4,6-dimethoxy-2-phenylpyrimidine | 4319-73-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4,6-dimethoxy-2-phenylpyrimidine
• 英文别名: 4,6-dimethoxy-2-phenyl-pyrimidine；2-Phenyl-4,6-dimethoxy-pyrimidin；4,6-Dimethoxy-2-phenyl-pyrimidin；Pyrimidine, 4,6-dimethoxy-2-phenyl-
• CAS: 4319-73-7
• 化学式: C₁₂H₁₂N₂O₂
• 分子量: 216.239
• InChiKey: QZZAQLMQIBMMNA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  44.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-benzoylamino-1-cyano-2-thioxoethylidenetriphenylphosphorane 在 盐酸 、 sodium hydroxide 、 五氯化磷 、 三乙胺 、 三氯氧磷 作用下， 以 甲醇 为溶剂， 反应 22.0h， 生成 4,6-dimethoxy-2-phenylpyrimidine
  参考文献：
  名称：

  Smolii, O. B.; Panchishin, S. Ya.; Drach, B. S., Russian Journal of General Chemistry, 1993, vol. 63, # 9.1, p. 1390 - 1393

  摘要：

  DOI：

文献信息

• Novel Peptidomimetic Hepatitis C Virus NS3/4A Protease Inhibitors Spanning the P2–P1′ Region
  作者：Anna K. Lampa、Sara M. Bergman、Sofia S. Gustafsson、Hiba Alogheli、Eva B. Åkerblom、Gunnar G. Lindeberg、Richard M. Svensson、Per Artursson、U. Helena Danielson、Anders Karlén、Anja Sandström

  DOI：10.1021/ml400217r

  日期：2014.3.13

  Herein, novel hepatitis C virus NS3/4A protease inhibitors based on a P2 pyrimidinyloxyphenylglycine in combination with various regioisomers of an aryl acyl sulfonamide functionality in P1 are presented. The P1' 4-(trifluoromethyl)phenyl side chain was shown to be particularly beneficial in terms of inhibitory potency. Several inhibitors with K i-values in the nanomolar range were developed and included identification of promising P3-truncated inhibitors spanning from P2-P1'. Of several different P2 capping groups that were evaluated, a preference for the sterically congested Boc group was revealed. The inhibitors were found to retain inhibitory potencies for A156T, D168V, and R155K variants of the protease. Furthermore, in vitro pharmacokinetic profiling showed several beneficial effects on metabolic stability as well as on apparent intestinal permeability from both P3 truncation and the use of the P1' 4-(trifluoromethyl)phenyl side chain.