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1-(3,4-Dichlorophenyl)-2-[4-[3-(diethylaminomethyl)-4-hydroxyanilino]-6-phenylpyrimidin-2-yl]guanidine | 86196-43-2

中文名称
——
中文别名
——
英文名称
1-(3,4-Dichlorophenyl)-2-[4-[3-(diethylaminomethyl)-4-hydroxyanilino]-6-phenylpyrimidin-2-yl]guanidine
英文别名
1-(3,4-dichlorophenyl)-2-[4-[3-(diethylaminomethyl)-4-hydroxyanilino]-6-phenylpyrimidin-2-yl]guanidine
1-(3,4-Dichlorophenyl)-2-[4-[3-(diethylaminomethyl)-4-hydroxyanilino]-6-phenylpyrimidin-2-yl]guanidine化学式
CAS
86196-43-2
化学式
C28H29Cl2N7O
mdl
——
分子量
550.491
InChiKey
NGZSWFCTOYYVAH-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):
    6
  • 重原子数:
    38
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    112
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    Sodium; 2-cyanoamino-6-phenyl-pyrimidin-4-olate 在 盐酸乙二醇乙醚sodium hydroxide三氯氧磷 作用下, 以 为溶剂, 生成 1-(3,4-Dichlorophenyl)-2-[4-[3-(diethylaminomethyl)-4-hydroxyanilino]-6-phenylpyrimidin-2-yl]guanidine
    参考文献:
    名称:
    Synthesis and antifilarial activity of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]-2-pyrimidinyl]-N'-phenylguanidines
    摘要:
    A series of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]- 2-pyrimidinyl]-N'-phenylguanidines have been synthesized for antifilarial evaluation. Reaction of the appropriate benzenamines with N-cyanoguanidine, followed by condensation of the resultant N-phenylimidodicarbonimidic diamides (V) with ethyl 4,4,4-trifluoro-3-oxobutanoate provided the intermediate N-(4-hydroxy-2-pyrimidinyl)-N'-phenylguanidines VIa. Alternatively, compounds VIa were synthesized by reaction of the requisite beta-keto esters (VII) with N-cyanoguanidine to give the (4-hydroxy-2-pyrimidinyl)cyanamides (VIII), followed by treatment with the desired benzenamines. Chlorination with POCl3 and condensation with the appropriate benzenamines (IX) generated the desired guanidines (X). Antifilarial activity was confined to adult Litomosoides carinii infections, and a structure-activity relationship for this activity is discussed. Lack of activity against L. carinii microfilaria and adult Brugia pahangi infections preclude further work in this area pending evaluation in additional experimental models.
    DOI:
    10.1021/jm00363a010
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文献信息

  • Synthesis and antifilarial activity of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]-2-pyrimidinyl]-N'-phenylguanidines
    作者:Mario Angelo、Daniel Ortwine、Donald Worth、Leslie M. Werbel、John W. McCall
    DOI:10.1021/jm00363a010
    日期:1983.9
    A series of N-[4-[[4-alkoxy-3-[(dialkylamino)methyl]phenyl]amino]- 2-pyrimidinyl]-N'-phenylguanidines have been synthesized for antifilarial evaluation. Reaction of the appropriate benzenamines with N-cyanoguanidine, followed by condensation of the resultant N-phenylimidodicarbonimidic diamides (V) with ethyl 4,4,4-trifluoro-3-oxobutanoate provided the intermediate N-(4-hydroxy-2-pyrimidinyl)-N'-phenylguanidines VIa. Alternatively, compounds VIa were synthesized by reaction of the requisite beta-keto esters (VII) with N-cyanoguanidine to give the (4-hydroxy-2-pyrimidinyl)cyanamides (VIII), followed by treatment with the desired benzenamines. Chlorination with POCl3 and condensation with the appropriate benzenamines (IX) generated the desired guanidines (X). Antifilarial activity was confined to adult Litomosoides carinii infections, and a structure-activity relationship for this activity is discussed. Lack of activity against L. carinii microfilaria and adult Brugia pahangi infections preclude further work in this area pending evaluation in additional experimental models.
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