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2-amino-N-hydroxypyrimidine-5-carboximidamide | 930121-81-6

中文名称
——
中文别名
——
英文名称
2-amino-N-hydroxypyrimidine-5-carboximidamide
英文别名
2-amino-N-hydroxy-pyrimidine-5-carboxamidine;2-amino-N'-hydroxypyrimidine-5-carboximidamide
2-amino-N-hydroxypyrimidine-5-carboximidamide化学式
CAS
930121-81-6
化学式
C5H7N5O
mdl
——
分子量
153.143
InChiKey
ODBDZDOAMMXVMQ-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):
    -1
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    110
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    [EN] COMPOUNDS AND METHODS
    [FR] COMPOSÉS ET PROCÉDÉS
    摘要:
    公开号:
    WO2013066839A3
  • 作为产物:
    描述:
    2-氨基嘧啶-5-腈盐酸羟胺potassium carbonate 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以72%的产率得到2-amino-N-hydroxypyrimidine-5-carboximidamide
    参考文献:
    名称:
    Novel compounds as metabotropic glutamate receptor antagonists
    摘要:
    本发明涉及具有以下结构的化合物(I)其中A、E、G、J、L、M、R1、R2和R3如规范和索赔中所定义。该发明还涉及含有这种化合物的药物组合物以及制备这些化合物和组合物的方法。这些化合物是代谢型谷氨酸受体拮抗剂,可用于治疗各种中枢神经系统疾病。
    公开号:
    US20070072879A1
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文献信息

  • Novel compounds as metabotropic glutamate receptor antagonists
    申请人:McArthur Gatti Silvia
    公开号:US20070072879A1
    公开(公告)日:2007-03-29
    The present invention relates to compounds of formula (I) wherein A, E G, J, L, M, R 1 , R 2 , and R 3 are as defined in the specification and claims. The invention also relates to pharmaceutical compositions containing such compounds and methods for preparing the compounds and compositions. The compounds are metabotropic glutamate receptor antagonists and are useful for the treatment of a variety of CNS disorders.
    本发明涉及具有以下结构的化合物(I)其中A、E、G、J、L、M、R1、R2和R3如规范和索赔中所定义。该发明还涉及含有这种化合物的药物组合物以及制备这些化合物和组合物的方法。这些化合物是代谢型谷氨酸受体拮抗剂,可用于治疗各种中枢神经系统疾病。
  • Pyridine and pyrimidine derivatives as mGIuR2 antagonists
    申请人:McArthur Silvia Gatti
    公开号:US20070232583A1
    公开(公告)日:2007-10-04
    The present invention relates to compounds of formula (I), a process for the manufacture thereof, pharmaceutical compositions containing them, and their use for treating CNS disorders: wherein A, B, X, Y, R 1 , R 2 , R 3 and R 4 are as defined in the description and claims.
    本发明涉及公式(I)的化合物,其制造过程,包含它们的药物组合物以及它们用于治疗中枢神经系统疾病的用途: 其中A,B,X,Y,R1,R2,R3和R4如描述和要求中所定义。
  • PYRIDINE AND PYRIMIDINE DERIVATIVES AS MGLUR 2 ANTAGONISTS
    申请人:Gatti McArthur Silvia
    公开号:US20090318474A1
    公开(公告)日:2009-12-24
    The present invention relates to compounds of formula (I), a process for the manufacture thereof, pharmaceutical compositions containing them, and their use for treating CNS disorders: wherein A, B, X, Y, R 1 , R 2 , R 3 and R 4 are as defined in the description and claims.
    本发明涉及化合物的公式(I),其制造过程,包含它们的药物组合物,以及用于治疗中枢神经系统疾病的方法:其中A、B、X、Y、R1、R2、R3和R4如描述和权利要求所定义。
  • Compounds as metabotropic glutamate receptor antagonists
    申请人:Hoffmann-La Roche Inc.
    公开号:US07504404B2
    公开(公告)日:2009-03-17
    The present invention relates to compounds of formula (I) wherein A, E G, J, L, M, R1, R2, and R3 are as defined in the specification and claims. The invention also relates to pharmaceutical compositions containing such compounds and methods for preparing the compounds and compositions. The compounds are metabotropic glutamate receptor antagonists and are useful for the treatment of a variety of CNS disorders.
    本发明涉及式(I)的化合物,其中A、E、G、J、L、M、R1、R2和R3如说明书和权利要求所定义。本发明还涉及含有这种化合物的制药组合物和制备这种化合物及组合物的方法。这些化合物是代谢型谷氨酸受体拮抗剂,可用于治疗多种中枢神经系统疾病。
  • SUBSTITUTED PYRAZOLO [1,5-A] PYRIMIDINES AS METABOTROPIC GLUTAMATE ANTAGONISTS
    申请人:Gatti McArthur Silvia
    公开号:US20120041002A1
    公开(公告)日:2012-02-16
    The present invention relates to compounds of formula (I) wherein A, E G, J, L, M, R 1 , R 2 , and R 3 are as defined in the specification and claims. The invention also relates to pharmaceutical compositions containing such compounds and methods for preparing the compounds and compositions. The compounds are metabotropic glutamate receptor antagonists and are useful for the treatment of a variety of CNS disorders.
    本发明涉及式(I)的化合物,其中A,E,G,J,L,M,R1,R2和R3如规范和权利要求中所定义。该发明还涉及含有这种化合物的药物组合物以及制备这种化合物和组合物的方法。这些化合物是代谢型谷氨酸受体拮抗剂,可用于治疗多种中枢神经系统疾病。
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