(R)-6-bromochroman-2-carboxylic acid | 474111-15-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: (R)-6-bromochroman-2-carboxylic acid
• 英文别名: (2R)-6-bromo-3,4-dihydro-2H-chromene-2-carboxylic acid
• CAS: 474111-15-4
• 化学式: C₁₀H₉BrO₃
• 分子量: 257.084
• InChiKey: LDOBEICKZURYCC-SECBINFHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  methyl (R)-6-bromo-4-oxochroman-2-carboxylate 在 三乙基硅烷 、 三氟乙酸 、 lithium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 水 为溶剂， 反应 8.0h， 生成 (R)-6-bromochroman-2-carboxylic acid
  参考文献：
  名称：

  An efficient and practical enantiospecific synthesis of methyl chromanone- and chroman-2-carboxylates

  摘要：

  Chromanone-2-carboxylates and chroman-2-carboxylates are useful building blocks for the synthesis of a variety of bioactive compounds, such as repinotan, fidarestat, and nebivolol. An efficient and practical enantiospecific synthesis of chromanone-2-carboxylates and chroman-2-carboxylates has been accomplished using intramolecular Mitsunobu etherification of methyl (S)-2-hydroxy-4-oxo-4-(2'-hydroxy)phenylbutanoates derived from L-malic acid. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2015.07.006

文献信息

• 2,6-Substituted chroman derivatives useful as beta-3 adrenoreceptor agonists
  申请人：——

  公开号：US20030078260A1

  公开（公告）日：2003-04-24

  This invention relates to novel 2,6-substituted chroman derivatives which are useful in the treatment of beta-3 adrenoreceptor-mediated conditions.

  这项发明涉及新颖的2,6-取代的色苷衍生物，可用于治疗β-3肾上腺素受体介导的疾病。
• US6660752B2
  申请人：——

  公开号：US6660752B2

  公开（公告）日：2003-12-09
• US6919371B2
  申请人：——

  公开号：US6919371B2

  公开（公告）日：2005-07-19
• An efficient and practical enantiospecific synthesis of methyl chromanone- and chroman-2-carboxylates
  作者：Dong Woon Kim、Md. Maqusood Alam、Young Hun Lee、M. Naseer A. Khan、Yong Zhang、Yong Sup Lee

  DOI：10.1016/j.tetasy.2015.07.006

  日期：2015.9

  Chromanone-2-carboxylates and chroman-2-carboxylates are useful building blocks for the synthesis of a variety of bioactive compounds, such as repinotan, fidarestat, and nebivolol. An efficient and practical enantiospecific synthesis of chromanone-2-carboxylates and chroman-2-carboxylates has been accomplished using intramolecular Mitsunobu etherification of methyl (S)-2-hydroxy-4-oxo-4-(2'-hydroxy)phenylbutanoates derived from L-malic acid. (C) 2015 Elsevier Ltd. All rights reserved.