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5-(4-Amino-phenyl)-6-octyl-pyrimidine-2,4-diamine | 885040-94-8

中文名称
——
中文别名
——
英文名称
5-(4-Amino-phenyl)-6-octyl-pyrimidine-2,4-diamine
英文别名
5-(4-aminophenyl)-6-octylpyrimidine-2,4-diamine
5-(4-Amino-phenyl)-6-octyl-pyrimidine-2,4-diamine化学式
CAS
885040-94-8
化学式
C18H27N5
mdl
——
分子量
313.446
InChiKey
PIYSKTRNJSZHRR-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):
    3.79
  • 重原子数:
    23.0
  • 可旋转键数:
    8.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    103.84
  • 氢给体数:
    3.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    5-(4-Amino-phenyl)-6-octyl-pyrimidine-2,4-diamine对甲砜基苯甲醛sodium acetate 、 sodium cyanoborohydride 、 溶剂黄146 作用下, 以 甲醇 为溶剂, 以70%的产率得到5-[4-(4-Methanesulfonyl-benzylamino)-phenyl]-6-octyl-pyrimidine-2,4-diamine
    参考文献:
    名称:
    Optimization of 2,4-diaminopyrimidines as GHS-R antagonists: Side chain exploration
    摘要:
    The synthesis and structure-activity relationships of the 4- and 6-substituents of 2,4-diaminopyrimidine-based growth hormone secretagogue receptor (GHS-R) antagonists are described. Diaminopyrimidines with 6-norbornenyl (4n) and 6-tetrahydrofuranyl (4p) substitutents were found to exhibit potent GHS-R antagonism and good selectivity (similar to 1000-fold) against dihydrofolate reductase. (C) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.01.012
  • 作为产物:
    描述:
    5-(4-Nitro-phenyl)-6-octyl-pyrimidine-2,4-diaminepalladium dihydroxide 氢气 作用下, 以 甲醇 为溶剂, 以95%的产率得到5-(4-Amino-phenyl)-6-octyl-pyrimidine-2,4-diamine
    参考文献:
    名称:
    Optimization of 2,4-diaminopyrimidines as GHS-R antagonists: Side chain exploration
    摘要:
    The synthesis and structure-activity relationships of the 4- and 6-substituents of 2,4-diaminopyrimidine-based growth hormone secretagogue receptor (GHS-R) antagonists are described. Diaminopyrimidines with 6-norbornenyl (4n) and 6-tetrahydrofuranyl (4p) substitutents were found to exhibit potent GHS-R antagonism and good selectivity (similar to 1000-fold) against dihydrofolate reductase. (C) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.01.012
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