4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(4-methyl-4H-1,2,4-triazol-3-yl)methyl]-2(1H)-quinolinone | 406162-85-4

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二芳基庚烷
• 英文名称: 4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(4-methyl-4H-1,2,4-triazol-3-yl)methyl]-2(1H)-quinolinone
• 英文别名: 4-(3-chlorophenyl)-6-[(4-chlorophenyl)-hydroxy-(4-methyl-1,2,4-triazol-3-yl)methyl]-1H-quinolin-2-one
• CAS: 406162-85-4
• 化学式: C₂₅H₁₈Cl₂N₄O₂
• 分子量: 477.35
• InChiKey: JQFVATYKOSELCB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  33
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  80
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  对氰基溴化苄 、 4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(4-methyl-4H-1,2,4-triazol-3-yl)methyl]-2(1H)-quinolinone 在 NaH 作用下， 以 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 、 N,N-二甲基甲酰胺 为溶剂， 以0.078 g (6%)的产率得到4-[[4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(4-methyl-4H-1,2,4-triazol-3-yl)methyl]-2-oxo-1(2H)-quinolinyl]methyl]-benzonitrile
  参考文献：
  名称：

  Farnesyl transferase inhibiting 6-(substituted phenyl) Methy)-quinoline and quinazoline derinazoline derivaties

  摘要：

  这项发明包括具有法尼醇转移酶抑制活性的式(I)的新化合物，其中r、s、t、Y1—Y2、R1、R2、R3、R4、R5、R6和R7具有定义的含义；它们的制备、含有它们的组合物以及它们作为药物的用途。

  公开号：

  US20040048882A1
• 作为产物：
  描述：

  [2-Chloro-4-(3-chloro-phenyl)-quinolin-6-yl]-(4-chloro-phenyl)-methanone 在 盐酸 、 正丁基锂 、 硝酸 、 sodium nitrite 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 66.75h， 生成 4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(4-methyl-4H-1,2,4-triazol-3-yl)methyl]-2(1H)-quinolinone
  参考文献：
  名称：

  4-Methyl-1,2,4-triazol-3-yl heterocycle as an alternative to the 1-methylimidazol-5-yl moiety in the Farnesyltransferase inhibitor ZARNESTRA ™

  摘要：

  Replacement of the 1-methylimidazol-5-yl moiety in the farnesyltransferase inhibitor ZARNESTRA(TM) series by a 4-methyl-1,2,4-triazol-3-yl group gave us compounds with similar structure-activity relationship profiles showing that this triazole is potentially a good surrogate to imidazole for farnesyltransferase inhibition. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.09.043

文献信息

• [EN] FARNESYL TRANSFERASE INHIBITING 6-[(SUBSTITUTED PHENYL)METHYL]-QUINOLINE AND QUINAZOLINE DERIVATIVES<br/>[FR] DERIVES DE LA QUINOLEINE ET DE LA QUINAZOLINE 6-[(PHENYLE SUBSTITUE)METHYLE] INHIBITEURS DE LA FARNESYLE TRANSFERASE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2002024683A1

  公开（公告）日：2002-03-28

  This invention comprises the novel compounds of formula (I)wherein r, s, t, Y?1-Y2, R1, R2, R3, R4, R5, R6 and R7¿ have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.

  本发明涉及具有法尼醇转移酶抑制活性的新型化合物，其化学式为(I)，其中r、s、t、Y1-Y2、R1、R2、R3、R4、R5、R6和R7具有定义的含义；以及其制备、含有它们的组合物以及它们作为药物的用途。
• Farnesyl transferase inhibiting 6-[(substituted phenyl)methyl]-quinoline and quinazoline derinazoline derivatives
  申请人：Janssen Pharmaceutica N.V.

  公开号：US07173040B2

  公开（公告）日：2007-02-06

  This invention comprises the compounds of formula (I): wherein r, s, t, Y1–Y2, R1, R2, R3, R4, R5, R6 and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.

  本发明涉及以下式子(I)的化合物： 其中r，s，t，Y1-Y2，R1，R2，R3，R4，R5，R6和R7具有定义意义，具有法尼醇转移酶抑制活性；它们的制备、含有它们的组合物以及它们作为药物的用途。
• FARNESYL TRANSFERASE INHIBITING 6- (SUBSTITUTED PHENYL)METHYL]-QUINOLINE AND QUINAZOLINE DERIVATIVES
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP1322636A1

  公开（公告）日：2003-07-02
• US7173040B2
  申请人：——

  公开号：US7173040B2

  公开（公告）日：2007-02-06
• 4-Methyl-1,2,4-triazol-3-yl heterocycle as an alternative to the 1-methylimidazol-5-yl moiety in the Farnesyltransferase inhibitor ZARNESTRA ™
  作者：Patrick Angibaud、Ashis K. Saha、Xavier Bourdrez、David W. End、Eddy Freyne、Patricia Lezouret、Geert Mannens、Laurence Mevellec、Christophe Meyer、Isabelle Pilatte、Virginie Poncelet、Bruno Roux、Gerda Smets、Jacky Van Dun、Marc Venet、Walter Wouters

  DOI：10.1016/j.bmcl.2003.09.043

  日期：2003.12

  Replacement of the 1-methylimidazol-5-yl moiety in the farnesyltransferase inhibitor ZARNESTRA(TM) series by a 4-methyl-1,2,4-triazol-3-yl group gave us compounds with similar structure-activity relationship profiles showing that this triazole is potentially a good surrogate to imidazole for farnesyltransferase inhibition. (C) 2003 Elsevier Ltd. All rights reserved.