2-(2-azidoethoxy)methyl-4-(2-chlorophenyl)-3-(2-hydroxyethoxycarbonyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine | 120300-94-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 2-(2-azidoethoxy)methyl-4-(2-chlorophenyl)-3-(2-hydroxyethoxycarbonyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine
• 英文别名: 3-O-(2-hydroxyethyl) 5-O-methyl 2-(2-azidoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
• CAS: 120300-94-9
• 化学式: C₂₀H₂₃ClN₄O₆
• 分子量: 450.879
• InChiKey: ATQPIFGGBROZNI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.59
• 重原子数：
  31.0
• 可旋转键数：
  10.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  142.85
• 氢给体数：
  2.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  2-(2-azidoethoxy)methyl-4-(2-chlorophenyl)-3-(2-hydroxyethoxycarbonyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine 在 Lindlar's catalyst 氢气 作用下， 以 乙醇 为溶剂， 以57%的产率得到2-(2-aminoethoxy)methyl-4-(2-chlorophenyl)-3-(2-hydroxyethoxycarbonyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine
  参考文献：
  名称：

  Long-acting dihydropyridine calcium antagonists. 9. Structure activity relationships around amlodipine

  摘要：

  The preparation of a range of 1,4-dihydropyridine analogues of amlodipine has been undertaken and their calcium antagonist activities on rat aorta have been evaluated. Increasing the size of the C5 ester group dramatically reduces calcium antagonist activity, a trend which would be compatible with the carbonyl group of that ester binding to the DHP receptor. Amlodipine analogues with extended C3 ester substituents also have lower potency than amlodipine, possibly because of disruption of a favourable interaction between the protonated amino group on the 2-substituent and the DHP receptor. Replacement of the 6-methyl substituent in amlodipine by alkoxyalkyl groups or electron-withdrawing groups is also detrimental to calcium antagonist activity.

  DOI：

  10.1016/0223-5234(91)90132-7
• 作为产物：
  描述：

  2-<(2-azidoethoxy)methyl>-4-(2-chlorophenyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 0.5h， 生成 2-(2-azidoethoxy)methyl-4-(2-chlorophenyl)-3-(2-hydroxyethoxycarbonyl)-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine
  参考文献：
  名称：

  Long-acting dihydropyridine calcium antagonists. 9. Structure activity relationships around amlodipine

  摘要：

  The preparation of a range of 1,4-dihydropyridine analogues of amlodipine has been undertaken and their calcium antagonist activities on rat aorta have been evaluated. Increasing the size of the C5 ester group dramatically reduces calcium antagonist activity, a trend which would be compatible with the carbonyl group of that ester binding to the DHP receptor. Amlodipine analogues with extended C3 ester substituents also have lower potency than amlodipine, possibly because of disruption of a favourable interaction between the protonated amino group on the 2-substituent and the DHP receptor. Replacement of the 6-methyl substituent in amlodipine by alkoxyalkyl groups or electron-withdrawing groups is also detrimental to calcium antagonist activity.

  DOI：

  10.1016/0223-5234(91)90132-7

文献信息

• Beresford; Macrae; Alker, Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 2, p. 201 - 209
  作者：Beresford、Macrae、Alker、Kobylecki

  DOI：——

  日期：——
• BERESFORD, A. P.;MACRAE, P. V.;ALKER, D.;KOBYLECKI, R. J., ARZNEIM.-FORSCH., 39,(1989) N, C. 201-209
  作者：BERESFORD, A. P.、MACRAE, P. V.、ALKER, D.、KOBYLECKI, R. J.

  DOI：——

  日期：——