nine of the twenty-eight compounds tested were found to possess a hH(3)R K-i of less than 5 nM and consisted of a diverse range of central hetero-aromatic linkers (pyridine, pyrazine, oxazole, isoxazole, thiazole, furan, thiophene, and pyrrole). One member of this series, (4-isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanone (37), was found to be a high affinity, selective antagonist that crosses the blood-brain barrier and occupies H-3 receptors after oral administration in the rat. (C) 2009 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2009.06.007
• 作为产物：
  描述：

  ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate 、 2-甲氧基乙胺 以 二氯甲烷 为溶剂， 反应 0.5h， 生成 2-[(2-甲氧基乙基氨基)甲基]恶唑-4-羧酸乙酯
  参考文献：
  名称：

  Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

  摘要：

  A series of small molecules consisting of a heterocyclic core flanked by two basic functionalities were synthesized and screened for in vitro affinity at the human histamine H-3 receptor (hH(3)R). Nine of the twenty-eight compounds tested were found to possess a hH(3)R K-i of less than 5 nM and consisted of a diverse range of central hetero-aromatic linkers (pyridine, pyrazine, oxazole, isoxazole, thiazole, furan, thiophene, and pyrrole). One member of this series, (4-isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanone (37), was found to be a high affinity, selective antagonist that crosses the blood-brain barrier and occupies H-3 receptors after oral administration in the rat. (C) 2009 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2009.06.007

文献信息

• Non-imidazole heterocyclic compounds
  申请人：Carruthers I. Nicholas

  公开号：US20050222129A1

  公开（公告）日：2005-10-06

  Certain non-imidazole heterocyclic compounds are histamine H 3 modulators useful in the treatment of histamine H 3 receptor mediated diseases.

  某些非咪唑杂环化合物是组胺H3调节剂，可用于治疗组胺H3受体介导的疾病。
• NON-IMIDAZOLE HETEROCYCLIC COMPOUNDS
  申请人：Carruthers Nicholas I.

  公开号：US20080317671A1

  公开（公告）日：2008-12-25

  Certain non-imidazole heterocyclic compounds are histamine H 3 modulators useful in the treatment of histamine H 3 receptor mediated diseases.

  某些非咪唑杂环化合物是组胺H3调节剂，可用于治疗组胺H3受体介导的疾病。
• NON-IMIDAZOLE HETEROCYCLIC COMPOUNDS AS HISTAMINE H3 RECEPTOR MODULATORS
  申请人：Janssen Pharmaceutica NV

  公开号：EP1771432B1

  公开（公告）日：2010-12-08
• US7429659B2
  申请人：——

  公开号：US7429659B2

  公开（公告）日：2008-09-30