3-amino-6-N,N-diethylamino-2-methoxypyridine | 1095033-53-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 3-amino-6-N,N-diethylamino-2-methoxypyridine
• 英文别名: N²,N²-diethyl-6-methoxypyridine-2,5-diamine； N²,N²-diethyl-6-methoxypyridine-2,5-diamine；2-N,2-N-diethyl-6-methoxypyridine-2,5-diamine
• CAS: 1095033-53-6
• 化学式: C₁₀H₁₇N₃O
• 分子量: 195.264
• InChiKey: YBGMQEWVESAEHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  51.4
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-amino-6-N,N-diethylamino-2-methoxypyridine 、 N-(2-((2,5-dichloropyrimidin-4-yl)amino)phenyl)cyclopropanesulfonamide 在 对甲苯磺酸 作用下， 以 异丙醇 为溶剂， 以75.3%的产率得到N-(2-((5-chloro-2-((6-(diethylamino)-2-methoxypyridin-3-yl)amino)pyrimidin-4-yl)amino)phenyl)cyclopropanesulfonamide
  参考文献：
  名称：

  Dual potent ALK and ROS1 inhibitors combating drug-resistant mutants: Synthesis and biological evaluation of aminopyridine-containing diarylaminopyrimidine derivatives

  摘要：

  To identify ALK and ROS1 dual inhibitors conferring resistance to ALK secondary mutations, especially 'gatekeeper' L1196 M and the most predominant ceritinib-resistant G1202R mutations, a series of novel 2,4-diarylaminopyrimidine analogues were designed and synthesized by incorporating 2-alkoxy-6-alicyclic aminopyridinyl motifs. The biological evaluations on cellular and enzymatic assays led to identification of compound F-1, which turned out to be effective against ALK(WT), ROS1(WT), ALK(L1196M) and ALK(G1202R) kinases with IC50 of 2.1 nM, 2.3 nM, 1.3 nM and 3.9 nM, respectively, superior to crizotinib and ceritinib. Moreover, F-1 exhibited significant cytotoxicity on ALK-addicted Karpas299, H2228, and Ba/F3 cell expressing G1202R mutant, as well as ROS1-positive HCC78 cell with IC50 values ranging from 10 nM to 43 nM. Notably, F-1 was capable of suppressing phospho-ALK and its relative downstream signaling pathways, and eventually, inducing cell apoptosis in a dose-dependent manner in Karpas-299 cell. Together, F-1 is validated as a promising ALK/ROS1 dual inhibitor great potential for G1202R ALK mutation cancers. (C) 2018 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2018.09.012
• 作为产物：
  描述：

  N,N-二乙基-5-硝基吡啶-2-胺 在 盐酸 、 tin(II) chloride dihdyrate 、 sodium nitrite 作用下， 以 甲醇 、 水 为溶剂， 反应 50.84h， 生成 3-amino-6-N,N-diethylamino-2-methoxypyridine
  参考文献：
  名称：

  5-叠氮基-2-氨基吡啶，一种新的氮/氮离子光亲和标记剂，在单线态和三线态氮烯之间表现出可逆的系统间交叉

  摘要：

  在非质子和质子溶剂中使用飞秒到微秒瞬态吸收和产物分析结合 ab 研究了一种新的光亲和标记 (PAL) 试剂 5-叠氮基-2-(N,N-二乙氨基)吡啶的光化学initio 多构型和多参考量子化学计算。激发的单线态 S1 态在光谱上是暗的，而对更高位单线态的激发态 S2 和 S3 的光激发通过到 S1 的两个锥形交叉点将光化学反应驱动到无障碍的超快弛豫路径，其中 N2 消除导致形成闭壳单线态氮烯。单线态氮烯在非质子和质子溶剂中经历系统间交叉 (ISC) 到三线态氮烯以及质子化以形成氮离子。非质子溶剂中的 ISC 速率常数随溶剂极性而增加，显示出“直接”间隙效应，而在质子溶剂中观察到“反向”间隙效应。瞬态吸收光度计实验表明，在几十皮秒的时间尺度上会产生 20% 到 50% 的氮鎓离子的溶剂依赖性部分。闭壳单线态氮烯和三线态氮烯在质子溶剂中被一个小的能隙隔开。结果，未反应的三线态氮烯经历延迟的热活化反向

  DOI：

  10.1021/ja405637b

文献信息

• Design, synthesis and biological evaluation N2-(2-alkyoxy-6-aliphatic aminopyridin-3-yl)-2,4-diaminepyrimidine derivatives bearing acylamino or DBTD ‘head’ as potential ALK inhibitors
  作者：Lingyun Xing、Tongfei Jing、Junlong Zhang、Ming Guo、Xiuqi Miao、Feng Jiang、Xin Zhai

  DOI：10.1016/j.bioorg.2018.09.019

  日期：2018.12

  Aiming to develop promising ALK inhibitors, two series of N-2-(2-alkyoxy-6-aliphatic aminopyridin-3-yl)-2,4-diaminepyrimidine derivatives (22a-x and 23a-d) were designed according to scaffold hopping and bioisosterism principles. All compounds were efficiently synthesized by concise reactions and anti-proliferative activities on ALK-addicted H2228, Karpas299 cells and EGFR-expressive A549 cell were evaluated by MTT assay. Several compounds exhibited potential cytotoxic activities with IC50 values below 0.10 mu M. Five compounds (22g, 22h, 22l, 22s and 23a) were selected for further enzymatic determination, resulting in the discovery of 22l against ALK and ALK(L1196M) with IC50 values of 2.1 nM and 3.8 nM. Particularly, western blot and cell apoptosis assays identified 22l as a promising ALK inhibitor, which was capable of obviously inhibiting cellular ALK activity and inducing cell apoptosis. Eventually, molecular docking modes of 22l with ALK confirmed structural basis in accordance with the SARs analysis.