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methyl 4-[[4-[2-fluoro-4-[[1-[(4-fluorophenyl)aminocarbonyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxy-7-quinolyl]oxy]butyrate | 1372671-44-7

中文名称
——
中文别名
——
英文名称
methyl 4-[[4-[2-fluoro-4-[[1-[(4-fluorophenyl)aminocarbonyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxy-7-quinolyl]oxy]butyrate
英文别名
Methyl 4-[4-[2-fluoro-4-[[1-[(4-fluorophenyl)carbamoyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxyquinolin-7-yl]oxybutanoate;methyl 4-[4-[2-fluoro-4-[[1-[(4-fluorophenyl)carbamoyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxyquinolin-7-yl]oxybutanoate
methyl 4-[[4-[2-fluoro-4-[[1-[(4-fluorophenyl)aminocarbonyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxy-7-quinolyl]oxy]butyrate化学式
CAS
1372671-44-7
化学式
C32H29F2N3O7
mdl
——
分子量
605.595
InChiKey
JRXRFIBTPRAVTI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.7
  • 重原子数:
    44
  • 可旋转键数:
    13
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    125
  • 氢给体数:
    2
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    methyl 4-[[4-[2-fluoro-4-[[1-[(4-fluorophenyl)aminocarbonyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxy-7-quinolyl]oxy]butyrate盐酸羟胺 、 sodium hydroxide 作用下, 以 甲醇 为溶剂, 以290 mg的产率得到N1′-[3-fluoro-4-[[7-[4-(hydroxyamino)-4-oxobutoxy]-6-methoxy-4-quinolyl]oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
    参考文献:
    名称:
    Quinolyl-containing Hydroxamic Acid Compound and Preparation Method Thereof, and Pharmaceutical Composition Containing This Compound and Use Thereof
    摘要:
    本发明提供了一种含有喹啉基羟肟酸化合物,如式(I)所示,同时还揭示了该化合物的制备方法及其用途,以及含有该含有喹啉基羟肟酸化合物的药物组合物。这些化合物是蛋白激酶和/或组蛋白去乙酰化酶的抑制剂,可用于治疗由蛋白激酶和/或组蛋白去乙酰化酶异常活动引起的疾病,例如肿瘤等。
    公开号:
    US20140221425A1
  • 作为产物:
    描述:
    hydrobromide salt of 4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-hydroxyquinoline 在 4-二甲氨基吡啶氢气caesium carbonateN,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 甲醇N,N-二甲基甲酰胺 为溶剂, 20.0~40.0 ℃ 、206.85 kPa 条件下, 反应 19.0h, 生成 methyl 4-[[4-[2-fluoro-4-[[1-[(4-fluorophenyl)aminocarbonyl]cyclopropanecarbonyl]amino]phenoxy]-6-methoxy-7-quinolyl]oxy]butyrate
    参考文献:
    名称:
    Quinolyl-containing Hydroxamic Acid Compound and Preparation Method Thereof, and Pharmaceutical Composition Containing This Compound and Use Thereof
    摘要:
    本发明提供了一种含有喹啉基羟肟酸化合物,如式(I)所示,同时还揭示了该化合物的制备方法及其用途,以及含有该含有喹啉基羟肟酸化合物的药物组合物。这些化合物是蛋白激酶和/或组蛋白去乙酰化酶的抑制剂,可用于治疗由蛋白激酶和/或组蛋白去乙酰化酶异常活动引起的疾病,例如肿瘤等。
    公开号:
    US20140221425A1
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文献信息

  • QUINOLINYL-SUBSTITUTED CARBOXYLIC ACID COMPOUND OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, PHARMACEUTICAL COMPOSITION THEREOF, AND USE THEREOF
    申请人:Beijing Konruns Pharmaceutical Co., Ltd.
    公开号:EP3530654A1
    公开(公告)日:2019-08-28
    The present application provides a quinolyl-substituted carboxylic acid compound as shown in formula (I) or a pharmaceutically acceptable salt thereof, as well as a method for preparing the compound, a use of the compound, and a formulation containing the quinolyl-substituted carboxylic acid compound or the pharmaceutically acceptable salt thereof. This type of compounds are inhibitors for AXL and/or VEGFR2 protein kinase, and can be used to treat diseases caused by abnormality of the two protein kinases, such as, tumor, etc.;
    本申请提供了一种如式(I)所示的喹啉基取代的羧酸化合物或其药学上可接受的盐,以及该化合物的制备方法、该化合物的用途和含有该喹啉基取代的羧酸化合物或其药学上可接受的盐的制剂。这类化合物是 AXL 和/或 VEGFR2 蛋白激酶的抑制剂,可用于治疗由这两种蛋白激酶异常引起的疾病,如肿瘤等;
  • Quinolyl-substituted carboxylic acid compound or pharmaceutically acceptable salt thereof, pharmaceutical composition of the same, and use of the same
    申请人:BEIJING KONRUNS PHARMACEUTICAL CO., LTD.
    公开号:US10723701B2
    公开(公告)日:2020-07-28
    The present application provides a quinolyl-substituted carboxylic acid compound as shown in formula (I) or a pharmaceutically acceptable salt thereof, as well as a method for preparing the compound, a use of the compound, and a formulation containing the quinolyl-substituted carboxylic acid compound or the pharmaceutically acceptable salt thereof. This type of compounds are inhibitors for AXL and/or VEGFR2 protein kinase, and can be used to treat diseases caused by abnormality of the two protein kinases, such as, tumor, etc.
    本申请提供了一种如式(I)所示的喹啉基取代的羧酸化合物或其药学上可接受的盐,以及该化合物的制备方法、该化合物的用途和含有该喹啉基取代的羧酸化合物或其药学上可接受的盐的制剂。这类化合物是 AXL 和/或 VEGFR2 蛋白激酶的抑制剂,可用于治疗由这两种蛋白激酶异常引起的疾病,如肿瘤等。
  • HYDROXAMIC ACID COMPOUND CONTAINING QUINOLYL AND PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING THIS COMPOUND AND USE THEREOF
    申请人:Beijing Konruns Pharmaceutical Co., Ltd.
    公开号:EP2769976B8
    公开(公告)日:2017-12-13
  • QUINOLYL-SUBSTITUTED CARBOXYLIC ACID COMPOUND OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, PHARMACEUTICAL COMPOSITION OF THE SAME, AND USE OF THE SAME
    申请人:BEIJING KONRUNS PHARMACEUTICAL CO., LTD.
    公开号:US20190256470A1
    公开(公告)日:2019-08-22
    The present application provides a quinolyl-substituted carboxylic acid compound as shown in formula (I) or a pharmaceutically acceptable salt thereof, as well as a method for preparing the compound, a use of the compound, and a formulation containing the quinolyl-substituted carboxylic acid compound or the pharmaceutically acceptable salt thereof. This type of compounds are inhibitors for AXL and/or VEGFR2 protein kinase, and can be used to treat diseases caused by abnormality of the two protein kinases, such as, tumor, etc.;
  • US9186318B2
    申请人:——
    公开号:US9186318B2
    公开(公告)日:2015-11-17
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