叔-丁基(3-(苯甲基氨基)丙基)氨基甲酯 | 90914-08-2

• 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: 叔-丁基(3-(苯甲基氨基)丙基)氨基甲酯
• 英文名称: tert-butyl (3-(benzylamino)propyl)carbamate
• 英文别名: N-[N-(tert-Butyloxycarbonyl)-3-aminopropyl]benzylamine；tert-butyl N-[3-(benzylamino)propyl]carbamate
• CAS: 90914-08-2
• 化学式: C₁₅H₂₄N₂O₂
• mdl: MFCD25569757
• 分子量: 264.368
• InChiKey: MUCVPGXECWXUCZ-UHFFFAOYSA-N

物化性质

• 沸点：
  392.4±25.0 °C(Predicted)
• 密度：
  1.020±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  19
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.533
• 拓扑面积：
  50.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  叔-丁基(3-(苯甲基氨基)丙基)氨基甲酯 在 potassium tert-butylate 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以84%的产率得到2(1H)-嘧啶酮,四氢-1-(苯基甲基)—
  参考文献：
  名称：

  Inhibitory effect of novel tetrahydropyrimidine-2(1H)-thiones on melanogenesis

  摘要：

  The series of imidazoldine-2-thiones 2 and tetrahydropyrimidine-2-thiones 3 were discovered as inhibitor of alpha-MSH-induced melanin production in melanoma B16 cells. The primary bioassay showed that 1-(4-ethylbenzyl)-tetrahydropyrimidine-2(1H)-thione 3e (> 100% inhibition at 10 mu M, IC50 = 1.2 mu M) and 1-(4-tert-butylbenzyl)-tetrahydropyrimidine-2(1H)-thione 3f (> 100% inhibition at 10 mu M, IC50 = 0.76 mu M) exhibited potent inhibitory effect against alpha-MSH-induced melanin production. Compounds 3 inhibit the biosynthesis of tyrosinase without affecting its catalytic activity in melanogenesis. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.12.044
• 作为产物：
  描述：

  二碳酸二叔丁酯 在 sodium tetrahydroborate 、 magnesium sulfate 、 三乙胺 作用下， 以 氯仿 为溶剂， 反应 20.5h， 生成 叔-丁基(3-(苯甲基氨基)丙基)氨基甲酯
  参考文献：
  名称：

  Building Units for N-Backbone Cyclic Peptides. 3. Synthesis of Protected N^α-(ω-Aminoalkyl)amino Acids and N^α-(ω-Carboxyalkyl)amino Acids

  摘要：

  An improved synthesis of a family of amino acids that contain omega-aminoalkyl groups and of a new family containing omega-carboxyalkyl groups linked to the alpha-amine is described. The synthesis was performed by alkylation of suitably monoprotected alkylenediamines and protected omega-amino acids with triflates of alpha-hydroxy acid esters. The reaction proceeded with inversion of configuration yielding optically pure products. The N-alpha-(omega-aminoalkyl)amino acids and N-alpha-(omega-carboxyalkyl)amino acids were orthogonally protected to allow their incorporation into peptides by solid-phase peptide synthesis (SPPS) methodology.

  DOI：

  10.1021/jo961580e

文献信息

• [EN] EIF4E INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS D'EIF4E ET LEURS UTILISATIONS
  申请人：PIC THERAPEUTICS INC

  公开号：WO2021178488A1

  公开（公告）日：2021-09-10

  The present invention provides compounds inhibiting elF4E activity and compositions and methods of using thereof.

  本发明提供了抑制elF4E活性的化合物以及使用它们的组合物和方法。
• Synthesis of novel deuterium labelled derivatives of N-alkylated polyamines
  作者：Merja R. Häkkinen、Tuomo A. Keinänen、Alex R. Khomutov、Seppo Auriola、Janne Weisell、Leena Alhonen、Juhani Jänne、Jouko Vepsäläinen

  DOI：10.1016/j.tet.2008.10.071

  日期：2009.1

  bis-N-alkylated spermines and unsymmetrically bis-N-alkylated spermines were synthesized. Deuterium labels were introduced into the RHNCH2CH2CN intermediate either by exchanging the protons next to the nitrile group under basic conditions with D2O–EtOD mixture or/and by reducing the nitrile group to a CD2–NH2 fragment with LiAlD4.

  合成了单-N-烷基化的二氨基丙烷，亚精胺，亚精胺，对称的双-N-烷基化的亚精胺和不对称的双-N-烷基化的亚精胺的新的二，四和八氘代衍生物。通过在碱性条件下用D 2 O–EtOD混合物交换邻近腈基的质子或/和通过使用LiAlD将腈基还原为CD 2 –NH 2片段，将氘标记物引入RHNCH 2 CH 2 CN中间体中。4。
• Imides: forgotten players in the Ugi reaction. One-pot multicomponent synthesis of quinazolinones
  作者：Riccardo Mossetti、Tracey Pirali、Dèsirèe Saggiorato、Gian Cesare Tron

  DOI：10.1039/c1cc12067k

  日期：——

  Up to now, the synthesis of quinazolinones has required lengthy synthetic procedures. Here, we describe an innovative one-pot multicomponent reaction leading to highly substituted quinazolinones. We believe that this novel transformation may open the door for the generation of new and pharmacologically active quinazolinones, but, most important of all, the resurrection of the imide-Ugi scaffold paves the way for the synthesis of novel molecular architectures

  迄今为止，喹唑啉酮的合成需要冗长的合成程序。在这里，我们描述了一种创新的一锅多组分反应，可以生成高度取代的喹唑啉酮。我们相信这种新颖的转化可能为新型药理活性喹唑啉酮的产生铺平道路，但最重要的是，酰亚胺-Ugi框架的复兴为新型分子结构的合成开辟了道路。
• Synthesis of 2′-deoxyguanosine containing a<i>N</i>²-polyamine
  作者：Kanda S. Ramasamy、Farid Bakir、Brenda Baker、P. Dan Cook

  DOI：10.1002/jhet.5570300532

  日期：1993.10

  The synthesis of benzylated N2-(4,7,10,13-tetraazatridec-1-yl)-2′-deoxyguanosines 4 was accomplished by a key nucleophilic reaction of the novel unsymmetrical polyamine 2, with 3′,5′-O-(tetraisopropyldisiloxane-1,3-diyl)-2-chloro-2′-deoxyinosine (1).

  苄基化N 2-（4,7,10,13-四氮杂十三烷基-1-基）-2'-脱氧鸟苷4的合成是通过新型不对称多胺2与3'，5'- O的关键亲核反应完成的-（四异丙基二硅氧烷-1，3-二基）-2-氯-2'-脱氧肌苷（1）。
• Antisense modulation of MDM2 expression
  申请人：——

  公开号：US20030203862A1

  公开（公告）日：2003-10-30

  Compounds, compositions and methods are provided for inhibiting the expression of human mdm2. The compositions include antisense compounds targeted to nucleic acids encoding mdm2. Methods of using these oligonucleotides for inhibition of mdm2 expression and for treatment of diseases such as cancers associated with overexpression of mdm2 are provided.

  提供了用于抑制人类mdm2表达的化合物、组合物和方法。这些组合物包括针对编码mdm2的核酸的反义物质。提供了使用这些寡核苷酸抑制mdm2表达和治疗与mdm2过度表达相关的癌症等疾病的方法。