N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol | 79069-15-1

• 物质功能分类: 生物化工 - 氨基酸及其衍生物 - BOC-氨基酸
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol
• 英文别名: tert-butyl (R)-(1-(benzyloxy)-3-hydroxypropan-2-yl)carbamate；(R)-(+)-3-Benzyloxy-2-(Boc-amino)-1-propanol；tert-butyl N-[(2R)-1-hydroxy-3-phenylmethoxypropan-2-yl]carbamate
• CAS: 79069-15-1
• 化学式: C₁₅H₂₃NO₄
• 分子量: 281.352
• InChiKey: MSIDLARYVJJEQY-CYBMUJFWSA-N

物化性质

• 熔点：
  66-69 °C(lit.)
• 比旋光度：
  -14 º (c=1 in chloroform)
• 沸点：
  443.1±40.0 °C(Predicted)
• 密度：
  1.105
• 溶解度：
  溶于氯仿、二氯甲烷、乙酸乙酯、DMSO、丙酮等。

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  20
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  67.8
• 氢给体数：
  2
• 氢受体数：
  4

安全信息

• WGK Germany：
  3
• 海关编码：
  2924299090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

反应信息

• 作为反应物：
  描述：

  N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol 在 盐酸 作用下， 以 乙酸乙酯 为溶剂， 反应 3.0h， 以79%的产率得到(R)-2-氨基-3-苄氧基-1-丙醇盐酸盐
  参考文献：
  名称：

  Synthesis and evaluation of novel modified γ-lactam prostanoids as EP4 subtype-selective agonists

  摘要：

  To identify chemically and metabolically stable subtype-selective EP4 agonists, design and synthesis of a series of modified gamma-lactam prostanoids has been continued. Prostanoids bearing 2-oxo-1,3-oxazolidine, 2-oxo-1,3-thiazolidine and 5-thioxopyrrolidine as a surrogate for the gamma-hydroxycyclopentanone without a troublesome 11-hydroxy group were identified as highly subtype-selective EP4 agonists. Among the tested, several representative compounds demonstrated in vivo efficacy after oral dosing in rats. Their pharmacokinetic and structure-activity relationship studies are presented. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.12.009
• 作为产物：
  描述：

  2,5-dioxopyrrolidin-1-yl O-benzyl-N-t-butoxycarbonyl-L-serinate 在 sodium tetrahydroborate 作用下， 以 四氢呋喃 为溶剂， 生成 N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol
  参考文献：
  名称：

  8-AZAPROSTAGLANDIN DERIVATIVE COMPOUNDS AND DRUGS CONTAINING THE COMPOUNDS AS THE ACTIVE INGREDIENT

  摘要：

  公开号：

  EP1481976B1

文献信息

• [EN] PENICILLIN-BINDING PROTEIN INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINE DE LIAISON À LA PÉNICILLINE
  申请人：VENATORX PHARMACEUTICALS INC

  公开号：WO2019226931A1

  公开（公告）日：2019-11-28

  Described herein are certain boron-containing compounds, compositions, preparations and their use as modulators of the transpeptidase function of bacterial penicillin-binding proteins and as antibacterial agents. In some embodiments, the compounds described herein inhibit penicillin-binding proteins. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.

  本文描述了某些含硼化合物、组合物、制剂及其作为细菌青霉素结合蛋白的跨肽酶功能调节剂和抗菌剂的用途。在某些实施例中，本文描述的化合物抑制青霉素结合蛋白。在某些实施例中，本文描述的化合物在治疗细菌感染方面是有用的。
• NOVEL COMPOUNDS FOR MEDICAL USE AS PEPTIDASE EFFECTORS
  申请人：ANSORGE Siegfried

  公开号：US20120028995A1

  公开（公告）日：2012-02-02

  The invention relates to compounds of general formula (I) as set forth in the claims as well as to the use of the compounds of the general formula (1) in the medical field, specifically for use in the suppression of DNA synthesis and inflammatory cytokine production as well as in the stimulation of anti-inflammatory cytokine production in vitro and in vivo. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.

  该发明涉及一般式（I）所述的化合物，以及该一般式（1）化合物在医学领域中的使用，具体用于抑制DNA合成和炎症细胞因子的产生，以及在体外和体内刺激抗炎细胞因子的产生。本摘要既不旨在定义本说明书中披露的发明，也不旨在以任何方式限制发明的范围。
• Synthesis of N-urethane Protected β-Amino Alcohols Employing <i>N</i>-(protected-α-aminoacyl)benzotriazoles
  作者：Vommina V. Sureshbabu、N.S. Sudarshan、L. Muralidhar、N. Narendra

  DOI：10.3184/030823407x272985

  日期：2007.12

  A simple and racemisation-free synthesis of N-urethane protected α-amino/peptidyl alcohols by the reduction of the corresponding easily accessible N-acylbenzotriazoles is described. The method is practical, straightforward, fast and efficient for the synthesis of amino/peptidyl alcohols. All the alcohols made were isolated in high yields and purity.

  通过还原相应的易于获得的 N-酰基苯并三唑，描述了一种简单且无外消旋化的 N-氨基/肽基醇的合成方法。该方法实用、直接、快速、高效，适用于合成氨基/肽醇。所有制得的醇都以高产率和高纯度分离出来。
• 3-(2-Acylamino-1-Hydroxyethyl)-Morpholine Derivatives and Their Use as Bace Inhibitors
  申请人：Broughton Barff Howard

  公开号：US20070225267A1

  公开（公告）日：2007-09-27

  The present invention provides BACE inhibitors of Formula (I); methods for their use and preparation, and intermediates useful for their preparation.

  本发明提供了化学式（I）的BACE抑制剂；以及它们的使用和制备方法，以及用于它们制备的中间体。
• Selective One-Pot Conversion of Carboxylic Acids into Alcohols
  作者：George Kokotos、Caterina Noula

  DOI：10.1021/jo9520699

  日期：1996.1.1

  Carboxylic acids are converted into alcohols by chemoselective reduction of their corresponding fluorides with sodium borohydride and dropwise addition of methanol. The method is general and mild and displays a high level of functional group compatibility. N-Protected amino and peptide alcohols, bearing varieties of protecting groups, are prepared in the same way from their corresponding amino acids and peptides

  通过用硼氢化钠化学选择性还原其相应的氟化物并滴加甲醇，可将羧酸转化为醇。该方法通用且温和，并且显示出高水平的官能团相容性。由N-保护的氨基和肽醇，带有各种保护基，可以由它们相应的氨基酸和肽以相同的方式制备，而无需消旋。