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diethyl 5,8-diamino-2-methylsulfanyl-6a,7-dihydro-6H-1,3,6,7-tetraazaphenalene-4,9-dicarboxylate picrate | 1447839-77-1

中文名称
——
中文别名
——
英文名称
diethyl 5,8-diamino-2-methylsulfanyl-6a,7-dihydro-6H-1,3,6,7-tetraazaphenalene-4,9-dicarboxylate picrate
英文别名
——
diethyl 5,8-diamino-2-methylsulfanyl-6a,7-dihydro-6H-1,3,6,7-tetraazaphenalene-4,9-dicarboxylate picrate化学式
CAS
1447839-77-1
化学式
C6H3N3O7*C16H20N6O4S
mdl
——
分子量
621.544
InChiKey
AJDJRNAFKYGFRU-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):
    0.9
  • 重原子数:
    43.0
  • 可旋转键数:
    8.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    304.13
  • 氢给体数:
    5.0
  • 氢受体数:
    18.0

反应信息

  • 作为反应物:
    描述:
    diethyl 5,8-diamino-2-methylsulfanyl-6a,7-dihydro-6H-1,3,6,7-tetraazaphenalene-4,9-dicarboxylate picrate氧气sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 1.0h, 以90%的产率得到diethyl 5,8-diamino-2-methylsulfanyl-6H-1,3,6,7-tetraazaphenalene-4,9-dicarboxylate
    参考文献:
    名称:
    Reaction of ethyl 3,3-diaminoacrylate with pyrimidine series o-chloro ketones. Synthesis of pyrido[4,3-d]pyrimidines and 6H-1,3,6,7-tetra-azaphenalenes
    摘要:
    Cyclocondensation of ethyl 3,3-diaminoacrylate with 5-acetyl-4-chloropyrimidines gave ortho- and peri-condensed heterocycles formed through substitution of the chlorine atom by the alpha-carbon atom of the enediamine and condensation of the amino group with the carbonyl or by addition of the amino group to the pyridine ring.
    DOI:
    10.1007/s10593-013-1269-2
  • 作为产物:
    参考文献:
    名称:
    Reaction of ethyl 3,3-diaminoacrylate with pyrimidine series o-chloro ketones. Synthesis of pyrido[4,3-d]pyrimidines and 6H-1,3,6,7-tetra-azaphenalenes
    摘要:
    Cyclocondensation of ethyl 3,3-diaminoacrylate with 5-acetyl-4-chloropyrimidines gave ortho- and peri-condensed heterocycles formed through substitution of the chlorine atom by the alpha-carbon atom of the enediamine and condensation of the amino group with the carbonyl or by addition of the amino group to the pyridine ring.
    DOI:
    10.1007/s10593-013-1269-2
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