4-(3-trifluoromethyl-phenyl)-1H-indole | 442562-70-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-(3-trifluoromethyl-phenyl)-1H-indole
• 英文别名: 4-[3-(trifluoromethyl)phenyl]-1H-indole
• CAS: 442562-70-1
• 化学式: C₁₅H₁₀F₃N
• 分子量: 261.246
• InChiKey: BEERMOVIYPWSSZ-UHFFFAOYSA-N

物化性质

• 沸点：
  393.6±42.0 °C(Predicted)
• 密度：
  1.301±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  15.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(3-trifluoromethyl-phenyl)-1H-indole 在 sodium hydroxide 、 sodium cyanoborohydride 、 溶剂黄146 作用下， 以 乙醇 为溶剂， 生成 Sodium;6-fluoro-3-methyl-2-[4-[3-(trifluoromethyl)phenyl]-2,3-dihydroindol-1-yl]quinoline-4-carboxylate
  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：

  在 铁粉 、 溶剂黄146 作用下， 以 乙醇 为溶剂， 生成 4-(3-trifluoromethyl-phenyl)-1H-indole
  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
• 作为试剂：
  描述：

  4-溴吲哚 、 3-(三氟甲基)苯硼酸 、 sodium hydroxide 在 钯 氮气 、 水 、 乙酸乙酯 、 Brine 、 Sodium sulfate-III 、 crude product 、 silica gel 、 hexanes—EtOAc 、 4-(3-trifluoromethyl-phenyl)-1H-indole 作用下， 以 四氢呋喃 、 乙酸乙酯 为溶剂， 反应 16.0h， 以to provide 3.55 g (89%) of the product 4-(3-trifluoromethyl-phenyl)-1H-indole的产率得到N-(3-trifluoromethylphenyl)indole
  参考文献：
  名称：

  4-aryl substituted indolinones

  摘要：

  本发明涉及4-芳基吲哚酮及其制药组合物，能够调节蛋白激酶信号转导，以调节、调控和/或抑制异常细胞增殖。本发明还涉及治疗蛋白激酶相关疾病的方法。

  公开号：

  US06861418B2

文献信息

• 4-Aryl substituted indolinones
  申请人：Sugen, Inc.

  公开号：US20040157909A1

  公开（公告）日：2004-08-12

  The present invention relates to 4-arylindolinones, as well as pharmaceutical compositions thereof, capable of modulating protein kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation. The present invention also relates to methods for treating protein kinase related disorders.

  本发明涉及4-芳基吲哚酮，以及其制药组合物，能够调节蛋白激酶信号传导，以调节、调节和/或抑制异常细胞增殖。本发明还涉及用于治疗蛋白激酶相关疾病的方法。
• 4-(HETERO)ARYL SUBSTITUTED INDOLINONES
  申请人：Sugen, Inc.

  公开号：EP1349852A2

  公开（公告）日：2003-10-08
• US6677368B2
  申请人：——

  公开号：US6677368B2

  公开（公告）日：2004-01-13
• US6861418B2
  申请人：——

  公开号：US6861418B2

  公开（公告）日：2005-03-01
• [EN] 4-ARYL SUBSTITUTED INDOLINONES<br/>[FR] INDOLINONES 4-ARYL SUBSTITUEES
  申请人：CUI JINGRONG

  公开号：WO2002055517A2

  公开（公告）日：2002-07-18

  The present invention relates to 4-arylindolinones of formula (I), as well as pharmaceutical compositions thereof, capable of modulating protein kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation. The present invention relates to methods for treating protein kinase related disorders. Formula (I) wherein: R1 is an optionally substituted aryl or heteroaryl substituent, R2-R5 are as in claim 1.