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4-Amino-6-methoxy-2-methylpyrimidine-5-carbaldehyde | 76574-48-6

中文名称
——
中文别名
——
英文名称
4-Amino-6-methoxy-2-methylpyrimidine-5-carbaldehyde
英文别名
4-amino-6-methoxy-2-methylpyrimidine-5-carbaldehyde
4-Amino-6-methoxy-2-methylpyrimidine-5-carbaldehyde化学式
CAS
76574-48-6
化学式
C7H9N3O2
mdl
——
分子量
167.167
InChiKey
XTMPMSGWGNAOFG-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:
    350.0±42.0 °C(Predicted)
  • 密度:
    1.284±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    78.1
  • 氢给体数:
    1
  • 氢受体数:
    5

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

反应信息

  • 作为产物:
    描述:
    4-hydroxy-2-methyl-6-oxo-1H-pyrimidine-5-carboxamide 甲酸乙醇氢气N,N-二甲基苯胺三氯氧磷 作用下, 以 甲醇 为溶剂, 25.0 ℃ 、344.73 kPa 条件下, 反应 5.0h, 生成 4-Amino-6-methoxy-2-methylpyrimidine-5-carbaldehyde
    参考文献:
    名称:
    Antihypertensive activity of 6-arylpyrido[2,3-d]pyrimidin-7-amine derivatives
    摘要:
    A series of 51 6-arylpyrido[2,3-d]pyrimidin-7-amine derivatives was prepared and evaluated for antihypertensive activity in the conscious spontaneously hypertensive rat. A number of these compounds, notably 6-(2,6-dichlorophenyl)-2-methylpyrido[2,3-d]pyrimidin-7-amine (36), lowered blood pressure in these rats in a gradual and sustained manner to normotensive levels at oral doses of 10-50 mg/kg. Normalized blood pressure levels could then be maintained by single daily oral doses. The effect of structural variation in the 6-aryl group and in the 2 and 4 positions of the pyridopyrimidine ring on activity is reported and discussed.
    DOI:
    10.1021/jm00136a006
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文献信息

  • Antihypertensive activity of 6-arylpyrido[2,3-d]pyrimidin-7-amine derivatives
    作者:Lawrence R. Bennett、C. John Blankley、Robert W. Fleming、Ronald D. Smith、Deirdre K. Tessman
    DOI:10.1021/jm00136a006
    日期:1981.4
    A series of 51 6-arylpyrido[2,3-d]pyrimidin-7-amine derivatives was prepared and evaluated for antihypertensive activity in the conscious spontaneously hypertensive rat. A number of these compounds, notably 6-(2,6-dichlorophenyl)-2-methylpyrido[2,3-d]pyrimidin-7-amine (36), lowered blood pressure in these rats in a gradual and sustained manner to normotensive levels at oral doses of 10-50 mg/kg. Normalized blood pressure levels could then be maintained by single daily oral doses. The effect of structural variation in the 6-aryl group and in the 2 and 4 positions of the pyridopyrimidine ring on activity is reported and discussed.
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