摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(3,4,5-trimethoxyphenyl)-4,6-diphenylpyrimidine | 1529532-05-5

中文名称
——
中文别名
——
英文名称
2-(3,4,5-trimethoxyphenyl)-4,6-diphenylpyrimidine
英文别名
4,6-diphenyl-2-(3,4,5-trimethoxyphenyl)pyrimidine;4,6-Diphenyl-2-(3,4,5-trimethoxyphenyl)pyrimidine
2-(3,4,5-trimethoxyphenyl)-4,6-diphenylpyrimidine化学式
CAS
1529532-05-5
化学式
C25H22N2O3
mdl
——
分子量
398.461
InChiKey
OARQYTCGMHQTHZ-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):
    5.1
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    53.5
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    3,4,5-三甲氧基苯甲醛吡啶potassium carbonate 、 sodium hydroxide 作用下, 以 二氯甲烷二甲基亚砜叔丁醇 为溶剂, 反应 4.0h, 生成 2-(3,4,5-trimethoxyphenyl)-4,6-diphenylpyrimidine
    参考文献:
    名称:
    Efficient and Benign One-Pot Conversion of N-Tosyl-1,4,5,6-tetrahydropyrimidines to Pyrimidines via Tandem β-Elimination and Aromatization
    摘要:
    An efficient, mild, benign, and practical method for one-pot conversion of N-tosyl-1,4,5,6-tetrahydropyrimidines into pyrimidines is discussed in detail. In this method, N-tosyl-1,4,5,6-tetrahydropyrimidines are first prepared via N-tosylation of tetrahydropyrimidines with TsCl and then treated with 1.5 equivalents of NaOH in dimethylsulfoxide (DMSO) under air at 60 degrees C to afford corresponding pyrimidines in 70-95% yields via cascade -elimination and aromatization. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resources: Full experimental and spectral details.]
    DOI:
    10.1080/00397911.2013.764433
点击查看最新优质反应信息

文献信息

  • Novel multi-component syntheses of pyrimidines using β-CD in aqueous medium
    作者:Chowrasia Rakhi、Katla Ramesh、Mariana P. Darbem、Tabata A. Branquinho、Aline Rufino de Oliveira、Padma Sunitha Manjari、Nelson Luís C. Domingues
    DOI:10.1016/j.tetlet.2016.02.106
    日期:2016.4
    Using β-cyclodextrin (β-CD) as a catalyst pyrimidine derivatives were synthesized for the first time in aqueous medium. β-CD is a recyclable, inexpensive, economically viable, non-toxic, and readily available material. Various aldehydes were used with ammonium acetate, and 1,3-diketones to generate a series of pyrimidine derivatives in good to excellent yields.
    以β-环糊精(β-CD)为催化剂,在介质中首次合成了嘧啶生物。β-CD是一种可回收,廉价,经济可行,无毒且易于获得的材料。各种醛与乙酸铵和1,3-二酮一起使用可生成一系列嘧啶生物,收率好至极好。
查看更多