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ethyl 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylate | 864245-99-8

中文名称
——
中文别名
——
英文名称
ethyl 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylate
英文别名
ethyl 4-[3-fluoro-4-(phenylmethoxycarbonylamino)phenoxy]pyridine-2-carboxylate
ethyl 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylate化学式
CAS
864245-99-8
化学式
C22H19FN2O5
mdl
——
分子量
410.402
InChiKey
KKTHWBPGXXBESU-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

物化性质

  • 沸点:
    520.1±50.0 °C(Predicted)
  • 密度:
    1.315±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    30
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    86.8
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylate 在 lithium hydroxide 、 盐酸 作用下, 以 乙醇 为溶剂, 反应 1.08h, 以72%的产率得到4-(4-benzyloxycarbonylamino-3-fluorophenyl)pyridine-2-carboxylic acid
    参考文献:
    名称:
    Novel pyridine derivative and pyrimidine derivative
    摘要:
    以下化合物的分子式,其盐或前述水合物具有出色的肝细胞生长因子受体(HGFR)抑制活性,并表现出抗肿瘤活性、抑制血管生成活性和抑制癌转移活性。 [R 1 代表C 1-6 烷基或类似物;R 2 和R 3 代表氢;R 4 ,R 5 ,R 6 和R 7 可以相同也可以不同,每个代表氢、卤素、C 1-6 烷基或类似物;R 8 代表氢或类似物;R 9 代表C 1-6 烷基或类似物;V 1 代表氧或类似物;V 2 代表氧或硫;W代表—NH—或类似物;X代表—CH═、氮或类似物;Y代表氧或类似物。]
    公开号:
    US20050277652A1
  • 作为产物:
    描述:
    氯甲酸苄酯 在 palladium(II) hydroxide/carbon 氢气盐酸碳酸氢钠 作用下, 以 乙醇乙酸乙酯丙酮 为溶剂, 反应 13.5h, 以65.4%的产率得到ethyl 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylate
    参考文献:
    名称:
    Novel pyridine derivative and pyrimidine derivative
    摘要:
    以下化合物的分子式,其盐或前述水合物具有出色的肝细胞生长因子受体(HGFR)抑制活性,并表现出抗肿瘤活性、抑制血管生成活性和抑制癌转移活性。 [R 1 代表C 1-6 烷基或类似物;R 2 和R 3 代表氢;R 4 ,R 5 ,R 6 和R 7 可以相同也可以不同,每个代表氢、卤素、C 1-6 烷基或类似物;R 8 代表氢或类似物;R 9 代表C 1-6 烷基或类似物;V 1 代表氧或类似物;V 2 代表氧或硫;W代表—NH—或类似物;X代表—CH═、氮或类似物;Y代表氧或类似物。]
    公开号:
    US20050277652A1
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文献信息

