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N1,N1-dimethyl-N2-[4-cyanopyrazol-5-yl]formamidine | 78972-81-3

中文名称
——
中文别名
——
英文名称
N1,N1-dimethyl-N2-[4-cyanopyrazol-5-yl]formamidine
英文别名
5-<(Dimethylamino)methylenamino>-4-pyrazolcarbonitril;1H-4-cyano-5-[(N,N-dimethylaminomethylene)amino]pyrazole;4-Cyano-5-dimethylaminomethyleneaminopyrazole;N'-(4-cyano-1H-pyrazol-5-yl)-N,N-dimethylmethanimidamide
N<sup>1</sup>,N<sup>1</sup>-dimethyl-N<sup>2</sup>-[4-cyanopyrazol-5-yl]formamidine化学式
CAS
78972-81-3
化学式
C7H9N5
mdl
MFCD00140669
分子量
163.182
InChiKey
KHSMXXWEJUQZOF-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):
    -0.1
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.285
  • 拓扑面积:
    68.1
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

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文献信息

  • Microwave-assisted synthesis of some novel fluorinated pyrazolo[3,4-d]pyrimidine derivatives containing 1,3,4-thiadiazole as potential antitumor agents
    作者:Xin Jian Song、Yu Shao、Xing Gao Dong
    DOI:10.1016/j.cclet.2011.05.012
    日期:2011.9
    A facile microwave-assisted procedure for synthesis of novel fluorinated pyrazolo[3,4-d]pyrimidine derivatives containing 1,3,4-thiadiazole is described. This protocol presented such advantages as short reaction time, high yields, simple purification and environmentally benign procedures. Their antitumor activities were evaluated against HL-60 by an MTT assay. The preliminary results indicated that
    描述了一种简便的微波辅助方法,用于合成含有1,3,4-噻二唑的新型吡唑并[3,4-d]嘧啶生物。该方案具有反应时间短,产率高,纯化简单和对环境无害的优点。通过MTT试验评估了它们对HL-60的抗肿瘤活性。初步结果表明,某些标题化合物比阿霉素(DOX)表现出更强的抗肿瘤抑制活性。
  • Tisler, Miha; Stanovnik, Branko; Zrimsek, Zdenka, Heterocycles, 1982, vol. 17, p. 405 - 411
    作者:Tisler, Miha、Stanovnik, Branko、Zrimsek, Zdenka
    DOI:——
    日期:——
  • A New Synthesis of Amino Substituted Azolo[1,3,5]triazines via Reaction of N1,N1-Dimethyl-N2-azolylformamidines with Cyanamide
    作者:Anton V. Dolzhenko、Dmitrii V. Kalinin、Svetlana A. Kalinina
    DOI:10.3987/com-12-12601
    日期:——
    The amino substituted triazine ring was annelated to aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of azolylformamidines in the reaction of aminoazoles with N,N-dimethylformamide dimethyl acetal followed by the triazine ring closure with cyanamide affording therefore fused aminotriazines.
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