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ethyl 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(methylthio)pyrimidin-5-carboxylate | 1370261-93-0

中文名称
——
中文别名
——
英文名称
ethyl 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(methylthio)pyrimidin-5-carboxylate
英文别名
ethyl 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(methylthio)pyrimidine-5-carboxylate;ethyl 2-methylsulfanyl-4-[3-(triazol-2-yl)anilino]pyrimidine-5-carboxylate
ethyl 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(methylthio)pyrimidin-5-carboxylate化学式
CAS
1370261-93-0
化学式
C16H16N6O2S
mdl
——
分子量
356.408
InChiKey
FUOWFAJONCMRJG-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:
    572.8±60.0 °C(Predicted)
  • 密度:
    1.39±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    120
  • 氢给体数:
    1
  • 氢受体数:
    8

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
    • 1
    • 2
    • 3

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] SELECTIVE KINASE INHIBITORS<br/>[FR] INHIBITEURS SÉLECTIFS DE KINASES
    申请人:PORTOLA PHARM INC
    公开号:WO2013078468A1
    公开(公告)日:2013-05-30
    Provided are pyrimidine compounds for inhibiting of Syk kinase, intermediates used in making such compounds, methods for their preparation, pharmaceutical compositions thereof, methods for inhibition Syk kinase activity, and methods for treating conditions mediated at least in part by Syk kinase activity.
    提供了用于抑制Syk激酶的嘧啶化合物,用于制备这些化合物的中间体,其制备方法,药物组合物,抑制Syk激酶活性的方法,以及治疗至少部分由Syk激酶活性介导的疾病的方法。
  • SELECTIVE KINASE INHIBITORS
    申请人:PORTOLA PHARMACEUTICALS, INC.
    公开号:US20140323418A1
    公开(公告)日:2014-10-30
    Provided are pyrimidine compounds for inhibiting of Syk kinase, intermediates used in making such compounds, methods for their preparation, pharmaceutical compositions thereof, methods for inhibition Syk kinase activity, and methods for treating conditions mediated at least in part by Syk kinase activity.
    提供了用于抑制Syk激酶的嘧啶化合物,用于制备这种化合物的中间体,其制备方法,制备其制剂的制剂,抑制Syk激酶活性的方法,以及治疗至少部分由Syk激酶活性介导的病症的方法。
  • CYCLOHEXANEDIAMINE COMPOUNDS AND METHODS FOR THEIR PREPARATION
    申请人:PORTOLA PHARMACEUTICALS, INC.
    公开号:US20160009694A1
    公开(公告)日:2016-01-14
    The present invention provides processes for the preparation of cyclohexanediamine compounds of formula Ia and intermediates thereof. The compounds are useful as Syk kinase inhibitors and in various pharmaceutical compositions, and particularly useful for treating conditions mediated at least in part by Syk kinase activity.
    本发明提供了制备式Ia的环己二胺化合物及其中间体的过程。该化合物可用作Syk激酶抑制剂和各种制药组合物,并且特别适用于治疗至少部分由Syk激酶活性介导的疾病。
  • EP2782580A1
    申请人:——
    公开号:EP2782580A1
    公开(公告)日:2014-10-01
  • COMBINATION THERAPY WITH 4-(3-(2H-1,2,3-TRIAZOL-2-YL)PHENYLAMINO)-2-((1R,2S)-2-AMINOCYCLOHEXYLAMINO)PYRIMIDINE-5-CARBOXAMIDE
    申请人:Sinha Uma
    公开号:US20130244963A1
    公开(公告)日:2013-09-19
    The present invention is directed to pharmaceutical compositions and methods of using combination therapies containing a SYK inhibitor, or a pharmaceutically acceptable salt thereof, and a antineoplastic or antiinflammatory agent for the treatment of inflammatory, autoimmune and cell proliferative diseases, such as allergic reaction, transplant rejection, rheumatoid arthritis (RA), lupus, multiple sclerosis (MS) or psoriasis undesired acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), non-Hodgkin lymphoma (NHL) (including diffuse large B cell lymphoma (DLBCL)), mantle cell lymphoma, acute lymphocytic leukemia (ALL), follicular lymphoma, Burkitt's lymphoma, small Lymphocytic (SLL), Lymphoma, multiple myeloma, asthma, vasculitis, Idiopathic thrombocytopenic purpura (ITP), Heparin Induced Thrombocytopenia (HIT) and hemolytic anemia.
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