(+/-)4-amino-3-phenyl-1-butene | 111462-90-9

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: (+/-)4-amino-3-phenyl-1-butene
• 英文别名: 2-Phenylbut-3-en-1-amine
• CAS: 111462-90-9
• 化学式: C₁₀H₁₃N
• mdl: MFCD00875861
• 分子量: 147.22
• InChiKey: FXIQEDXPHQLKSZ-UHFFFAOYSA-N

物化性质

• 沸点：
  62 °C(Press: 0.1 Torr)
• 密度：
  0.951±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (+/-)4-amino-3-phenyl-1-butene 在 锰 、 三甲基氯硅烷 、 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 、 nickel dibromide 作用下， 以 N,N-二甲基乙酰胺 为溶剂， 反应 18.0h， 生成 N-(3-([1,1'-biphenyl]-4-ylmethyl)-2-phenylhexyl)quinoline-2-carboxamide
  参考文献：
  名称：

  烯基胺的定向镍催化非对映选择性还原双官能化

  摘要：

  我们在此报告了使用 Ni(II) 催化剂的烯基胺与两种不同的有机卤化物（碘化物和溴化物）的分子间顺芳基烷基化和烯基烷基化。可切割的双齿喹啉酰胺在广泛的定向基团筛选后使用，以实现具有高水平区域、化学和非对映控制的烯烃双官能化。这种通用且实用的方案与α-或β-取代的末端烯烃和内部烯烃兼容，可快速获取带有两个跳跃和邻位立体中心的支链脂肪胺，这些立体中心具有高非对映选择性，否则很难合成。

  DOI：

  10.1021/acs.orglett.1c03210
• 作为产物：
  描述：

  亚苯甲基丙二酸二乙酯 在 钯 吡啶 、 盐酸 、 sodium hydroxide 、 叠氮磷酸二苯酯 、 氢气 、 三乙胺 作用下， 以 乙醚 、 二氯甲烷 、 乙酸乙酯 、 甲苯 为溶剂， 生成 (+/-)4-amino-3-phenyl-1-butene
  参考文献：
  名称：

  β-取代的苯乙胺是多巴胺β-羟化酶的基于高亲和力机理的抑制剂。

  摘要：

  DOI：

  10.1021/jm00399a002

文献信息

• Renal-selective prodrugs for control of renal sympathetic nerve activity in the treatment of hypertension
  申请人：G.D. Searle & Co.

  公开号：US20030220521A1

  公开（公告）日：2003-11-27

  Renal-selective prodrugs are described which are preferentially converted in the kidney to compounds capable of inhibiting synthesis of catecholamine-type neurotransmitters involved in renal sympathetic nerve activity. The prodrugs described herein are derived from inhibitor compounds capable of inhibiting one or more of the enzymes involved in catecholamine synthesis, such compounds being classifiable as tyrosine hydroxylase inhibitors, or as dopa-decarboxylase inhibitors, or as dopamine-&bgr;-hydroxylase inhibitors. These inhibitor compounds are linked to a chemical moiety, such as a glutamic acid derivative, by a cleavable bond which is recognized selectively by enzymes located predominantly in the kidney. The liberated inhibitor compound is then available in the kidney to inhibit one or more of the enzymes involved in catecholamine synthesis. Inhibition of renal catecholamine synthesis can suppress heightened renal nerve activity associated with sodium-retention related disorders such as hypertension. Conjugates of particular interest are glutamyl derivatives of dopamine-&bgr;-hydroxylase inhibitors, of which N-acetyl-&ggr;-glutamyl fusaric acid hydrazide (shown below) is preferred. 1

  本文描述了一种肾选择性的前药，其在肾脏中优先转化为能够抑制参与肾交感神经活动的儿茶酚型神经递质合成的化合物。本文所描述的前药来源于能够抑制儿茶酚合成中的一个或多个酶的抑制剂化合物，这些化合物可分类为酪氨酸羟化酶抑制剂，多巴脱羧酶抑制剂或多巴胺-&bgr;-羟化酶抑制剂。这些抑制剂化合物通过可被肾脏中大量存在的酶选择性识别的可裂解键与化学基团（如谷氨酸衍生物）连接。释放的抑制剂化合物然后可在肾脏中用于抑制儿茶酚合成中的一个或多个酶。抑制肾脏儿茶酚合成可抑制与钠潴留相关的疾病（如高血压）相关的增强肾脏神经活动。特别感兴趣的共轭物是多巴胺-&bgr;-羟化酶抑制剂的谷氨酰衍生物，其中N-乙酰-&ggr;-谷氨酰富萨酸肼（如下图所示）是首选。1
• NON-VIRAL DELIVERY AGENTS FROM POLYELECTROLYTES BASED ON CYCLOPROPENIUM IONS, THEIR SYNTHESES, AND USES THEREOF
  申请人：THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK

  公开号：US20210283273A1

  公开（公告）日：2021-09-16

  Non-viral gene delivery agents can be provided comprising a polyamine comprising a polymer containing a secondary amine, wherein the polyamine and a derivative of a cyclopropenium ion that are covalently attached. The non-viral gene delivery agents can be formed by a click reaction combining a polyamine polymer precursor backbone with a trisaminocyclopropenium polymer. The non-viral gene delivery agents can be used to deliver genetic material to cells in mammals or other organisms as part of gene therapy.

