5-benzyl-4-(4-fluorophenyl)-N-(4-methoxybenzyl)thiazol-2-amine | 1446018-11-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-benzyl-4-(4-fluorophenyl)-N-(4-methoxybenzyl)thiazol-2-amine
• 英文别名: 5-benzyl-4-(4-fluorophenyl)-N-[(4-methoxyphenyl)methyl]thiazol-2-amine；5-benzyl-4-(4-fluorophenyl)-N-[(4-methoxyphenyl)methyl]-1,3-thiazol-2-amine
• CAS: 1446018-11-6
• 化学式: C₂₄H₂₁FN₂OS
• 分子量: 404.508
• InChiKey: QEYGPVIRCKKUNG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  29
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  62.4
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  4-氟苯乙酮 在 aluminum (III) chloride 、 sodium tetrahydroborate 、 palladium on activated charcoal 、 氢气 、 溴 、 sodium acetate 、 对甲苯磺酸 、 sodium hydroxide 作用下， 以 乙醇 、 氯仿 、 水 、 乙酸乙酯 、 甲苯 为溶剂， 反应 6.17h， 生成 5-benzyl-4-(4-fluorophenyl)-N-(4-methoxybenzyl)thiazol-2-amine
  参考文献：
  名称：

  2,4,5-Trisubstituted thiazole derivatives: A novel and potent class of non-nucleoside inhibitors of wild type and mutant HIV-1 reverse transcriptase

  摘要：

  Novel 2,4,5-trisubstituted thiazole derivatives (TSTs) were designed and synthesized as HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). Among the thirty-eight synthesized target compounds, thirty TSTs showed potent inhibition against HIV-1 replication in wild type HIV-1 at submicromolar concentrations (from 0.046 to 9.59 mu M). Compounds 21, 23 and 24 were also tested on seven NNRTI-resistant HIV-1 strains, and all exhibited inhibitory effects with fold changes in IC50 ranging from 2.6 to 111, which were better than those of nevirapine (15.6-fold-371-fold). Docking simulations of compound 24 revealed a reasonable mechanism for the binding mode, and three-dimensional quantitative structure activity relationship (3-DQSAR) studies on this novel series of TST further elucidated the structure-activity relationship (SAR). The results suggested the great potential of TSTs as a novel class of NNRTIs with antiviral efficacy and a good resistance profile. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.07.072