5-(6-fluoro-1H-benzimidazol-2-yl)-2'-deoxyuridine | 1354943-57-9

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘧啶核苷
• 英文名称: 5-(6-fluoro-1H-benzimidazol-2-yl)-2'-deoxyuridine
• 英文别名: 5-(6-fluoro-1H-benzimidazol-2-yl)-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
• CAS: 1354943-57-9
• 化学式: C₁₆H₁₅FN₄O₅
• 分子量: 362.317
• InChiKey: RBSNFJOAVHZBAD-YNEHKIRRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  26
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  128
• 氢给体数：
  4
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  3,5-双-o-(t-丁基二甲基甲硅烷基)胸腺嘧啶脱氧核苷 在 2,6-二甲基吡啶 、 dipotassium peroxodisulfate 、 copper(ll) sulfate pentahydrate 、 四丁基氟化铵 、 水 、 sodium hydrogensulfite 作用下， 以 四氢呋喃 、 水 、 乙腈 为溶剂， 反应 3.03h， 生成 5-(6-fluoro-1H-benzimidazol-2-yl)-2'-deoxyuridine
  参考文献：
  名称：

  Efficient microwave-assisted synthesis, antibacterial activity and high fluorescence of 5 benzimidazolyl-2′-deoxyuridines

  摘要：

  A series of novel C-5 benzimidazolyl-2'-deoxyuridines was synthesized in good yields under solvent-free conditions and microwave irradiation from 5-formyl-2'-deoxyuridine and arylenediamine derivatives in the presence of NaHSO3 as catalyst. Their absorption and fluorescence spectra were measured. They showed intense fluorescence around 400-500 nm with quantum yields between 0.3 and 0.5. All compounds studied in this work were screened for their antibacterial activities against a series of Gram positive and negative bacteria. The trifluoromethyl substituted benzimidazole derivatives showed some antibacterial activity. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.10.041

文献信息

• Efficient microwave-assisted synthesis, antibacterial activity and high fluorescence of 5 benzimidazolyl-2′-deoxyuridines
  作者：Jamal Krim、Christian Grünewald、Moha Taourirte、Joachim W. Engels

  DOI：10.1016/j.bmc.2011.10.041

  日期：2012.1

  A series of novel C-5 benzimidazolyl-2'-deoxyuridines was synthesized in good yields under solvent-free conditions and microwave irradiation from 5-formyl-2'-deoxyuridine and arylenediamine derivatives in the presence of NaHSO3 as catalyst. Their absorption and fluorescence spectra were measured. They showed intense fluorescence around 400-500 nm with quantum yields between 0.3 and 0.5. All compounds studied in this work were screened for their antibacterial activities against a series of Gram positive and negative bacteria. The trifluoromethyl substituted benzimidazole derivatives showed some antibacterial activity. (C) 2011 Elsevier Ltd. All rights reserved.