7-溴-3-丙酰吲哚 | 179473-61-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 7-溴-3-丙酰吲哚
• 英文名称: 1-(7-bromo-1H-indol-3-yl)propan-1-one
• 英文别名: 7-bromo-3-propionylindole；1-Propanone, 1-(7-broMo-1H-indol-3-yl)-
• CAS: 179473-61-1
• 化学式: C₁₁H₁₀BrNO
• 分子量: 252.11
• InChiKey: GNZMIEMXIBKHGZ-UHFFFAOYSA-N

物化性质

• 沸点：
  396.4±22.0 °C(Predicted)
• 密度：
  1.517±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  32.9
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  7-溴-3-丙酰吲哚 在 氢氧化钾 、 四(三苯基膦)钯 、 sodium carbonate 作用下， 生成 6-fluoro-3-methyl-2-(7-phenyl-3-indolyl)quinoline-4-carboxylic acid
  参考文献：
  名称：

  Heteroatom- and carbon-linked biphenyl analogs of Brequinar as immunosuppressive agents

  摘要：

  Structure-activity relationships were explored for some analogs of Brequinar having a linking atom between the 2-biphenyl substituent and the quinoline ring. Activities as inhibitors of dihydroorotate dehydrogenase and the mixed lymphocyte reaction were related to the overall shape and lipophilicity of the 2-substituent. (C) 1998 The DuPont Merck Pharmaceutical Company. Published by Elsevier Science Ltd.All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00308-4
• 作为产物：
  描述：

  7-溴吲哚 、 N,N-二甲基丙酰胺 在 三氯氧磷 作用下， 生成 7-溴-3-丙酰吲哚
  参考文献：
  名称：

  Heteroatom- and carbon-linked biphenyl analogs of Brequinar as immunosuppressive agents

  摘要：

  Structure-activity relationships were explored for some analogs of Brequinar having a linking atom between the 2-biphenyl substituent and the quinoline ring. Activities as inhibitors of dihydroorotate dehydrogenase and the mixed lymphocyte reaction were related to the overall shape and lipophilicity of the 2-substituent. (C) 1998 The DuPont Merck Pharmaceutical Company. Published by Elsevier Science Ltd.All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00308-4

文献信息

• Boron Trifluoride Etherate Promoted Regioselective 3-Acylation of Indoles with Anhydrides
  作者：Yunyun Zheng、Jiuling Li、Kai Wei

  DOI：10.3390/molecules27238281

  日期：——

  An efficient, high-yielding and scalable procedure for the regioselective 3-acylation of indoles with anhydrides promoted by boron trifluoride etherate under mild conditions was reported. This novel protocol provided a simple way to prepare 3-(benzofuran-2-yl) indole in three steps.

  报道了一种高效、高产且可扩展的程序，用于在温和条件下通过乙醚三氟化硼促进吲哚与酸酐的区域选择性 3-酰化。这种新颖的方案提供了一种分三步制备 3-(benzofuran-2-yl) 吲哚的简单方法。
• US5523408A
  申请人：——

  公开号：US5523408A

  公开（公告）日：1996-06-04
• US5578609A
  申请人：——

  公开号：US5578609A

  公开（公告）日：1996-11-26
• [EN] 2-CARBOCYCLIC AND 2-HETEROCYCLIC QUINOLINE-4-CARBOXYLIC ACIDS AND SALTS THEREOF USEFUL AS IMMUNOSUPPRESSIVE AGENTS<br/>[FR] ACIDES QUINOLINE-4-CARBOXYLIQUES 2-CARBOCYCLIQUES ET 2-HETEROCYCLIQUES ET LEURS SELS, UTILISES COMME AGENTS IMMUNODEPRESSEURS
  申请人：THE DU PONT MERCK PHARMACEUTICAL COMPANY

  公开号：WO1997006144A1

  公开（公告）日：1997-02-20

  (EN) This invention relates to 2-carbocyclic and 2-heterocyclic quinoline-4-carboxylic acid compounds, and salts thereof, to pharmaceutical compositions comprising such compounds, and to methods of using such compounds for the treatment and/or prevention of organ transplantation rejection, graft versus host disease, and chronic inflammatory diseases, including but not limited to psoriasis and rheumatoid arthritis, in a mammal.(FR) L'invention concerne des composés d'acides quinoline-4-carboxyliques 2-carbocycliques et 2-hétérocycliques ainsi que leurs sels, des composés pharmaceutiques les contenant, et des procédés d'utilisation desdits composés pour le traitement et/ou la prévention chez un mammifère du rejet du greffon, de la réaction du greffon contre l'hôte et des maladies inflammatoires chroniques, telles que, entre autres, le psoriasis et la polyarthrite rhumatoïde.
• Heteroatom- and carbon-linked biphenyl analogs of Brequinar as immunosuppressive agents
  作者：Douglas G. Batt、Joseph J. Petraitis、Susan R. Sherk、Robert A. Copeland、Randine L. Dowling、Tracy L. Taylor、Elizabeth A. Jones、Ronald L. Magolda、Bruce D. Jaffee

  DOI：10.1016/s0960-894x(98)00308-4

  日期：1998.7

  Structure-activity relationships were explored for some analogs of Brequinar having a linking atom between the 2-biphenyl substituent and the quinoline ring. Activities as inhibitors of dihydroorotate dehydrogenase and the mixed lymphocyte reaction were related to the overall shape and lipophilicity of the 2-substituent. (C) 1998 The DuPont Merck Pharmaceutical Company. Published by Elsevier Science Ltd.All rights reserved.