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<4-chloro-6-<(2,3-dimethylphenyl)amino>-2-(4-methoxybenzyl)thio>pyrimidine | 86627-08-9

中文名称
——
中文别名
——
英文名称
<4-chloro-6-<(2,3-dimethylphenyl)amino>-2-(4-methoxybenzyl)thio>pyrimidine
英文别名
2-p-methoxybenzylthio-4-chloro-6-(2,3-xylidino)-pyrimidine;{4-chloro-6-[(2,3-dimethylphenyl)amino]-2-(4-methoxybenzyl)thio}pyrimidine;6-chloro-N-(2,3-dimethylphenyl)-2-[(4-methoxyphenyl)methylsulfanyl]pyrimidin-4-amine
<4-chloro-6-<(2,3-dimethylphenyl)amino>-2-(4-methoxybenzyl)thio>pyrimidine化学式
CAS
86627-08-9
化学式
C20H20ClN3OS
mdl
——
分子量
385.917
InChiKey
DQRMHOWHVCOJGO-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

  • 熔点:
    118-119 °C(Solv: benzene (71-43-2); hexane (110-54-3))
  • 沸点:
    546.2±50.0 °C(Predicted)
  • 密度:
    1.29±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    72.3
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:c23fb037d752f88c45c5c3bd1ece069b
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    <4-chloro-6-<(2,3-dimethylphenyl)amino>-2-(4-methoxybenzyl)thio>pyrimidine苯甲醚 作用下, 以 三氟乙酸 为溶剂, 反应 0.83h, 以89.1%的产率得到2-Mercapto-4-chloro-6-(2,3-xylidino)-pyrimidine
    参考文献:
    名称:
    Novel pyrimidine and 1,3,5-triazine hypolipemic agents
    摘要:
    New compounds were synthesized by changing the substituents of a trisubstituted pyrimidine, i.e., [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]thio] acetic acid, a potent hypolipidemic agent, impaired, however, by a marked hepatomegaly-inducing effect. The structural variations led to the subsidence (14b, i.e., 4-chloro-2-(dimethylamino)-6-[(2,3-dimethylphenyl)amino]pyrimidine) or to the reduction (18b, [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]amino] acetic acid) of said untoward effect but still maintained the hypolipidemic effect that, although markedly decreased, still proves significant for serum cholesterol and triglycerides (18b) or for serum triglycerides only (14b).
    DOI:
    10.1021/jm00378a016
  • 作为产物:
    参考文献:
    名称:
    Novel pyrimidine and 1,3,5-triazine hypolipemic agents
    摘要:
    New compounds were synthesized by changing the substituents of a trisubstituted pyrimidine, i.e., [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]thio] acetic acid, a potent hypolipidemic agent, impaired, however, by a marked hepatomegaly-inducing effect. The structural variations led to the subsidence (14b, i.e., 4-chloro-2-(dimethylamino)-6-[(2,3-dimethylphenyl)amino]pyrimidine) or to the reduction (18b, [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]amino] acetic acid) of said untoward effect but still maintained the hypolipidemic effect that, although markedly decreased, still proves significant for serum cholesterol and triglycerides (18b) or for serum triglycerides only (14b).
    DOI:
    10.1021/jm00378a016
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文献信息

  • Pyrimidine and s-triazine derivatives with antilipidemic activity
    申请人:LBP Istituto Faraceutico S.p.A.
    公开号:US04559345A1
    公开(公告)日:1985-12-17
    Pyrimidine and s-triazine derivatives of formula (I) ##STR1## in which X=CH or N; Y=for example halogen, alkoxy; W=for example --S--CH.sub.2 --COOH, --O--CH.sub.2 --COO alkyl, --NH--CH.sub.2 --CONHCH.sub.2 CH.sub.2 OH; Z=for example 2,3-xylidino, and methods for the preparation thereof are described. The compounds show high antilipemic activity.
    公式(I)的嘧啶和s-三嗪衍生物如下:##STR1## 其中X=CH或N;Y=例如卤素、烷氧基;W=例如--S--CH.sub.2 --COOH、--O--CH.sub.2 --COO烷基、--NH--CH.sub.2 --CONHCH.sub.2 CH.sub.2 OH;Z=例如2,3-二甲苯胺基,以及其制备方法。这些化合物表现出高抗脂质活性。
  • Novel pyrimidine and s. triazine derivatives with antilipidemic activity
    申请人:LPB Istituto Farmaceutico s.p.a.
    公开号:EP0073328A1
    公开(公告)日:1983-03-09
    Pyrimidine and s-triazine derivatives of formula (I) in which X = CH or N; Y = for example halogen, alkoxy; W = for example -S-CH2-COOH, -O-CH2-COO alkyl, -NH-CH2-CONHCH2CH2OH; Z = for example 2,3-xylidino, and methods for the preparation thereof are described. The compounds show high antiiipemic activity.
    式(I)的嘧啶和 s-三嗪衍生物 其中 X = CH 或 N;Y = 例如卤素、烷氧基;W = 例如 -S-CH2-COOH、-O-CH2-COO 烷基、-NH-CH2-CONHCH2CH2OH;Z = 例如 2,3-xylidino。这些化合物具有很高的抗血脂活性。
  • DATRI, G.;GOMARASCA, P.;RESNATI, G.;TRONCONI, G.;SCOLASTICO, C.;SIRTORI, +, J. MED. CHEM., 1984, 27, N 12, 1621-1629
    作者:DATRI, G.、GOMARASCA, P.、RESNATI, G.、TRONCONI, G.、SCOLASTICO, C.、SIRTORI, +
    DOI:——
    日期:——
  • US4559345A
    申请人:——
    公开号:US4559345A
    公开(公告)日:1985-12-17
  • Novel pyrimidine and 1,3,5-triazine hypolipemic agents
    作者:Gaetano D'Atri、Piero Gomarasca、Giuseppe Resnati、Giovanni Tronconi、Carlo Scolastico、Cesare R. Sirtori
    DOI:10.1021/jm00378a016
    日期:1984.12
    New compounds were synthesized by changing the substituents of a trisubstituted pyrimidine, i.e., [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]thio] acetic acid, a potent hypolipidemic agent, impaired, however, by a marked hepatomegaly-inducing effect. The structural variations led to the subsidence (14b, i.e., 4-chloro-2-(dimethylamino)-6-[(2,3-dimethylphenyl)amino]pyrimidine) or to the reduction (18b, [[4-chloro-6-[(2,3-dimethylphenyl)amino]-2-pyrimidinyl]amino] acetic acid) of said untoward effect but still maintained the hypolipidemic effect that, although markedly decreased, still proves significant for serum cholesterol and triglycerides (18b) or for serum triglycerides only (14b).
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