2-(6-chloro-7-(methoxymethyl)-1H-inden-3-yl)-1H-imidazole | 1231747-39-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚和异茚
• 英文名称: 2-(6-chloro-7-(methoxymethyl)-1H-inden-3-yl)-1H-imidazole
• CAS: 1231747-39-9
• 化学式: C₁₄H₁₃ClN₂O
• 分子量: 260.723
• InChiKey: GXACFQTVOLKASH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  37.91
• 氢给体数：
  1.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  2-(6-chloro-7-(methoxymethyl)-1H-inden-3-yl)-1H-imidazole 在 [(S)-2,2'-双(二苯基磷)-1,1'-联萘]二氯化钌(II) 、 氢气 作用下， 以 甲醇 为溶剂， 20.0 ℃ 、689.49 kPa 条件下， 反应 18.0h， 以85%的产率得到2-(5-chloro-4-(methoxymethyl)-2,3-dihydro-1H-inden-1-yl)-1H-imidazole
  参考文献：
  名称：

  A concise synthesis of chiral indanes as α 1A adrenoceptor partial agonists

  摘要：

  The synthesis of a series of chiral indanes with reported am partial agonist activity is outlined, applying a rhodium catalysed cyclisation for template construction. This method was extended to the asymmetric synthesis of lead compound PF-03774076 (1) which was prepared on >20 g scale in seven steps. Highlights include Rh-mediated cyclocarbonylation and an asymmetric alkene hydrogenation. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2015.10.004
• 作为产物：
  描述：

  2-(6-chloro-7-(methoxymethyl)-1H-inden-3-yl)-N,N-dimethyl-1H-imidazole-1-sulfonamide 在 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 1.0h， 以81%的产率得到2-(6-chloro-7-(methoxymethyl)-1H-inden-3-yl)-1H-imidazole
  参考文献：
  名称：

  A concise synthesis of chiral indanes as α 1A adrenoceptor partial agonists

  摘要：

  The synthesis of a series of chiral indanes with reported am partial agonist activity is outlined, applying a rhodium catalysed cyclisation for template construction. This method was extended to the asymmetric synthesis of lead compound PF-03774076 (1) which was prepared on >20 g scale in seven steps. Highlights include Rh-mediated cyclocarbonylation and an asymmetric alkene hydrogenation. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2015.10.004

文献信息

• An improved synthesis of a novel α1A partial agonist including a new two-step synthesis of 4-fluoropyrazole
  作者：Katherine England、Helen Mason、Rachel Osborne、Lee Roberts

  DOI：10.1016/j.tetlet.2010.03.080

  日期：2010.5

  This Letter outlines a new two-step process for the synthesis of 4-fluoropyrazole and its application in an improved synthesis of 4-fluoro-1-[5-fluoro-1-(1H-imidazol-2-yl)-indan-4-ylmethyl]-1H-pyrazole. The original synthesis of 4-fluoro-1-[5-fluoro-1-(1H-imidazol-2-yl)-indan-4-ylmethyl]-1H-pyrazole is also described.

  这封信概述了4-氟吡唑的合成新的两步法及其在4-氟-1- [5-氟-1-（1 H-咪唑-2-基）-茚满- 4-基甲基] -1 H-吡唑。还描述了4-氟-1- [5-氟-1-（1 H-咪唑-2-基）-茚满-4-基甲基] -1 H-吡唑的原始合成。