(2S,3R)-3-benzyl-2-oxiranecarboxylic acid | 608520-04-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 环氧化物
• 英文名称: (2S,3R)-3-benzyl-2-oxiranecarboxylic acid
• 英文别名: (2S,3R)-3-benzyloxirane-2-carboxylic acid
• CAS: 608520-04-3
• 化学式: C₁₀H₁₀O₃
• 分子量: 178.188
• InChiKey: WFWJUTYQYLLJHM-BDAKNGLRSA-N

物化性质

• 沸点：
  344.9±35.0 °C(Predicted)
• 密度：
  1.321±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  49.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (2S,3R)-3-benzyl-2-oxiranecarboxylic acid 在 copper(II) nitrate sodium tetrahydroborate 、 sodium azide 作用下， 以 水 为溶剂， 反应 2.0h， 生成 (2S,3s)-3-氨基-2-羟基-4-苯基丁酸
  参考文献：
  名称：

  First One-Pot Copper-Catalyzed Synthesis of α-Hydroxy-β-Amino Acids in Water. A New Protocol for Preparation of Optically Active Norstatines

  摘要：

  alpha-Hydroxy-beta-amino acids were synthesized with excellent yields for the first time in water and by a simple procedure based on a copper catalytic cycle, which included the recovery and reuse of the catalyst and is possible to realize by using only water as reaction medium.

  DOI：

  10.1021/jo034752y
• 作为产物：
  描述：

  [(2R,3R)-3-(苯基甲基)环氧乙烷-2-基]甲醇 在 ruthenium trichloride 、 过碘酸 作用下， 生成 (2S,3R)-3-benzyl-2-oxiranecarboxylic acid
  参考文献：
  名称：

  First One-Pot Copper-Catalyzed Synthesis of α-Hydroxy-β-Amino Acids in Water. A New Protocol for Preparation of Optically Active Norstatines

  摘要：

  alpha-Hydroxy-beta-amino acids were synthesized with excellent yields for the first time in water and by a simple procedure based on a copper catalytic cycle, which included the recovery and reuse of the catalyst and is possible to realize by using only water as reaction medium.

  DOI：

  10.1021/jo034752y

文献信息

• Process for production of optically active-3-amino-2-hydroxypropionic cyclopropylamide derivatives and salts thereof
  申请人：Mori Kohei

  公开号：US20100048909A1

  公开（公告）日：2010-02-25

  An objective of the present application is to provide an industrially practicable method for producing an optically-active 3-amino-2-hydroxypropionic cyclopropylamide derivative or salt thereof from an inexpensive easily-available starting material. The derivative or salt thereof is useful as an intermediate for a medicine. It is also intended by the present application to provide a useful intermediate of the derivative. The objective is attained by the following method. First, an easily-available 2-halo-3-oxopropionic acid derivative is asymmetrically reduced, and then epoxidated to produce an optically-active epoxycarboxylic acid derivative. Next, the derivative is converted into an optically-active epoxyamide derivative by reaction with cyclopropylamine, and then reacted with a nitrile to obtain an optically-active oxazolinamide derivative. Subsequently, selective acid solvolysis of the oxazoline skeleton gives the optically-active 3-amino-2-hydroxypropionic cyclopropylamide derivative or salt thereof.

  本申请的目标是提供一种工业实用的方法，从廉价易得的起始物质中生产出光学活性的3-氨基-2-羟基丙酸环丙酰胺衍生物或其盐。该衍生物或其盐可用作药物的中间体。本申请还旨在提供该衍生物的有用中间体。该目标通过以下方法实现。首先，对易得的2-卤代-3-酮丙酸衍生物进行不对称还原，然后环氧化，以产生光学活性的环氧羧酸衍生物。接下来，通过与环丙胺反应将该衍生物转化为光学活性的环氧酰胺衍生物，然后与腈反应得到光学活性的噁唑烷酰胺衍生物。随后，对噁唑烷骨架进行选择性酸性溶解，得到光学活性的3-氨基-2-羟基丙酸环丙酰胺衍生物或其盐。
• Process for preparing optically active allophenylnorstatin derivatives, and intermediates for use therein
  申请人：Takasago International Corporation

