3-(trans-2-[2]pyridyl-vinyl)-aniline

• 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: 3-(trans-2-[2]pyridyl-vinyl)-aniline
• 英文别名: 3-(2-[2]pyridyl-vinyl)-aniline；3-(trans-2-[2]Pyridyl-vinyl)-anilin；3-(2-[2]Pyridyl-vinyl)-anilin；(E)-3-(2-pyridin-2-ylvinyl)phenylamine；3-[(E)-2-Pyridin-2-ylvinyl]aniline；3-[(E)-2-pyridin-2-ylethenyl]aniline
• 化学式: C₁₃H₁₂N₂
• mdl: MFCD06335539
• 分子量: 196.252
• InChiKey: WVPUKLNVCMBNMD-BQYQJAHWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  38.9
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-bromo-(4-(3-hydroxypropyl)-1H-1,2,3-triazol-1-yl)benzene 、 3-(trans-2-[2]pyridyl-vinyl)-aniline 在 tris-(dibenzylideneacetone)dipalladium(0) 、 2-二环己基磷-2,4,6-三异丙基联苯 potassium carbonate 作用下， 以 叔丁醇 为溶剂， 反应 20.0h， 以70%的产率得到3-(1-{4-[3-(2-pyridin-2-ylvinyl)phenylamino]phenyl}-1H-[1,2,3]triazol-4-yl)propan-1-ol
  参考文献：
  名称：

  Compounds for use as therapeutic agents affecting p53 expression and/or activity

  摘要：

  本发明涉及化合物(I)，其中R1和R2分别代表氢原子，(C1-C4)烷氧基，氟代(C1-C4)烷氧基，羟基，苄氧基，二(C1-C4)烷基氨基，吡啶基乙烯基，嘧啶基乙烯基，苯乙烯基，或-NHCO苯基；R3、R4和R5分别代表氢原子，(C1-C4)烷基，CONHR6基团，-CONR7R8基团，-SO2NHR6基团，或杂环烷基，可选择地被卤原子取代，-(CH2)nNR7R8基团或羟基(C1-C4)烷基；R6代表氢原子，-(CHR9)m(CH2)nNR7R8基团或(C1-C6)烷基，可选择地被羟基取代；或其药学上可接受的盐之一，用作预防、抑制或治疗患有该疾病的患者的药剂，所述疾病涉及到p53蛋白的失调。其中一些化合物是新的，也是本发明的一部分。

  公开号：

  EP2505198A1
• 作为产物：
  描述：

  (E)-2-(3-nitrostyryl)pyridine 在 tin(II) chloride dihdyrate 、 乙醇 、 sodium hydroxide 作用下， 以 水 、 乙酸乙酯 为溶剂， 反应 16.0h， 以94%的产率得到3-(trans-2-[2]pyridyl-vinyl)-aniline
  参考文献：
  名称：

  Compounds for use as therapeutic agents affecting p53 expression and/or activity

  摘要：

  本发明涉及化合物(I)，其中R1和R2分别代表氢原子，(C1-C4)烷氧基，氟代(C1-C4)烷氧基，羟基，苄氧基，二(C1-C4)烷基氨基，吡啶基乙烯基，嘧啶基乙烯基，苯乙烯基，或-NHCO苯基；R3、R4和R5分别代表氢原子，(C1-C4)烷基，CONHR6基团，-CONR7R8基团，-SO2NHR6基团，或杂环烷基，可选择地被卤原子取代，-(CH2)nNR7R8基团或羟基(C1-C4)烷基；R6代表氢原子，-(CHR9)m(CH2)nNR7R8基团或(C1-C6)烷基，可选择地被羟基取代；或其药学上可接受的盐之一，用作预防、抑制或治疗患有该疾病的患者的药剂，所述疾病涉及到p53蛋白的失调。其中一些化合物是新的，也是本发明的一部分。

  公开号：

  EP2505198A1

文献信息

• Heterobicyclic derivatives
  申请人：FUJISAWA PHARMACEUTICAL CO., LTD.

  公开号：US20020107251A1

  公开（公告）日：2002-08-08

  Heterobicyclic derivatives of the formula: 1 wherein R 1 is aryl which may have suitable substituent(s), ar(lower)alkyl which may have suitable substituent(s), halo(lower)alkyl, protected carboxy(lower)alkyl, acyl(lower)alkyl, heterocyclic group or heterocyclic(lower)alkyl which may have suitable substituent(s), R 2 is aryl which may have suitable substituent(s) or heterocyclic group, and R 3 is hydrogen, lower alkoxy or arylthio, and a pharmaceutically acceptable salt thereof which are useful as a medicament.

  公式为1的杂环双环衍生物，其中：R1是苯基，可以具有适当的取代基；芳基（较低）烷基，可以具有适当的取代基；卤代（较低）烷基；保护的羧基（较低）烷基；酰基（较低）烷基；杂环基或者可以具有适当的取代基的杂环（较低）烷基；R2是苯基，可以具有适当的取代基或者杂环基；R3是氢、较低烷氧基或者芳基硫醚。它们的药物可接受盐是有用的。
• COMPOUNDS FOR USE AS THERAPEUTIC AGENTS AFFECTING P53 EXPRESSION AND/OR ACTIVITY
  申请人：Scherrer Didier

