1-(4-chlorophenyl)-3-diethylamino-propane-1-one hydrochloride | 5409-52-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(4-chlorophenyl)-3-diethylamino-propane-1-one hydrochloride
• 英文别名: β-(N,N-diethylamino)-p-chloropropiophenone hyrdochloride；1-(4-chloro-phenyl)-3-diethylamino-propan-1-one; hydrochloride；1-(4-Chlor-phenyl)-3-diaethylamino-propan-1-on; Hydrochlorid；1-Propanone, 1-(4-chlorophenyl)-3-(diethylamino)-, hydrochloride；1-(4-chlorophenyl)-3-(diethylamino)propan-1-one;hydrochloride
• CAS: 5409-52-9
• 化学式: C₁₃H₁₈ClNO*ClH
• 分子量: 276.206
• InChiKey: FQWOZIQXCXXAGL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.68
• 重原子数：
  17
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  20.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(4-chlorophenyl)-3-diethylamino-propane-1-one hydrochloride 在 正丁基锂 作用下， 以 四氢呋喃 为溶剂， 反应 49.0h， 生成 3-(4-chlorophenyl)-3-(2-diethylaminoethyl)-isochroman-1-one hydrochloride
  参考文献：
  名称：

  Isochromanone-based urotensin-II receptor agonists

  摘要：

  A series of analogues of the selective non-peptide urotensin II (UII) receptor agonist 3-(4-chlorophenyl)-3-(2-dimethylaminoethyl)-isochroman- 1-one (AC-7954, 1) was synthesized and evaluated for UII agonist activity using a functional cell-based assay. The introduction of a methyl group in the 4-position resulted in a complete loss of activity, whereas substituents in the aromatic rings were beneficial. Sterically demanding amino groups were also detrimental to the activity. Several potent agonists were identified, six compounds being equally or more potent than 1. The most potent compound in the series was the 6,7-dimethyl analogue of 1 (16, pEC(50) 6.87). The racemate of 16 was resolved into the pure enantiomers using preparative straight phase HPLC. It was shown that the potency resides in the (+)-enantiomer (pEC(50) 7.11). The synthesized compounds seem to be selective for the UII receptor as no activities were observed at the closely related SSTR3 and 5 receptors. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.01.056
• 作为产物：
  描述：

  3,4'-二氯苯丙酮 、 二乙胺 以 四氢呋喃 为溶剂， 反应 16.0h， 以75%的产率得到1-(4-chlorophenyl)-3-diethylamino-propane-1-one hydrochloride
  参考文献：
  名称：

  Isochromanone-based urotensin-II receptor agonists

  摘要：

  A series of analogues of the selective non-peptide urotensin II (UII) receptor agonist 3-(4-chlorophenyl)-3-(2-dimethylaminoethyl)-isochroman- 1-one (AC-7954, 1) was synthesized and evaluated for UII agonist activity using a functional cell-based assay. The introduction of a methyl group in the 4-position resulted in a complete loss of activity, whereas substituents in the aromatic rings were beneficial. Sterically demanding amino groups were also detrimental to the activity. Several potent agonists were identified, six compounds being equally or more potent than 1. The most potent compound in the series was the 6,7-dimethyl analogue of 1 (16, pEC(50) 6.87). The racemate of 16 was resolved into the pure enantiomers using preparative straight phase HPLC. It was shown that the potency resides in the (+)-enantiomer (pEC(50) 7.11). The synthesized compounds seem to be selective for the UII receptor as no activities were observed at the closely related SSTR3 and 5 receptors. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.01.056

文献信息

• Synthesis of β-amino ketones derived from aminobenzoic acids
  作者：G. A. Gevorgyan、G. Yu. Khachvankyan、A. G. Agababyan、N. Z. Akopyan、G. A. Panosyan、M. G. Malakyan

  DOI：10.1134/s1070363217020311

  日期：2017.2

  Alkylation of aminobenzoic acids and their derivatives with 3-diethylamino-1-arylpropan-1-one hydrochlorides gave the corresponding β-aminopropiophenones some of which were tested for antioxidant activity.

