(S)-3-氨基-3-苯基-1-丙醇盐酸盐 | 936499-93-3

• 物质功能分类: 医药中间体 - 原料药中间体
• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: (S)-3-氨基-3-苯基-1-丙醇盐酸盐
• 英文名称: (S)-3-amino-3-phenylpropan-1-ol hydrochloride
• 英文别名: (3S)-3-amino-3-phenylpropan-1-ol;hydrochloride
• CAS: 936499-93-3
• 化学式: C₉H₁₃NO*ClH
• 分子量: 187.669
• InChiKey: VPSAJDGAYRBFPH-FVGYRXGTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.49
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  46.2
• 氢给体数：
  3
• 氢受体数：
  2

安全信息

• 海关编码：
  2922199090

反应信息

• 作为反应物：
  描述：

  (S)-3-氨基-3-苯基-1-丙醇盐酸盐 在 吡啶 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 methanesulfonic acid (S)-3-tert-butoxycarbonylamino-3-phenylpropyl ester
  参考文献：
  名称：

  BRANCHED OXATHIAZINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICINE AND DRUG CONTAINING SAID DERIVATIVES AND USE THEREOF

  摘要：

  该发明涉及公式(I)的化合物及其生理相容盐。所述化合物适用于治疗高血糖，例如。

  公开号：

  US20130345126A1
• 作为产物：
  描述：

  3-氨基-3-苯基-1-丙醇 在 盐酸 、 sodium hydroxide 、 phosphate buffer 、 penicillin G acylase immobilized on epoxy-resin 作用下， 以 乙醇 、 水 为溶剂， 反应 5.0h， 生成 (S)-3-氨基-3-苯基-1-丙醇盐酸盐
  参考文献：
  名称：

  Preparation of enantiomerically pure (R)- and (S)-3-amino-3-phenyl-1-propanol via resolution with immobilized penicillin G acylase

  摘要：

  Ethyl 2,4-dioxo-4-phenylbutyrate, obtained by condensation of acetophenone with diethyl oxalate, was converted to 3-oxo-3-phenyl-1-propanol in 90% yield by reaction with baker's yeast. Reductive amination with sodium cyanoborohydride in the presence of ammonium acetate gave the racemic 3-amino-3-phenyl-1-propanol in 65% yield. Enzymatic resolution of the corresponding N-phenylacetyl derivative with penicillin G acylase, immobilized on an epoxy resin gave (S)-amide and (R)-amino alcohol in high enantiomeric purity (ee > 99%) and > 45% yields for each enantiomer. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2005.12.022

文献信息

• [EN] PYRROLO [2, 3 -D] PYRIMIDIN DERIVATIVES AS PROTEIN KINASE B INHIBITORS<br/>[FR] DÉRIVÉS PYRROLO[2,3-D]PYRIMIDINE COMME INHIBITEURS DE LA PROTÉINE KINASE B
  申请人：ASTRAZENECA AB

  公开号：WO2009047563A1

  公开（公告）日：2009-04-16

  The invention relates to a novel group of compounds of Formula (I) or salts thereof: wherein Y, Z1, Z2, R1, R4, R5 and n are as described in the specification, which may be useful in the treatment or prevention of a disease or medical condition mediated through protein kinase B (PKB) such as cancer. The invention also relates to pharmaceutical compositions comprising said compounds, methods of treatment of diseases mediated by PKB using said compounds and methods for preparing compounds of Formula (I).

  该发明涉及一类新型化合物，其化学式为（I）或其盐：其中Y、Z1、Z2、R1、R4、R5和n如规范中所述，这些化合物可能在通过蛋白激酶B（PKB）介导的疾病或医疗状况的治疗或预防中有用，例如癌症。该发明还涉及包含所述化合物的药物组合物，使用所述化合物治疗通过PKB介导的疾病的方法，以及制备化合物（I）的方法。
• A Practical Electrophilic Nitrogen Source for the Synthesis of Chiral Primary Amines by Copper-Catalyzed Hydroamination
  作者：Sheng Guo、Jeffrey C. Yang、Stephen L. Buchwald

  DOI：10.1021/jacs.8b10564

  日期：2018.11.21

  and practical method for the catalytic installation of the amino group across alkenes and alkynes has long been recognized as a significant challenge in synthetic chemistry. As the direct hydroamination of olefins using ammonia requires harsh conditions, the development of suitable electrophilic aminating reagents for formal hydroamination methods is of importance. Herein, we describe the use of 1

  在烯烃和炔烃之间催化安装氨基的温和实用方法长期以来一直被认为是合成化学中的重大挑战。由于使用氨直接对烯烃加氢胺化需要苛刻的条件，因此为正式加氢胺化方法开发合适的亲电胺化试剂具有重要意义。在此，我们描述了使用 1,2-苯并异恶唑作为实用的亲电伯胺源。使用这种杂环作为新的氨基传递剂，开发了一种温和的通用方案，用于氢化铜催化烯烃和炔烃的加氢胺化以形成伯胺。该方法提供了获得广泛的手性 α-支化伯胺和线性伯胺的途径，
• DI- AND TRI-SUBSTITUTED OXATHIAZINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICINE AND DRUG CONTAINING SAID DERIVATIVES AND USE THEREOF
  申请人：Boehme Thomas

  公开号：US20130345125A1

  公开（公告）日：2013-12-26

  The invention relates to compounds of formula (I) and to the physiologically compatible salts thereof. Said compounds are suitable, for example, for treating hyperglycemia.

  该发明涉及式(I)的化合物及其生理兼容盐。所述化合物适用于治疗高血糖，例如。
• DI AND TRI - SUBSTITUTED OXATHIAZINE DERIVATIVES, METHOD FOR THE PRODUCTION, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICINE AND DRUG CONTAINING SAID DERIVATIVES AND USE THEREOF
  申请人：Boehme Thomas

  公开号：US20130338150A1

  公开（公告）日：2013-12-19

  The invention relates to compounds of formula (I) and to the physiologically compatible salts thereof. Said compounds are suitable, for example, for treating hyperglycemia.

  该发明涉及公式（I）的化合物及其生理兼容盐。这些化合物适用于治疗高血糖，例如。
• TETRASUBSTITUTED OXATHIAZINE DERIVATIVES, METHOD FOR PRODUCING THEM, THEIR USE AS MEDICINE AND DRUG CONTAINING SAID DERIVATIVES AND THE USE THEREOF
  申请人：Boehme Thomas

  公开号：US20140024584A1

  公开（公告）日：2014-01-23

  The invention relates to the compounds of formula (I) and to the physiologically acceptable salts thereof. Said compounds are suitable e.g. for the treatment of hyperglycemia.

  该发明涉及式(I)的化合物以及其生理上可接受的盐。所述化合物适用于治疗高血糖等情况。