4-(5-Amino-2-chloropyrimidin-4-yl)oxy-3,5-dimethylbenzonitrile | 1303518-47-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-(5-Amino-2-chloropyrimidin-4-yl)oxy-3,5-dimethylbenzonitrile
• 英文别名: 4-(5-amino-2-chloropyrimidin-4-yl)oxy-3,5-dimethylbenzonitrile
• CAS: 1303518-47-9
• 化学式: C₁₃H₁₁ClN₄O
• 分子量: 274.71
• InChiKey: YXUWILZOZJXCGA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  84.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  5-氨基-2,4-二氯嘧啶 、 3,5-二甲基-4-羟基苯甲腈 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 4-(5-Amino-2-chloropyrimidin-4-yl)oxy-3,5-dimethylbenzonitrile
  参考文献：
  名称：

  Exploration of piperidine-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses

  摘要：

  Further investigation of the recently reported piperidine-4-yl-aminopyrimidine class of non-nucleoside reverse transcriptase inhibitors (NNRTIs) has been carried out. Thus, preparation of a series of N-phenyl piperidine analogs resulted in the identification of 3-carboxamides as a particularly active series. Analogs such as 28 and 40 are very potent versus wild-type HIV-1 and a broad range of NNRTI-resistant mutant viruses. Synthesis, structure-activity relationship (SAR), clearance data, and crystallographic evidence for the binding motif are discussed. (c) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.08.068

文献信息

• Exploration of piperidine-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses
  作者：Guozhi Tang、Denis J. Kertesz、Minmin Yang、Xianfeng Lin、Zhanguo Wang、Wentao Li、Zongxing Qiu、Junli Chen、Jianghua Mei、Li Chen、Taraneh Mirzadegan、Seth F. Harris、Armando G. Villaseñor、Jennifer Fretland、William L. Fitch、Julie Qi Hang、Gabrielle Heilek、Klaus Klumpp

  DOI：10.1016/j.bmcl.2010.08.068

  日期：2010.10

  Further investigation of the recently reported piperidine-4-yl-aminopyrimidine class of non-nucleoside reverse transcriptase inhibitors (NNRTIs) has been carried out. Thus, preparation of a series of N-phenyl piperidine analogs resulted in the identification of 3-carboxamides as a particularly active series. Analogs such as 28 and 40 are very potent versus wild-type HIV-1 and a broad range of NNRTI-resistant mutant viruses. Synthesis, structure-activity relationship (SAR), clearance data, and crystallographic evidence for the binding motif are discussed. (c) 2010 Elsevier Ltd. All rights reserved.