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4-chloro-2-({[2-(trifluoromethoxy)phenyl]methyl}amino)pyrimidine-5-carbonitrile | 874822-07-8

中文名称
——
中文别名
——
英文名称
4-chloro-2-({[2-(trifluoromethoxy)phenyl]methyl}amino)pyrimidine-5-carbonitrile
英文别名
(4-chloro-5-nitrile-pyrimidin-2-yl)-(2-trifluoromethoxy-benzyl)-amine;(4-Chloro-5-cyanopyrimidin-2-yl)-(2-trifluoromethoxy-benzyl)-amine;4-chloro-2-[[2-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carbonitrile
4-chloro-2-({[2-(trifluoromethoxy)phenyl]methyl}amino)pyrimidine-5-carbonitrile化学式
CAS
874822-07-8
化学式
C13H8ClF3N4O
mdl
——
分子量
328.681
InChiKey
YQJHRISWFFJBJE-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:
    451.7±55.0 °C(Predicted)
  • 密度:
    1.50±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    70.8
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    4-chloro-2-({[2-(trifluoromethoxy)phenyl]methyl}amino)pyrimidine-5-carbonitrile 、 tert-butyl N-[4-(aminomethyl)cyclohexyl]carbamate 在 N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 以96%的产率得到(4-{[5-cyano-2-(2-trifluoromethoxy-benzylamino)-pyrimidin-4-ylamino]-methyl}-cyclohexyl)-carbamic acid tert-butyl ester
    参考文献:
    名称:
    Pyrimidine derivatives useful as inhibitors of PKC-theta
    摘要:
    披露了公式(I)的新颖化合物:其中X、Y、R1、R2和R3如本文所述定义,它们作为PKC-theta的抑制剂是有用的,因此可用于治疗通过PKC-theta活性介导或维持的多种疾病和失调,包括免疫失调和II型糖尿病。本发明还涉及包含这些化合物的药物组合物、使用这些化合物治疗各种疾病和失调的方法、制备这些化合物的方法以及在这些过程中有用的中间体。
    公开号:
    US20060025433A1
  • 作为产物:
    描述:
    2,4-二氯-5-氰基嘧啶2-(三氟甲氧基)苄胺N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 20.0h, 以54%的产率得到4-chloro-2-({[2-(trifluoromethoxy)phenyl]methyl}amino)pyrimidine-5-carbonitrile
    参考文献:
    名称:
    Pyrimidine derivatives useful as inhibitors of PKC-theta
    摘要:
    披露了公式(I)的新颖化合物:其中X、Y、R1、R2和R3如本文所述定义,它们作为PKC-theta的抑制剂是有用的,因此可用于治疗通过PKC-theta活性介导或维持的多种疾病和失调,包括免疫失调和II型糖尿病。本发明还涉及包含这些化合物的药物组合物、使用这些化合物治疗各种疾病和失调的方法、制备这些化合物的方法以及在这些过程中有用的中间体。
    公开号:
    US20060025433A1
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文献信息

  • PYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF PKC-THETA
    申请人:BARBOSA Antonio J.M.
    公开号:US20080287410A1
    公开(公告)日:2008-11-20
    Disclosed are novel compounds of formula (I): wherein X, Y, R 1 , R 2 and R 3 are as defined herein, which are useful as inhibitors of PKC-theta and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of PKC-theta, including immunological disorders and type II diabetes. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
    本发明涉及一种新型化合物,其化学式为(I):其中X,Y,R1,R2和R3的定义如本文所述,该化合物可用作PKC-theta的抑制剂,因此可用于治疗多种通过PKC-theta的活性介导或维持的疾病和疾病,包括免疫性疾病和2型糖尿病。本发明还涉及包含这些化合物的制药组合物,使用这些化合物治疗各种疾病和疾病的方法,制备这些化合物的过程以及在这些过程中有用的中间体。
  • 2,4-DIAMINOPYRIMIDINE COMPOUND
    申请人:Tanaka Akira
    公开号:US20110159019A1
    公开(公告)日:2011-06-30
    Provided is a compound which is useful as an active ingredient for a pharmaceutical having a PKCθ inhibition activity, particularly a pharmaceutical composition for inhibiting acute rejection occurring in transplantation. The present inventors have conducted extensive studies on a compound having a PKCθ inhibition activity, and as a result, they have found that a compound having a structure such as aralkyl and the like on an amino group at the 2-position and also having a structure such as an adamantylalkyl group and the like on an amino group at the 4-position of 2,4-diaminopyrimidine, or a salt thereof has an excellent PKCθ inhibition activity, thereby completing the present invention. The 2,4-diaminopyrimidine compound of the present invention can be used as a PKCθ inhibitor or an inhibitor of acute rejection occurring in transplantation.
    提供了一种化合物,可用作具有PKCθ抑制活性的药物的活性成分,尤其是用于抑制移植中发生的急性排斥的药物组合物。本发明者对具有PKCθ抑制活性的化合物进行了广泛的研究,结果发现,在2-位氨基上具有类似芳基烷基等结构,在4-位氨基上具有类似于金刚烷基烷基等结构的2,4-二氨基嘧啶化合物,或其盐具有出色的PKCθ抑制活性,从而完成了本发明。本发明的2,4-二氨基嘧啶化合物可用作PKCθ抑制剂或用于抑制移植中发生的急性排斥的抑制剂。
  • US7601714B2
    申请人:——
    公开号:US7601714B2
    公开(公告)日:2009-10-13
  • [EN] PYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF PKC-THETA<br/>[FR] DÉRIVÉS DE PYRIMIDINE UTILES COMME INHIBITEURS DE LA PKC-THÊTA
    申请人:BOEHRINGER INGELHEIM PHARMA
    公开号:WO2006014482A1
    公开(公告)日:2006-02-09
    Disclosed are novel compounds of formula: (I); wherein X, Y, R1, R2 and R3 are as defined herein, which are useful as inhibitors of PKC-theta and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of PKC-theta, including immunological disorders and type II diabetes. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
  • Pyrimidine derivatives useful as inhibitors of PKC-theta
    申请人:Barbosa J.M. Antonio
    公开号:US20060025433A1
    公开(公告)日:2006-02-02
    Disclosed are novel compounds of formula (I): wherein X, Y, R 1 , R 2 and R 3 are as defined herein, which are useful as inhibitors of PKC-theta and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of PKC-theta, including immunological disorders and type II diabetes. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
    披露了公式(I)的新颖化合物:其中X、Y、R1、R2和R3如本文所述定义,它们作为PKC-theta的抑制剂是有用的,因此可用于治疗通过PKC-theta活性介导或维持的多种疾病和失调,包括免疫失调和II型糖尿病。本发明还涉及包含这些化合物的药物组合物、使用这些化合物治疗各种疾病和失调的方法、制备这些化合物的方法以及在这些过程中有用的中间体。
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