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[(QN)PYDZ] | 862305-18-8

中文名称
——
中文别名
——
英文名称
[(QN)PYDZ]
英文别名
4-[(R)-(6-chloropyridazin-3-yl)oxy-[(2S,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]methyl]-6-methoxyquinoline
[(QN)PYDZ]化学式
CAS
862305-18-8
化学式
C24H25ClN4O2
mdl
——
分子量
436.941
InChiKey
LTXNDFSZULGCGD-RNFQGHHASA-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):
    4.4
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    60.4
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    奎宁3,6-二氯哒嗪四丁基溴化铵potassium carbonate 作用下, 反应 0.17h, 以89%的产率得到[(QN)PYDZ]
    参考文献:
    名称:
    Facile Access to Mono-Cinchona Alkaloid-Derived Ligands
    摘要:
    Two facile accesses to mono-cinchona alkaloid-derived ligands, by conventional heating conditions and solvent-free microwave irradiation, are described. 1,4-Dichlorophthalazine (PHAL) or 3,6-dichloropyridazine (PYDZ) reacted with quinine (QN), cinchonine (CN), or cinchonidine (CND) by using CaH2 as acid-bonding reagent in DMF at 90-100C to provide mono-cinchona alkaloid-derived ligands 2a-f (87-95%) in 1.5h. However, the coupling reactions were performed under solvent-free microwave conditions to yield 2a-f (64-89%) within 15min.
    DOI:
    10.1080/00397910802323114
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文献信息

  • Facile Access to Mono-Cinchona Alkaloid-Derived Ligands
    作者:Hai-Bo Wang、Xiao-Li Sun、Ping-An Wang、Quan-Jun Wang、Peng-Juan Nan、Lin-Lin Jing
    DOI:10.1080/00397910802323114
    日期:2008.11.3
    Two facile accesses to mono-cinchona alkaloid-derived ligands, by conventional heating conditions and solvent-free microwave irradiation, are described. 1,4-Dichlorophthalazine (PHAL) or 3,6-dichloropyridazine (PYDZ) reacted with quinine (QN), cinchonine (CN), or cinchonidine (CND) by using CaH2 as acid-bonding reagent in DMF at 90-100C to provide mono-cinchona alkaloid-derived ligands 2a-f (87-95%) in 1.5h. However, the coupling reactions were performed under solvent-free microwave conditions to yield 2a-f (64-89%) within 15min.
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