6-Chloro-1-methyl-1,2,3,4-tetrahydroisoquinoline | 269402-44-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢异喹啉
• 英文名称: 6-Chloro-1-methyl-1,2,3,4-tetrahydroisoquinoline
• CAS: 269402-44-0
• 化学式: C₁₀H₁₂ClN
• mdl: MFCD20542600
• 分子量: 181.665
• InChiKey: MPXZXQCXHQSKAT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  6-Chloro-1-methyl-1,2,3,4-tetrahydroisoquinoline 、 4-Chloro-2-[(4-fluorophenyl)methyl]-5,6-dimethylpyrimidine 在 三乙胺 、 盐酸 作用下， 以 N,N-二甲基甲酰胺 、 乙酸乙酯 为溶剂， 反应 7.0h， 生成 6-chloro-2-[2-[(4-fluorophenyl)methyl]-5,6-dimethylpyrimidin-4-yl]-1-methyl-3,4-dihydro-1H-isoquinoline;hydrochloride
  参考文献：
  名称：

  Novel pyrimidines as acid pump antagonists (APAs)

  摘要：

  A series of pyrimidine derivatives as acid pump antagonists (APAs) was synthesized and the inhibitory activities against H+/K+ ATPase isolated from hog gastric mucosa were determined. After elaborating on substituents at C2 and C4 position of the pyrimidine scaffold, we have observed that the compound 7h is a potent APA with H+/K+ ATPase, IC50 = 52 nM. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.08.007

文献信息

• NOVEL PYRIMIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF
  申请人：YUHAN CORPORATION, LTD.

  公开号：EP1131312A1

  公开（公告）日：2001-09-12
• [EN] NOVEL PYRIMIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF<br/>[FR] NOUVEAUX DERIVES DE PYRIMIDINE ET LEURS PROCEDES DE PREPARATION
  申请人：YUHAN CORP

  公开号：WO2000029403A1

  公开（公告）日：2000-05-25

  The present invention relates to novel pyrimidine derivatives and pharmaceutically acceptable non-toxic salts thereof which possess an excellent inhibitory activity against gastric acid secretion, a pharmaceutical composition containing the same as an active ingredient, and a process for the preparation thereof.
• Novel pyrimidines as acid pump antagonists (APAs)
  作者：Young Ae Yoon、Chan Sun Park、Myung Hun Cha、Hyunho Choi、Jae Young Sim、Jae Gyu Kim

  DOI：10.1016/j.bmcl.2010.08.007

  日期：2010.10

  A series of pyrimidine derivatives as acid pump antagonists (APAs) was synthesized and the inhibitory activities against H+/K+ ATPase isolated from hog gastric mucosa were determined. After elaborating on substituents at C2 and C4 position of the pyrimidine scaffold, we have observed that the compound 7h is a potent APA with H+/K+ ATPase, IC50 = 52 nM. (C) 2010 Elsevier Ltd. All rights reserved.