4-Propyl-2-phenylmorpholin | 21532-11-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 恶嗪烷类
• 英文名称: 4-Propyl-2-phenylmorpholin
• 英文别名: 2-phenyl-4-propyl-morpholine；2-Phenyl-4-propyl-tetrahydro-1,4-oxazine；2-phenyl-4-propylmorpholine
• CAS: 21532-11-6
• 化学式: C₁₃H₁₉NO
• 分子量: 205.3
• InChiKey: VYAMLADJSHKTKB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  在 硼烷四氢呋喃络合物 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 生成 4-Propyl-2-phenylmorpholin
  参考文献：
  名称：

  Design and synthesis of a functionally selective D3 agonist and its in vivo delivery via the intranasal route

  摘要：

  This paper reports the synthesis and biological activity of a novel series of aryl-morpholine dopamine receptor agonists. Several compounds show high levels of functional selectivity for the D3 over the D2 dopamine receptor. Compound 26 has > 1000-fold functional selectivity and has been successfully progressed in vivo using an intranasal delivery route. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.10.059

文献信息

• Eine neue Methode zur Darstellung von 2,4‐disubstitutierten Morpholinen
  作者：Kitka Yordanova、Vassilii Shvedov、Damian Dantchev

  DOI：10.1002/cber.19821150726

  日期：1982.7

  Bei der reduktiven Aminierung von ω-Acetoxyacetophenonen (Acyloinestern) 1 mit sekundären Aminoethanolen 3 und Ameisensäure nach der Leuckart-Wallach-Reaktion werden 2-(Aryl),4-disubstituierte Morpholine 5 gewonnen. Die Zwischenstufen der Reaktion werden diskutiert. Die ω-Halogenacetophenone reagieren analog.

  在ω-acetoxyacetophenones（偶姻酯）的还原胺化1与仲氨基乙醇3和根据洛伊卡特-沃勒克反应，2-（芳基）甲酸，4-二取代的吗啉是5获得。讨论了反应的中间阶段。ω-卤代苯乙酮的反应类似。
• Probe compound for detecting and isolating enzymes and means and methods using the same
  申请人：Helmholtz-Zentrum für Infektionsforschung GmbH

  公开号：EP2230312A1

  公开（公告）日：2010-09-22

  The present invention relates to a probe compound that can comprise any substrate or metabolite of an enzymatic reaction in addition to an indicator component, such as, for example, a fluorescence dye, or the like. Moreover, the present invention relates to means for detecting enzymes in form of an array, which comprises any number of probe compounds of the invention which each comprise a different metabolite of interconnected metabolites representing the central pathways in all forms of life. Moreover, the present invention relates to a method for detecting enzymes involving the application of cell extracts or the like to the array of the invention which leads to reproducible enzymatic reactions with the substrates. These specific enzymatic reactions trigger the indicator (e.g. a fluorescence signal) and bind the enzymes to the respective cognate substrates. Moreover, the invention relates to means for isolating enzymes in form of nanoparticles coated with the probe compound of the invention. The immobilisation of the cognate substrates or metabolites on the surface of nanoparticles by means of the probe compounds allows capturing and isolating the respective enzyme, e.g. for subsequent sequencing.

  本发明涉及一种探针化合物，它可以包括酶反应的任何底物或代谢物，此外还包括指示成分，例如荧光染料或类似物。此外，本发明还涉及以阵列形式检测酶的方法，该阵列由任意数量的本发明探针化合物组成，每种探针化合物由代表所有生命形式中中心途径的相互关联的代谢物中的不同代谢物组成。此外，本发明还涉及一种检测酶的方法，该方法涉及将细胞提取物或类似物应用于本发明的阵列，从而导致与底物发生可重复的酶反应。这些特定的酶反应会触发指示剂（如荧光信号），并将酶与各自的同源底物结合。此外，本发明还涉及以涂覆有本发明探针化合物的纳米颗粒形式分离酶的方法。通过探针化合物将同源底物或代谢物固定在纳米颗粒表面，可以捕获和分离相应的酶，例如用于后续测序。
• Process for the preparation of arylethylamines by amination of arylolefins
  申请人：——

  公开号：US20010047097A1

  公开（公告）日：2001-11-29

  The invention relates to a process for the preparation of 2-arylethylamine derivates having an alkyl substituent in the 1-position, of the formula (I) aryl-CHR 1 —CR 2 (NR 3 R 4 )—(CHR 5 R 6 ) n —CHR 7 R 8 (I) by reaction of aromatic olefins of the general formulae (Ila-c) aryl-CHR 1 —CHR 2 —(CR 5 R 6 ) a —CR 5 ═CR 6 —(CR 5 R 6 ) b CHR 7 R 8 (IIa) aryl-CHR 1 —CR 2 ═CR 5 —(CR 5 R 6 ) c —CHR 7 R 8 (IIb) aryl-CHR 1 —CHR 2 —(CR 5 CR 6 ) c —CR 5 ═CR 7 CR 8 (IIc) with amines of the general formula (III) R 3 R 4 NH in the presence of a base.

  本发明涉及一种 2-芳基乙胺衍生物的制备方法，该衍生物在 1 位具有烷基取代基，其式为 (I) 芳基-CHR 1 -CR 2 (NR 3 R 4 )-(CHR 5 R 6 ) n -CHR 7 R 8 (I) 通过与通式（Ila-c）的芳香族烯烃反应 芳基-CHR 1 -CHR 2 -(CR 5 R 6 ) a -CR 5 ═CR 6 -(CR 5 R 6 ) b CHR 7 R 8 (IIa) 芳基-CHR 1 -CR 2 ═CR 5 -(CR 5 R 6 ) c -CHR 7 R 8 (IIb) 芳基-CHR 1 -CHR 2 -(CR 5 CR 6 ) c -CR 5 ═CR 7 CR 8 (IIc) 与通式（III）的胺 R 3 R 4 NH 在有碱存在的情况下。
• YORDANOVA, K.;SHVEDOV, V.;DANTCHEV, D., CHEM. BER., 1982, 115, N 7, 2635-2642
  作者：YORDANOVA, K.、SHVEDOV, V.、DANTCHEV, D.

  DOI：——

  日期：——
• Design and synthesis of a functionally selective D3 agonist and its in vivo delivery via the intranasal route
  作者：Julian Blagg、Charlotte M.N. Allerton、David V.J. Batchelor、Andrew D. Baxter、Denise J. Burring、Christopher L. Carr、Andrew S. Cook、Carly L. Nichols、Joanne Phipps、Vivienne G. Sanderson、Hugh Verrier、Stephen Wong

  DOI：10.1016/j.bmcl.2007.10.059

  日期：2007.12

  This paper reports the synthesis and biological activity of a novel series of aryl-morpholine dopamine receptor agonists. Several compounds show high levels of functional selectivity for the D3 over the D2 dopamine receptor. Compound 26 has > 1000-fold functional selectivity and has been successfully progressed in vivo using an intranasal delivery route. (c) 2007 Elsevier Ltd. All rights reserved.