  公开号：EP0729939A2

  公开（公告）日：1996-09-04

  A process for preparing an optically active (2S,3S)-allophenylnorstatin derivative (I) is disclosed, comprising asymmetrically hydrogenating a 4-phenyl-2-halogeno-3-oxobutyric ester (III) in the presence of a ruthenium-phosphine complex to obtain a 4-phenyl-(2S)-halogen-(3R)-hydroxybutyric ester (IV), epoxidizing the ester (IV) in the presence of a base to obtain a 4-phenyl-(2S,3R)-epoxybutyric ester (V), reacting the ester (V) with a tri(lower alkyl)silylazide or a (lower alkyl)diarylsilylazide in th epresence of a Lewis Acid to obtain a (3S)-azido-4-phenyl-(2S)-trisubstituted silyloxybutyric ester (VI), hydrogenolyzing the ester (VI) into a (2S,3S)-allophenylnorstatin derivative (VII), protecting the amino group of the compound (VII), and, if desired, hydrolyzing the compound before or after the amino group protection. Compounds (I) can be obtained at high optical purity safely and in good yield.

  本发明公开了一种制备光学活性(2S,3S)-别苯基去甲司他汀衍生物(I)的工艺，包括在钌膦络合物存在下不对称氢化4-苯基-2-卤代-3-氧代丁酸酯(III)，得到4-苯基-(2S)-卤代-(3R)-羟基丁酸酯(IV)、在碱存在下使酯 (IV) 环氧化，得到 4-苯基-(2S,3R)-环氧丁酸酯 (V)在路易斯酸存在下，将酯 (V) 与三(低级烷基)水杨酰肼或(低级烷基)二水杨酰肼反应，得到 (3S)-azido-4-phenyl-(2S)-trisubstituted silyloxybutyric ester (VI)、将酯（VI）氢解为(2S,3S)-别苯基山奈司他丁衍生物（VII），保护化合物（VII）的氨基，如果需要，在氨基保护之前或之后对化合物进行水解。可以安全地获得高光学纯度和高产率的化合物 (I)。
• PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-2 -HYDROXYPROPIONIC CYCLOPROPYLAMIDE DERIVATIVES AND SALTS THEREOF
  申请人：Kaneka Corporation

  公开号：EP2039689A1

  公开（公告）日：2009-03-25

  An objective of the present application is to provide an industrially practicable method for producing an optically-active 3-amino-2-hydroxypropionic cyclopropylamide derivative or salt thereof from an inexpensive easily-available starting material. The derivative or salt thereof is useful as an intermediate for a medicine. It is also intended by the present application to provide a useful intermediate of the derivative. The objective is attained by the following method. First, an easily-available 2-halo-3-oxopropionic acid derivative is asymmetrically reduced, and then epoxidated to produce an optically-active epoxycarboxylic acid derivative. Next, the derivative is converted into an optically-active epoxyamide derivative by reaction with cyclopropylamine, and then reacted with a nitrile to obtain an optically-active oxazolinamide derivative. Subsequently, selective acid solvolysis of the oxazoline skeleton gives the optically-active 3-amino-2-hydroxypropionic cyclopropylamide derivative or salt thereof.

  本申请的目的是提供一种工业上可行的方法，利用廉价易得的起始原料生产具有光学活性的 3-氨基-2-羟基丙酰基环丙基酰胺衍生物或其盐。该衍生物或其盐可用作药物的中间体。本申请的另一个目的是提供一种有用的衍生物中间体。通过以下方法可以达到目的。首先，将一种易得的 2-卤代-3-氧代丙酸衍生物进行不对称还原，然后环氧化，生成一种具有光学活性的环氧羧酸衍生物。接着，该衍生物与环丙胺反应转化为光学活性环氧酰胺衍生物，然后与腈反应得到光学活性噁唑啉酰胺衍生物。随后，对噁唑啉骨架进行选择性酸溶解，得到具有光学活性的 3-氨基-2-羟基丙酸环丙基酰胺衍生物或其盐。
• EP2039689
  申请人：——

  公开号：——

  公开（公告）日：——
• US5581007A
  申请人：——

  公开号：US5581007A

  公开（公告）日：1996-12-03