  非病毒基因传递剂可以包含聚合物的多胺，其中包含含有次级胺的聚合物，其中多胺和环丙烯阳离子的衍生物共价连接。非病毒基因传递剂可以通过点击反应将多胺聚合物前体骨架与三氨基环丙烯聚合物结合而形成。非病毒基因传递剂可用于作为基因治疗的一部分将遗传物质传递到哺乳动物或其他生物的细胞中。
• Renal-selective prodrugs for control of renal smpathetic nerve activity in the treatment of hypertension
  申请人：G.D. Searle & Co.

  公开号：US20040101523A1

  公开（公告）日：2004-05-27

  Renal-selective prodrugs are described which are preferentially converted in the kidney to compounds capable of inhibiting synthesis of catecholamine-type neurotransmitters involved in renal sympathetic nerve activity. The prodrugs described herein are derived from inhibitor compounds capable of inhibiting one or more of the enzymes involved in catecholamine synthesis, such compounds being classifiable as tyrosine hydroxylase inhibitors, or as dopa-decarboxylase inhibitors, or as dopamine-&bgr;-hydroxylase inhibitors. These inhibitor compounds are linked to a chemical moiety, such as a glutamic acid derivative, by a cleavable bond which is recognized selectively by enzymes located predominantly in the kidney. The liberated inhibitor compound is then available in the kidney to inhibit one or more of the enzymes involved in catecholamine synthesis. Inhibition of renal catecholamine synthesis can suppress heightened renal nerve activity associated with sodium-retention related disorders such as hypertension. Conjugates of particular interest are glutamyl derivatives of dopamine-&bgr;-hydroxylase inhibitors, of which N-acetyl-&ggr;-glutamyl fusaric acid hydrazide (shown below) is preferred. 1

  本文描述了肾脏选择性前药，这些前药被优先转化为能够抑制与肾脏交感神经活动相关的儿茶酚类神经递质合成的化合物。所述前药源自能够抑制儿茶酚类合成中涉及的一个或多个酶的抑制剂化合物，这些化合物可分类为酪氨酸羟化酶抑制剂，或多巴脱羧酶抑制剂，或是多巴胺-β-羟化酶抑制剂。这些抑制剂化合物与化学基团（例如谷氨酸衍生物）通过可被肾脏内的酶特异性识别的可切断键连接。被释放的抑制剂化合物随后可在肾脏中抑制一个或多个涉及儿茶酚类合成的酶。抑制肾脏儿茶酚类合成可以抑制与钠潴留相关的疾病（如高血压）所伴随的过度肾脏神经活动。特别感兴趣的结合物是多巴胺-β-羟化酶抑制剂的谷氨酰衍生物，其中N-乙酰-γ-谷氨酰菌核酸酸肼（如下图所示）是首选。1
• Quinolinamide-Enabled Nickel-Catalyzed Regio- and Diastereoselective γ,δ-Arylalkylation of Nonactivated Alkenes
  作者：Chao Wang、Lanlan Zhang、Lei Zhao、Yuqin Zhu

  DOI：10.1055/a-2192-7085

  日期：——

  cleavable quinolinamide directing group facilitates the stabilization of a five-membered nickelacycle, and enables the dicarbofunctionalization of nonactivated alkenes with excellently regio-, chemo-, and diastereoselectivity. The reaction with internal alkenes proceeds stereospecifically to provide valuable γ-alkyl-δ-aryl-substituted amines with two vicinal stereocenters. The scope of substrates and the

  开发了一种喹啉酰胺镍催化的高烯丙基胺与芳基碘化物和有机锌化合物的 γ,δ-芳基烷基化反应。可裂解的喹啉酰胺导向基团有利于五元镍环的稳定，并使非活化烯烃的二碳官能化具有优异的区域选择性、化学选择性和非对映选择性。与内部烯烃的反应立体定向地进行，提供具有两个邻位立体中心的有价值的γ-烷基-δ-芳基取代的胺。底物的范围和协议的实用性已得到彻底研究。
• Irreversible dopamine-Beta-hydroxylase inhibitors
  申请人：SMITHKLINE BECKMAN CORPORATION

  公开号：EP0250264A1

  公开（公告）日：1987-12-23

  Substituted β-ethenyl and β-ethynyl benzeneethanamine compounds of structrue (I) in which X is hydrogen or hydroxy; and R is ethenyl or ethynyl; are potent, irreversible inhibitors of mammalian dopamine-β-hydroxylase. Included are pharmaceutical compositions and methods for using these compounds to inhibit DH, and processes and intermediates used in preparing active compounds.

  结构式为(I)的取代 β-乙烯基和 β-乙炔基苯乙胺化合物 其中 X 为氢或羟基；R 为乙烯基或乙炔基；是哺乳动物多巴胺-β-羟化酶的强效不可逆抑制剂。包括使用这些化合物抑制 DH 的药物组合物和方法，以及用于制备活性化合物的工艺和中间体。