(S)-2-苄基-2-n-boc氨基乙基硫醇 | 141437-85-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: (S)-2-苄基-2-n-boc氨基乙基硫醇
• 中文别名: 1-(苄基)苯并咪唑
• 英文名称: (S)-tert-butyl (1-mercapto-3-phenylpropan-2-yl)carbamate
• 英文别名: tert-butyl N-[(2S)-1-phenyl-3-sulfanylpropan-2-yl]carbamate
• CAS: 141437-85-6
• 化学式: C₁₄H₂₁NO₂S
• 分子量: 267.392
• InChiKey: PYBYEBRVJRDWPB-LBPRGKRZSA-N

物化性质

• 熔点：
  108-110℃
• 沸点：
  397.0±42.0 °C(Predicted)
• 密度：
  1.077±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  39.3
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2930909090

反应信息

• 作为反应物：
  描述：

  (S)-2-苄基-2-n-boc氨基乙基硫醇 在 碘 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 2.5h， 生成 (S)-1-((S)-2-Amino-3-phenyl-propyldisulfanylmethyl)-2-phenyl-ethylamine; compound with trifluoro-acetic acid
  参考文献：
  名称：

  Potent and systemically active aminopeptidase N inhibitors designed from active-site investigation

  摘要：

  Derivatives of amino acids bearing various zinc-coordinating moieties (SH, COOH, CONHOH, and PO3H2) were synthesized and tested for their ability to inhibit aminopeptidase N (APN). Among them, beta-amino thiols were found to be the most efficient with IC50's in the 11-50 nM range. These results suggest that the S1 subsite of APN is a deep but not very large hydrophobic pocket, optimally fitting side chains of moderate bulk endowed with some degree of freedom. The iv administration of the inhibitors, alone, did not induce antinociceptive responses on the hot plate test in mice. However, in presence of 10 mg/kg acetorphan, a prodrug of the neutral endopeptidase inhibitor thiorphan, these compounds gave a large increase in the jump latency time with ED50's of 2 and 2.4 mg/kg for the disulfides of methioninethiol [H2NCH(CH2CH2SCH3)CH2S]2 and S-oxomethioninethiol [H2NCH(CH2CH2S(O)CH3)CH2S]2, respectively. These results show that the disulfide forms of beta-amino thiols are efficient prodrugs of aminopeptidase N inhibitors capable of crossing the blood-brain barrier.

  DOI：

  10.1021/jm00085a013
• 作为产物：
  描述：

  (S)-N-叔丁氧羰基-alpha-(碘甲基)苯乙胺 在 sodium trithiocarbonate 、 盐酸 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 1.5h， 以70%的产率得到(S)-2-苄基-2-n-boc氨基乙基硫醇
  参考文献：
  名称：

  使用三硫代碳酸钠从相应的碘化物中简单制备 N 保护的手性 β-氨基烷基硫醇

  摘要：

  摘要报道了一种制备 N-保护的氨基烷基硫醇的简单方案，该方案采用三硫代碳酸钠 (Na2CS3) 与 N-保护的氨基烷基碘的反应。Na2CS3 易于制备，该协议避免使用强碱和多个步骤。制备的所有硫醇化合物均作为对映体纯样品获得，并使用 NMR 和质谱法进行表征。图形概要

  DOI：

  10.1080/00397911.2011.595522

文献信息

• Mild and selective silicon-mediated access to enantioenriched 1,2-mercaptoamines and β-amino arylchalcogenides
  作者：Damiano Tanini、Cosimo Borgogni、Antonella Capperucci

  DOI：10.1039/c9nj00657e

  日期：——

  Metal-free ring opening reactions of activated and unactivated aziridines with different silyl chalcogenides are described. Judicious tuning of the reaction conditions enables the synthesis of chiral enantioenriched N-Ts and N-Boc 1,2-mercaptoamines in good yields from the corresponding aziridines and bis(trimethylsilyl)sulfide. N-Protected and N-H unactivated aziridines are efficiently converted into

  描述了活化的和未活化的氮丙啶与不同的甲硅烷基硫属元素化物的无金属开环反应。通过适当调节反应条件，可以从相应的氮丙啶和双（三甲基甲硅烷基）硫化物以高收率合成手性对映体富集的N -Ts和N -Boc 1,2-巯基胺。用合适的芳族硫属元素硅烷处理后，N-保护的和N -H未活化的氮丙啶被有效地转化为相应的β-芳族硫属元素胺。硅介导的开环反应以优异的区域选择性和立体特异性进行，从而可以使用各种各样的合成和生物学上有价值的对映体富集的硫属元素胺。
• Mixed-inhibitor-prodrug as a new approach toward systemically active inhibitors of enkephalin-degrading enzymes
  作者：Marie Claude Fournie-Zaluski、Pascal Coric、Serge Turcaud、Evelyne Lucas、Florence Noble、Raphael Maldonado、Bernard P. Roques

  DOI：10.1021/jm00091a016

  日期：1992.6

  In order to evaluate the possible advantages of potentiating the effects of the endogenous enkephalins, to obtain analgesia without the serious drawbacks of morphine, it was essential to design systemically active compounds which inhibit the two metabolizing enzymes, aminopeptidase N (APN) and neutral endopeptidase 24.11 (NEP). A new concept combining the idea of "prodrug" and "mixed inhibitor" was therefore developed. Given the high efficiency of beta-mercaptoalkylamines as APN inhibitors and of N-(mercaptoacyl) amino acids as NEP inhibitors, compounds associating these molecules through disulfide or thioester bonds, which are known to increase lipophilicity and to favor passage across the blood-brain barrier, have been synthesized. An HPLC study indicated that the disulfide bridge was resistant to serum enzymes but was cleaved by brain membrane homogenates, suggesting that the active inhibitors were released in the central nervous system. The validity of the approach was verified by the efficient antinociceptive responses obtained in the hot plate test in mice after iv administration of disulfide-containing inhibitors (ED50s of from 4 to 26 mg/kg on the jump latency time). The analgesic potencies of the "mixed inhibitor-prodrug" RB 101 [H2NCH(CH2CH2SCH3)CH2SSCH2CH(CH2Ph)CONHCH(CH2Ph)COOCH2Ph] after iv administration were three times greater than those of a similar combined dose of its two constitutive moieties. The separation of the two diastereoisomers constituting RB 101 showed that the analgesia has a stereochemical dependence, the (S,S,S)-isomer being more active than the (S,R,S)-isomer. Furthermore, in the tail flick test in the rat, RB 101 gave 38% analgesia at a dose of 80 mg/kg. Due to its high efficiency and its longer pharmacological effect, RB 101 was selected for a complete study of its analgesic properties.