(2R,4R)-1-(tert-butoxycarbonyl)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)piperidine-2-carboxylic acid | 908294-15-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: (2R,4R)-1-(tert-butoxycarbonyl)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)piperidine-2-carboxylic acid
• 英文别名: (2R,4R)-4-[4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl]oxy-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-2-carboxylic acid
• CAS: 908294-15-5
• 化学式: C₂₆H₂₈ClFN₄O₆
• 分子量: 546.983
• InChiKey: HEXGXPZYNKDTAB-AUUYWEPGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  38
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  123
• 氢给体数：
  2
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  (2R,4R)-1-(tert-butoxycarbonyl)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)piperidine-2-carboxylic acid 、 盐酸甲胺 在 三乙胺 、 N,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下， 以 N-甲基吡咯烷酮 为溶剂， 以86.3%的产率得到tert-butyl (2R,4R)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)-2-[(methylamino)carbonyl]piperidine-1-carboxylate
  参考文献：
  名称：

  WO2006/90163

  摘要：

  公开号：
• 作为产物：
  描述：

  1-tert-butyl 2-methyl (2R,4R)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)piperidine-1,2-dicarboxylate 在 lithium hydroxide 、 水 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以84%的产率得到(2R,4R)-1-(tert-butoxycarbonyl)-4-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}oxy)piperidine-2-carboxylic acid
  参考文献：
  名称：

  WO2006/90163

  摘要：

  公开号：

文献信息

• QUINAZOLINE DERIVATIVES AS TYROSINE KINASE INHIBITORS
  申请人：Halsall Christopher Thomas

  公开号：US20110152297A1

  公开（公告）日：2011-06-23

  The invention concerns quinazoline derivatives of the Formula I, or pharmaceutically acceptable salts thereof: wherein each of R 1 , R 2 , R 3 , R 4 and m are as defined in the description; processes for their preparation; pharmaceutical compositions containing them and their use in the manufacture of a medicament for providing an anti-proliferative effect. The quinazoline derivatives of Formula I are expected to be useful in the treatment of diseases such as certain cancers mediated by erbB receptor tyrosine kinases, and, for example, EGFR tyrosine kinase.

  本发明涉及公式I的喹唑啉衍生物或其药学上可接受的盐：其中R1，R2，R3，R4和m的定义如描述中所定义；其制备方法；含有它们的制药组合物以及它们用于制造抗增殖效应药物的用途。公式I的喹唑啉衍生物预计可用于治疗某些由erbB受体酪氨酸激酶介导的癌症，例如EGFR酪氨酸激酶。
• Quinazoline derivatives as tyrosine kinase inhibitors
  申请人：Halsall Christopher Thomas

  公开号：US08735410B2

  公开（公告）日：2014-05-27

  The invention concerns quinazoline derivatives of the Formula I, or pharmaceutically acceptable salts thereof: wherein each of R1, R2, R3, R4 and m are as defined in the description; processes for their preparation; pharmaceutical compositions containing them and their use in the manufacture of a medicament for providing an anti-proliferative effect. The quinazoline derivatives of Formula I are expected to be useful in the treatment of diseases such as certain cancers mediated by erbB receptor tyrosine kinases, and, for example, EGFR tyrosine kinase.

  本发明涉及式I的喹嗪衍生物，或其药学上可接受的盐：其中R1、R2、R3、R4和m的定义如描述中所定义；它们的制备方法；含有它们的制药组合物以及它们在制造提供抗增殖效应的药物方面的应用。预计式I的喹嗪衍生物可用于治疗某些经由erbB受体酪氨酸激酶介导的癌症，例如EGFR酪氨酸激酶。
• DEUTERATED OMEGA DIPHENYLUREA RELATED COMPOUNDS AND INTERMEDIATES
  申请人：Suzhou Zelgen Biopharmaceutical Co., Ltd.

  公开号：US20140128612A1

  公开（公告）日：2014-05-08

  Methods and processes for preparation and production of deuterated ω-diphenylurea are disclosed. Especially, a kind of deuterated ω-diphenylurea compounds which can inhibit phosphokinase and the preparation method of N-(4-chloro-3-(trifluoromethyl)phenyl)-N′-(4-(2-(N-d3-methylcarbamoyl)-4-pridinyloxy)phenyl)urea are disclosed. The said deuterated diphenylurea compounds can be used for treating or preventing tumors and relative diseases.

  公开了制备和生产氘代ω-二苯基脲的方法和过程。特别是公开了一种可以抑制磷酸激酶的氘代ω-二苯基脲化合物以及N-(4-氯-3-(三氟甲基)苯基)-N′-(4-(2-(N-d3-甲基氨基)-4-吡啶氧基)苯基)脲的制备方法。所述氘代二苯基脲化合物可用于治疗或预防肿瘤及相关疾病。
• US8735410B2
  申请人：——

  公开号：US8735410B2

  公开（公告）日：2014-05-27
• WO2006/90163
  申请人：——

  公开号：——

  公开（公告）日：——