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2-amino-4-methyl-1,2-dihydropyrimido[5.4-c]quinolin-5(6H)-one | 1260092-72-5

中文名称
——
中文别名
——
英文名称
2-amino-4-methyl-1,2-dihydropyrimido[5.4-c]quinolin-5(6H)-one
英文别名
2-amino-4-methyl-6H-pyrimido[5,4-c]quinolin-5-one
2-amino-4-methyl-1,2-dihydropyrimido[5.4-c]quinolin-5(6H)-one化学式
CAS
1260092-72-5
化学式
C12H10N4O
mdl
——
分子量
226.238
InChiKey
BLFDBOUKKHISHY-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):
    0.8
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    80.9
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-乙酰基-4-羟基喹啉-2(1h)-酮硝酸胍sodium acetate 作用下, 以 乙醇 为溶剂, 反应 8.0h, 以85%的产率得到2-amino-4-methyl-1,2-dihydropyrimido[5.4-c]quinolin-5(6H)-one
    参考文献:
    名称:
    Synthesis, antioxidant and toxicological study of novel pyrimido quinoline derivatives from 4-hydroxy-3-acyl quinolin-2-one
    摘要:
    A series of novel pyrimido and other fused quinoline derivatives like 4-methyl pyrimido [5,4-c]quinoline-2,5(1H,6H)-dione (4a), 4-methyl-2-thioxo-1,2-dihydropyrimido [5,4-c]quinoline-5(6H)-one (4b), 2-amino-4-methyl-1,2-dihydropyrimido [5,4-c]quinolin-5(6H)-one (4c), 3-methylisoxazolo [4,5-c]quinolin-4(5H)-one (4d), 3-methyl-1H-pyrazolo [4,3-c]quinoline-4(5H)-one (5e), 5-methyl-1H-[1,2,4] triazepino [6,5-c]quinoline-2,6(3H,7H)-dione (5f), 5-methyl-2-thioxo-2,3-dihydro-1H-[1,2,4]triazepino [6,5-c]quinolin-6(7H)one (5g) were synthesized regioselectively from 4-hydroxy-3-acyl quinolin-2-one 3. They were screened for their in vitro antioxidant activities against radical scavenging capacity using DPPH, Trolox equivalent antioxidant capacity (TEAC), total antioxidant activity by FRAP, superoxide radical (O-2(degrees-)) scavenging activity, metal chelating activity and nitric oxide scavenging activity. Among the compounds screened, 4c and 5g exhibited significant antioxidant activities. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.09.018
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