  • Novel pyridine derivative and pyrimidine derivative
    申请人:Matsushima Tomohiro
    公开号:US20050277652A1
    公开(公告)日:2005-12-15
    A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity. [R 1 represents C 1-6 alkyl or the like; R 2 and R 3 represent hydrogen; R 4 , R 5 , R 6 , and R 7 may be the same or different and each represents hydrogen, halogen, C 1-6 alkyl or the like; R 8 represents hydrogen or the like; R 9 represents C 1-6 alkyl or the like; V 1 represents oxygen or the like; V 2 represents oxygen or sulfur; W represents —NH— or the like; X represents —CH═, nitrogen or the like; and Y represents oxygen or the like.]
    以下化合物的分子式,其盐或前述水合物具有出色的肝细胞生长因子受体(HGFR)抑制活性,并表现出抗肿瘤活性、抑制血管生成活性和抑制癌转移活性。 [R 1 代表C 1-6 烷基或类似物;R 2 和R 3 代表氢;R 4 ,R 5 ,R 6 和R 7 可以相同也可以不同,每个代表氢、卤素、C 1-6 烷基或类似物;R 8 代表氢或类似物;R 9 代表C 1-6 烷基或类似物;V 1 代表氧或类似物;V 2 代表氧或硫;W代表—NH—或类似物;X代表—CH═、氮或类似物;Y代表氧或类似物。]
  • PHENOXYPYRIDINE DERIVATIVE SALTS AND CRYSTALS THEREOF, AND PROCESS FOR PREPARING THE SAME
    申请人:MATSUSHIMA Tomohiro
    公开号:US20080318924A1
    公开(公告)日:2008-12-25
    The invention provides acid addition salts of the compounds represented by formula (1) or (2), or crystals thereof, and processes for preparing the same. The salts or crystals have HGFR inhibitory activity and excellent physical properties (solubility, safety, etc.) and are therefore useful as anti-tumor agents, angiogenesis inhibitors and inhibitors for metastasis for a various types of tumor.
    本发明提供了由公式(1)或(2)所代表的化合物的酸加成盐或其晶体,并提供了制备它们的方法。这些盐或晶体具有HGFR抑制活性和优异的物理性质(溶解度、安全性等),因此可用作多种类型肿瘤的抗肿瘤剂、抑制血管生成的抑制剂以及抑制转移的抑制剂。
  • Novel pyridine derivatives and pyrimidine derivatives (3)
    申请人:Matsushima Tomohiro
    公开号:US20080319188A1
    公开(公告)日:2008-12-25
    A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity. [R 1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R 2 and R 3 represent hydrogen; R 4 , R 5 , R 6 , and R 7 may be the same or different and each represents hydrogen, halogen, C 1-6 alkyl or the like; R 8 represents hydrogen or the like; R 9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen or the like.]
    以下化合物,其盐或水合物,具有优异的肝细胞生长因子受体(HGFR)抑制活性,表现出抗肿瘤活性、抑制血管生成活性和癌症转移抑制活性。[其中,R1代表3-至10-成员的非芳香族杂环基团等;R2和R3代表氢;R4、R5、R6和R7可以相同或不同,每个代表氢、卤素、C1-6烷基或类似物;R8代表氢或类似物;R9代表3-至10-成员的非芳香族杂环基团等;n代表1或2的整数;X代表-CH═,氮或类似物。]
  • Novel pyridine Derivative and Pyrimidine Derivative (1)
    申请人:Matsushima Tomohiro
    公开号:US20070270421A1
    公开(公告)日:2007-11-22
    A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity. [R 1 represents C 1-6 alkyl or the like; R 2 and R 3 represent hydrogen; R 4 , R 5 , R 6 , and R 7 may be the same or different and each represents hydrogen, halogen, C 1-6 alkyl or the like; R 8 represents hydrogen or the like; R 9 represents C 1-6 alkyl or the like; V 1 represents oxygen or the like; V 2 represents oxygen or sulfur; W represents —NH— or the like; X represents —CH═, nitrogen or the like; and Y represents oxygen or the like.]
    以下化合物的公式,其盐或水合物具有出色的肝细胞生长因子受体(HGFR)抑制活性,并表现出抗肿瘤活性,抑制血管生成活性和癌症转移抑制活性。 [其中,R1代表C1-6烷基或类似物; R2和R3代表氢; R4,R5,R6和R7可能相同或不同,每个代表氢,卤素,C1-6烷基或类似物; R8代表氢或类似物; R9代表C1-6烷基或类似物; V1代表氧或类似物; V2代表氧或硫; W代表—NH—或类似物; X代表—CH═、氮或类似物; Y代表氧或类似物。]
  • NOVEL PYRIDINE DERIVATIVES AND PYRIMIDINE DERIVATIVES (3)
    申请人:MATSUSHIMA Tomohiro
    公开号:US20100075944A1
    公开(公告)日:2010-03-25
    A compound represented by the following formula, or a salt thereof or a hydrate of the foregoing, has excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity, and cancer metastasis inhibitory activity. R 1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R 2 and R 3 represent hydrogen; R 4 , R 5 , R 6 , and R 7 may be the same or different and each represents hydrogen, halogen, C 1-6 alkyl or the like; R 8 represents hydrogen or the like; R 9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen or the like.
    以下化合物的分子式,或其盐或水合物,具有出色的肝细胞生长因子受体(HGFR)抑制活性,并表现出抗肿瘤活性、抑制血管生成活性和癌症转移抑制活性。其中,R1代表3-10个成员的非芳香杂环基团等;R2和R3代表氢;R4、R5、R6和R7可以相同也可以不同,每个代表氢、卤素、C1-6烷基或类似物;R8代表氢或类似物;R9代表3-10个成员的非芳香杂环基团等;n代表1或2的整数;X代表-CH═、氮或类似物。
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