2-amino-4-(2-thienyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 2-amino-4-(2-thienyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile
• 英文别名: 2-Amino-4-thiophen-2-yl-5,6,7,8-tetrahydroquinoline-3-carbonitrile
• 化学式: C₁₄H₁₃N₃S
• mdl: MFCD00446163
• 分子量: 255.343
• InChiKey: FTKATHYCSFVXJI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  90.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-噻吩甲醛 、 环己酮 、 丙二腈 在 C₂₈H₁₆CoN₁₂O₁₂S₄⁽⁴⁺⁾*4Cl^(1-) 作用下， 以 neat (no solvent) 为溶剂， 反应 0.25h， 以74%的产率得到2-amino-4-(2-thienyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile
  参考文献：
  名称：

  Synthesis of cobalt tetra-2,3-pyridiniumporphyrazinato with sulfonic acid tags as an efficient catalyst and its application for the synthesis of bicyclic ortho-aminocarbonitriles, cyclohexa-1,3-dienamines and 2-amino-3-cyanopyridines

  摘要：

  "ortho"-氨基腈、环己烯-1,3-二胺和2-氨基-3-氰基吡啶通过[Co(TPPASO3H)]Cl作为高效的吡啶基卟啉催化剂合成。

  DOI：

  10.1039/d0ra02172e

文献信息

• An efficient protocol for the one-pot multicomponent synthesis of polysubstituted pyridines by using a biopolymer-based magnetic nanocomposite
  作者：Ali Maleki、Abbas Ali Jafari、Somayeh Yousefi、Vahid Eskandarpour

  DOI：10.1016/j.crci.2015.09.002

  日期：2015.12

  Résumé A biopolymer cellulose-based magnetic composite nanocatalyst was prepared and characterized by using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). Then, it was used efficiently in the multicomponent synthesis of polysubstituted pyridines under mild reaction conditions and using an easy work-up procedure at room temperature in ethanol. The nanocatalyst can be recovered easily and reused several times without significant loss of catalytic activity. Supplementary Materials: Supplementary materials for this article are supplied as separate files: mmc1.doc mmc2.zip mmc3.doc mmc4.doc

  摘要 基于生物聚合物纤维素的磁性复合纳米催化剂通过扫描电子显微镜（SEM）和能量色散X射线光谱（EDX）制备和表征。随后，该催化剂在温和反应条件下，以乙醇为溶剂并在室温下，高效用于多组分合成多取代吡啶。纳米催化剂易于回收，并可重复使用多次而不会显著损失催化活性。 补充材料： 本文的补充材料以单独文件形式提供： mmc1.doc mmc2.zip mmc3.doc mmc4.doc
• Method of using aminocyanopyridine compounds as mitogen activated protein kinase-activated protein kinase-2 inhibitors
  申请人：Pharmacia Corporation

  公开号：US20040127519A1

  公开（公告）日：2004-07-01

  A method is described for inhibiting mitogen activated protein kinase-activated protein kinase-2 in a subject in need of such inhibition, where the method involves administering to the subject an anminocyanopyridine MK-2 inhibiting compound, or a pharmaceutically acceptable salt thereof.

  本文描述了一种抑制需要抑制的受试者中的有丝分裂原活化蛋白激酶激活蛋白激酶-2的方法，其中该方法涉及向受试者给予一种抑制MK-2的氨基氰基吡啶化合物或其药学上可接受的盐。
• Aminocyanopyridine inhibitors of mitogen activated protein kinase-activated protein kinase-2
  申请人：Pharmacia Corporation

  公开号：US20040142978A1

  公开（公告）日：2004-07-22

  Aminocyanopyridine compounds are described which can inhibit mitogen activated protein kinase-activated protein kinase-2. Pharmaceutical compositions and kits that contain these compounds are also described.

  描述了可抑制丝裂原活化蛋白激酶-活化蛋白激酶-2 的氨基氰吡啶化合物。还描述了含有这些化合物的药物组合物和试剂盒。
• ELGEMEIE, GALAL E. H., SULFUR. LETT., 9,(1989) N, C. 253-264
  作者：ELGEMEIE, GALAL E. H.

  DOI：——

  日期：——
• METHOD OF USING AMINOCYANOPYRIDINE COMPOUNDS AS MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2 INHIBITORS
  申请人：Pharmacia Corporation

  公开号：EP1569645A2

  公开（公告）日：2005-09-07