±-3-(1H-imidazol-1-yl)-1-(thiophen-2-yl)-1-propanol | 1296877-23-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: ±-3-(1H-imidazol-1-yl)-1-(thiophen-2-yl)-1-propanol
• 英文别名: 3-(1H-imidazol-1-yl)-1-(thiophen-2-yl)propan-1-ol；3-Imidazol-1-yl-1-thiophen-2-ylpropan-1-ol
• CAS: 1296877-23-0
• 化学式: C₁₀H₁₂N₂OS
• 分子量: 208.284
• InChiKey: XRGRORDAQZAPFK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  66.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  ±-3-(1H-imidazol-1-yl)-1-(thiophen-2-yl)-1-propanol 、 2,4-二氟溴苄 在 potassium tert-butylate 作用下， 以 二甲基亚砜 为溶剂， 以69%的产率得到1-(3-(2,4-difluorobenzyloxy)-3-(thiophen-2-yl)propyl)-1H-imidazole
  参考文献：
  名称：

  Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents

  摘要：

  A series of benzyloxy furanyl and benzyloxy thiophenyl azoles were synthesized and screened for their in vitro antileishmanial activity against Leishmania donovani. Among all, 16 compounds have shown more than 90% inhibition against promastigotes at 20 mu M while 11 compounds exhibited IC50 in the range of 3.04-9.39 mu M against amastigotes. Compound 4, a 3-chlorobenzyloxy furanyl imidazole emerged as the most active compound in the series with IC50 value of 3.04 mu M and SI value of 19.80, and was several folds more potent than the reference drugs miltefosine and miconazole. (C) 2011 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2011.02.021
• 作为产物：
  描述：

  3-(pyrrolidin-1-yl)-1-(thiophen-2-yl)propan-1-one hydrochloride 在 sodium tetrahydroborate 作用下， 以 甲醇 、 乙醇 、 水 为溶剂， 反应 2.5h， 生成 ±-3-(1H-imidazol-1-yl)-1-(thiophen-2-yl)-1-propanol
  参考文献：
  名称：

  Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents

  摘要：

  A series of benzyloxy furanyl and benzyloxy thiophenyl azoles were synthesized and screened for their in vitro antileishmanial activity against Leishmania donovani. Among all, 16 compounds have shown more than 90% inhibition against promastigotes at 20 mu M while 11 compounds exhibited IC50 in the range of 3.04-9.39 mu M against amastigotes. Compound 4, a 3-chlorobenzyloxy furanyl imidazole emerged as the most active compound in the series with IC50 value of 3.04 mu M and SI value of 19.80, and was several folds more potent than the reference drugs miltefosine and miconazole. (C) 2011 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2011.02.021

文献信息

• A Novel Antifungal Agent with Broad Spectrum: 1-(4-Biphenylyl)-3-(1<i>H</i>-imidazol-1-yl)-1-propanone
  作者：Gheorghe Roman、Mihai Mareş、Valentin Năstasă

  DOI：10.1002/ardp.201200287

  日期：2013.2

  carbonyl function of the imidazole–ketones in the previous series by means of NaBH4. All of the compounds were evaluated for antifungal activity against 16 strains of Candida, and 3‐(1H‐imidazol‐1‐yl)‐1‐(4‐biphenylyl)‐1‐propanone emerged as a broad‐spectrum antifungal agent. Several 3‐(1H‐imidazol‐1‐yl)‐1‐(2′‐(substituted benzyl)oxyphenyl)‐1‐propanones were also active towards Candida kefyr.

  通过咪唑与3-二甲氨基-1-（取代芳基）-1-丙酮盐酸盐的N-烷基化合成一系列（1-取代芳基）-3-（1H-咪唑-1-基）-1-丙酮（酮曼尼希碱）。第二系列 N1 取代的咪唑是通过使用 NaBH4 还原前一系列中咪唑-酮的羰基官能团而获得的。评估了所有化合物对 16 种念珠菌的抗真菌活性，3-(1H-咪唑-1-基)-1-(4-联苯基)-1-丙酮作为广谱抗真菌剂出现。几种 3-(1H-咪唑-1-基)-1-(2'-(取代苄基)氧基苯基)-1-丙酮对克菲尔念珠菌也有活性。
• Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents
  作者：Vijay K. Marrapu、Monika Mittal、Rahul Shivahare、Suman Gupta、Kalpana Bhandari

  DOI：10.1016/j.ejmech.2011.02.021

  日期：2011.5

  A series of benzyloxy furanyl and benzyloxy thiophenyl azoles were synthesized and screened for their in vitro antileishmanial activity against Leishmania donovani. Among all, 16 compounds have shown more than 90% inhibition against promastigotes at 20 mu M while 11 compounds exhibited IC50 in the range of 3.04-9.39 mu M against amastigotes. Compound 4, a 3-chlorobenzyloxy furanyl imidazole emerged as the most active compound in the series with IC50 value of 3.04 mu M and SI value of 19.80, and was several folds more potent than the reference drugs miltefosine and miconazole. (C) 2011 Elsevier Masson SAS. All rights reserved.