  公开号：US20140206690A1

  公开（公告）日：2014-07-24

  The present invention relates to compound (I) wherein R1 and R2 independently represent a hydrogen atom, a (C 1 -C 4 )alkoxy group, a fluoro(C 1 -C 4 )alkoxy group, a hydroxyl group, a benzyloxy group, a di(C 1 -C 4 )alkylamino group, a pyridyl-vinyl group, a pyrimidinyl-vinyl group, a styryl group, or a —NHCOphenyl group; R3, R4 and R5 independently represent a hydrogen atom, a (C 1 -C 4 )alkyl group, a CONHR6 group, a —CONR7R8 group, a —SO 2 NHR6 group, or a heteroaryl group optionally substituted by a halogen atom, a —(CH 2 ) n NR7R8 group or a hydroxy(C 1 -C 4 )alkyl group; R6 represents a hydrogen atom, a —(CHR9) m (CH 2 ) n NR7R8 group or a (C 1- C 6 )alkyl group optionally substituted by a hydroxyl group; or anyone of its pharmaceutically acceptable salt, for use in a method for preventing, inhibiting or treating a disease in a patient suffering thereof, said disease involving a deregulated p53. Some of said compounds are new and also form part of the invention.

  本发明涉及化合物(I)，其中R1和R2分别表示氢原子，(C1-C4)烷氧基，氟(C1-C4)烷氧基，羟基，苄氧基，二(C1-C4)烷基氨基，吡啶基乙烯基，嘧啶基乙烯基，苯乙烯基或—NHCO苯基；R3，R4和R5分别表示氢原子，(C1-C4)烷基，CONHR6基，—CONR7R8基，—SO2NHR6基或杂环基，所述杂环基可选地被卤原子，—(CH2)nNR7R8基或羟基(C1-C4)烷基取代；R6表示氢原子，—(CHR9)m(CH2)nNR7R8基或(C1-C6)烷基，可选地被羟基取代；或其药学上可接受的盐之一，用于预防，抑制或治疗患有p53失调的患者的疾病的方法。其中一些化合物是新的，也是本发明的一部分。
• Pyrido[2,3-a]pyrazine derivatives as PDE-IV and TNF inhibitors
  申请人：FUJISAWA PHARMACEUTICAL CO., LTD.

  公开号：EP0920867A1

  公开（公告）日：1999-06-09

  Heterobicyclic derivatives of formula (I) wherein R1 is aryl which may have suitable substituent(s), ar(lower)alkyl which may have suitable substituent(s), halo(lower)alkyl, protected carboxy(lower)alkyl, acyl(lower)alkyl, heterocyclic group or heterocyclic(lower)alkyl which may have suitable substituent(s), R2 is aryl which may have suitable substituent(s) or heterocyclic group, and R3 is hydrogen, lower alkoxy or arylthio, and a pharmaceutically acceptable salt thereof which are useful as PDE IV and TNF inhibitors for the treatment of hepatitis in human beings and animals.

  式(I)的杂双环衍生物 其中 R1 是芳基，可具有合适的取代基；ar(低级)烷基，可具有合适的取代基；卤代(低级)烷基；受保护的羧基(低级)烷基；酰基(低级)烷基；杂环基团或杂环(低级)烷基，可具有合适的取代基、R2 是芳基（可有适当的取代基）或杂环基，R3 是氢、低级烷氧基或芳硫基，及其药学上可接受的盐，可作为 PDE IV 和 TNF 抑制剂用于治疗人类和动物的肝炎。
• Compounds for use as therapeutic agents affecting P53 expression and/or activity
  申请人：ABIVAX

  公开号：US10538485B2

  公开（公告）日：2020-01-21

  The present disclosure relates to compound (I) wherein R1 and R2 independently represent a hydrogen atom, a (C1-C4)alkoxy group, a fluoro(C1-C4)alkoxy group, a hydroxyl group, a benzyloxy group, a di(C1-C4)alkylamino group, a pyridyl-vinyl group, a pyrimidinyl-vinyl group, a styryl group, or a —NHCOphenyl group; R3, R4 and R5 independently represent a hydrogen atom, a (C1-C4)alkyl group, a CONHR6 group, a —CONR7R8 group, a —SO2NHR6 group, or a heteroaryl group optionally substituted by a halogen atom, a —(CH2)nNR7R8 group or a hydroxy(C1-C4)alkyl group; R6 represents a hydrogen atom, a —(CHR9)m(CH2)nNR7R8 group or a (C1-C6)alkyl group optionally substituted by a hydroxyl group; or anyone of its pharmaceutically acceptable salt, for use in a method for preventing, inhibiting or treating a disease in a patient suffering thereof, said disease involving a deregulated p53. Some of said compounds are new and also form part of the disclosure.

  本公开涉及化合物 (I) 其中 R1 和 R2 独立地代表氢原子、(C1-C4)烷氧基、氟(C1-C4)烷氧基、羟基、苄氧基、二(C1-C4)烷基氨基、吡啶基乙烯基、嘧啶基乙烯基、苯乙烯基或 -NHCOphenyl 基；R3、R4 和 R5 各自代表氢原子、(C1-C4)烷基、CONHR6 基团、-CONR7R8 基团、-SO2NHR6 基团或任选被卤素原子、-(CH2)nNR7R8 基团或羟基(C1-C4)烷基取代的杂芳基；R6代表氢原子、-(CHR9)m(CH2)nNR7R8基团或任选被羟基取代的(C1-C6)烷基；或其任何药学上可接受的盐，用于预防、抑制或治疗患者的疾病，所述疾病涉及p53失调。其中一些化合物是新化合物，也是本公开的一部分。
• Feist, Archiv der Pharmazie, 1902, vol. 240, p. 245
  作者：Feist

  DOI：——

  日期：——