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pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide | 864245-40-9

中文名称
——
中文别名
——
英文名称
pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide
英文别名
N-(6-(2-fluoro-4-aminophenoxy)pyrimidin-4-yl)pyrrolidine-1-carboxamide;N-(6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl)pyrrolidine-1-carboxamide;4-(4-Amino-2-fluorophenoxy)-6-[(pyrrolidin-1-yl)carbonylamino]pyrimidine;N-[6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]pyrrolidine-1-carboxamide
pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide化学式
CAS
864245-40-9
化学式
C15H16FN5O2
mdl
——
分子量
317.323
InChiKey
PUMLFBDCLXGGPC-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:
    558.7±50.0 °C(Predicted)
  • 密度:
    1.430±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    93.4
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide苯乙酰氯乙腈 为溶剂, 反应 3.0h, 以45.3%的产率得到Pyrrolidine-1-carboxylic acid {6-[2-fluoro-4-(3-phenylacetylthioureido)phenoxy]pyrimidin-4-yl}amide
    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:
    参考文献:
    名称:
    WO2006/116713
    摘要:
    公开号:
  • 作为试剂:
    描述:
    Pyrrolidine-1-carboxylic acid [6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-yl]amide氯化铵铁粉 甲醇 、 hexanes 、 pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide 作用下, 以 water ethanol 为溶剂, 反应 1.0h, 以to give the desired product N-(6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl)pyrrolidine-1-carboxamide (0.240 g, 0.756 mmol, 82% yield) as a yellow solid的产率得到pyrrolidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide
    参考文献:
    名称:
    METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES
    摘要:
    选定的化合物对于预防和治疗疾病,如HGF介导的疾病非常有效。本发明包括新颖的化合物、类似物、前药和其药学上可接受的盐、制药组合物以及用于预防和治疗涉及癌症等疾病和其他疾病或情况的方法。本发明还涉及制备这些化合物的过程以及在这些过程中有用的中间体。
    公开号:
    US20120070413A1
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文献信息

  • KINASE INHIBITORS AND USES THEREOF
    申请人:Raeppel Stephane
    公开号:US20080255155A1
    公开(公告)日:2008-10-16
    This invention relates to compounds that inhibit protein tyrosine kinase activity. In particular the invention relates to compounds, compositions and methods for the inhibition of kinase activity. The invention also provides compounds, compositions and methods for treating cell proliferative diseases and conditions.
    本发明涉及抑制蛋白酪氨酸激酶活性的化合物。具体而言,本发明涉及抑制激酶活性的化合物、组合物和方法。本发明还提供用于治疗细胞增殖性疾病和病症的化合物、组合物和方法。
  • 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。]
  • Substituted amide derivatives and methods of use
    申请人:Kim Tae-Seong
    公开号:US20080312232A1
    公开(公告)日:2008-12-18
    Selected compounds are effective for prophylaxis and treatment of diseases, such as HGF mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于预防和治疗疾病,如HGF介导的疾病具有有效性。本发明涵盖了新型化合物、类似物、前药及其药学上可接受的盐、药物组合物和用于预防和治疗涉及癌症等疾病和其他疾病或状况的方法。本发明还涉及制备这些化合物的过程,以及在这些过程中有用的中间体。
  • Pyridine derivative and pyrimidine derivative
    申请人:Eisai R&D Management Co., Ltd.
    公开号:US07531532B2
    公开(公告)日:2009-05-12
    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. [R1 represents C1-6 alkyl or the like; R2 and R3 represent hydrogen; R4, R5, R6, and R7 may be the same or different and each represents hydrogen, halogen, C1-6 alkyl or the like; R8 represents hydrogen or the like; R9 represents C1-6 alkyl or the like; V1 represents oxygen or the like; V2 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、抗血管生成活性和癌症转移抑制活性。【R1代表C1-6烷基或类似物;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。】
  • SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE
    申请人:Kim Tae-Seong
    公开号:US20110118252A1
    公开(公告)日:2011-05-19
    Selected compounds are effective for prophylaxis and treatment of diseases, such as HGF mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的化合物对于预防和治疗疾病,如HGF介导的疾病具有有效性。该发明包括新型化合物、类似物、前药和其药学上可接受的盐、药物组合物以及预防和治疗癌症等疾病和其他疾病或状况的方法。本发明还涉及制备这些化合物的过程以及在这些过程中有用的中间体。
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