  用3-二乙基氨基-1-芳基丙烷-1-酮盐酸盐将氨基苯甲酸及其衍生物烷基化，得到相应的β-氨基苯乙酮，其中一些已被测试抗氧化活性。
• 4-(β-Arylvinyl)-3-(β-arylvinylketo)-1-ethyl-4-piperidinols and Related Compounds:  A Novel Class of Cytotoxic and Anticancer Agents
  作者：Jonathan R. Dimmock、Sarvesh C. Vashishtha、J. Wilson Quail、Uma Pugazhenthi、Zbigniew Zimpel、Athena M. Sudom、Theresa M. Allen、Grace Y. Kao、Jan Balzarini、Erik De Clercq

  DOI：10.1021/jm9801455

  日期：1998.10.1

  tumors. In general, Mannich bases containing olefinic bonds were more cytotoxic than the analogues without this functional group, while the piperidines 9 and 11 were more potent than the acyclic analogues 1 and 4, respectively. Correlations were noted between various physicochemical constants in the aryl rings and cytotoxicity. Compound 9d displayed promising in vivo activity against colon cancers. This

  完成了一系列1-芳基-5-二乙基氨基-1-戊-3-酮盐酸盐1和1-芳基-3-二乙基氨基-1-丙烷盐酸盐4的合成。尝试制备相应的双（5-芳基-3-氧代-4-戊烯基）乙胺盐酸盐2和双（3-芳基-3-氧代丙基）乙胺盐酸盐5导致形成一系列4-（β-芳基乙烯基） ）-3-（β-芳基乙烯基酮）-1-乙基-4-哌啶醇盐酸盐9和4-芳基-3-芳基酮-1-乙基-4-哌啶醇盐酸盐11盐10和12。这些化合物的结构通过1 H NMR光谱确定，并通过代表性分子的X射线晶体学证实。大多数化合物对鼠P388和L1210细胞以及人类肿瘤均表现出明显的细胞毒性。通常，含有烯键的曼尼希碱比没有该官能团的类似物具有更高的细胞毒性，而哌啶9和11分别比无环类似物1和4更有效。注意到芳基环中各种物理化学常数与细胞毒性之间的相关性。化合物9d显示出抗结肠癌的有希望的体内活性。这项研究表明，哌啶9和11构成了新型的细胞毒剂。化合物9
• Pandeya; Sowmyalakshmi; Panda, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2003, vol. 42, # 10, p. 2657 - 2661
  作者：Pandeya、Sowmyalakshmi、Panda、Pandeya、Stables

  DOI：——

  日期：——
• Synthesis and Anti-MAO Activity of Alkylation Products of 2-Aminobenzamide, 2-Amino-1-(4-nitrophenyl)propane-1,3-diol, and Some Amino Acids with Mono- and Bis-β-aminoketones
  作者：N. Z. Akopyan、A. G. Agababyan、Z. A. Ovasyan、A. U. Isakhanyan、A. S. Grigoryan、K. G. Navoyan、G. V. Gasparyan、H. A. Panosyan

  DOI：10.1134/s1070363222060019

  日期：2022.6
• Isochromanone-based urotensin-II receptor agonists
  作者：Fredrik Lehmann、Erika A. Currier、Roger Olsson、Uli Hacksell、Kristina Luthman

  DOI：10.1016/j.bmc.2005.01.056

  日期：2005.4

  A series of analogues of the selective non-peptide urotensin II (UII) receptor agonist 3-(4-chlorophenyl)-3-(2-dimethylaminoethyl)-isochroman- 1-one (AC-7954, 1) was synthesized and evaluated for UII agonist activity using a functional cell-based assay. The introduction of a methyl group in the 4-position resulted in a complete loss of activity, whereas substituents in the aromatic rings were beneficial. Sterically demanding amino groups were also detrimental to the activity. Several potent agonists were identified, six compounds being equally or more potent than 1. The most potent compound in the series was the 6,7-dimethyl analogue of 1 (16, pEC(50) 6.87). The racemate of 16 was resolved into the pure enantiomers using preparative straight phase HPLC. It was shown that the potency resides in the (+)-enantiomer (pEC(50) 7.11). The synthesized compounds seem to be selective for the UII receptor as no activities were observed at the closely related SSTR3 and 5 receptors. (c) 2005 Elsevier Ltd. All rights reserved.