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-((2-(3-methoxyphenyl)-2-oxoethyl)thio)-N-phenylacetamide | 1216821-17-8

中文名称
——
中文别名
——
英文名称
2-((2-(3-methoxyphenyl)-2-oxoethyl)thio)-N-phenylacetamide
英文别名
2-[2-(3-methoxyphenyl)-2-oxoethyl]sulfanyl-N-phenylacetamide
2-((2-(3-methoxyphenyl)-2-oxoethyl)thio)-N-phenylacetamide化学式
CAS
1216821-17-8
化学式
C17H17NO3S
mdl
——
分子量
315.393
InChiKey
HXCQUTCOMDGLQS-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):
    3.2
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    80.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    聚合甲醛2-((2-(3-methoxyphenyl)-2-oxoethyl)thio)-N-phenylacetamide三乙胺 作用下, 以 1,4-二氧六环 为溶剂, 反应 20.0h, 以20%的产率得到2-((3-hydroxy-1-(3-methoxyphenyl)-1-oxopropan-2-yl)thio)-N-phenylacetamide
    参考文献:
    名称:
    A chemoselective hydroxymethylation: new route for the synthesis of 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones
    摘要:
    Treatment of 2-(2-oxo-2-arylethylthio)-N-(4H-1,2,4-triazol-3-yl)acetamides with paraformaldehyde in the presence of a base has led to a tandem chemoselective hydroxymethylation followed by cyclization yielding a set of novel 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones. The thiomorpholine ring has been found to have a boat like conformation in these compounds as evidenced by NOESY NMR spectrum. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.12.100
  • 作为产物:
    描述:
    苯胺potassium carbonate 作用下, 以 乙醇 为溶剂, 反应 9.0h, 生成 2-((2-(3-methoxyphenyl)-2-oxoethyl)thio)-N-phenylacetamide
    参考文献:
    名称:
    具有生物重要性的N-杂芳基-2-(杂芳硫基)乙酰胺的合成
    摘要:
    已经描述了具有通过连接中具有硫和氮的链连接的三唑和selena /噻二唑环的化合物的合成。所得的N-杂芳基-2-(杂芳硫基)乙酰胺可能具有重要的生物学意义,因为相关化合物可用于抑制HIV 1复制。
    DOI:
    10.1002/jhet.1804
点击查看最新优质反应信息

文献信息

  • A chemoselective hydroxymethylation: new route for the synthesis of 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones
    作者:Thulasiraman Krishnaraj、Shanmugam Muthusubramanian
    DOI:10.1016/j.tetlet.2011.12.100
    日期:2012.2
    Treatment of 2-(2-oxo-2-arylethylthio)-N-(4H-1,2,4-triazol-3-yl)acetamides with paraformaldehyde in the presence of a base has led to a tandem chemoselective hydroxymethylation followed by cyclization yielding a set of novel 6-aroyl-4-(4H-triazol-3-yl)thiomorpholin-3-ones. The thiomorpholine ring has been found to have a boat like conformation in these compounds as evidenced by NOESY NMR spectrum. (C) 2011 Elsevier Ltd. All rights reserved.
  • Synthesis of Biologically Important<i>N</i>-Heteroaryl-2-(heteroarylthio)acetamides
    作者:Thulasiraman Krishnaraj、Shanmugam Muthusubramanian
    DOI:10.1002/jhet.1804
    日期:2014.7
    The synthesis of compounds having triazole and selena/thiadiazole rings connected by a chain having sulfur and nitrogen in the link has been described. The resultant N‐heteroaryl‐2‐(heteroarylthio)acetamide may be biologically important as related compounds found application in the inhibition of HIV 1 replications.
    已经描述了具有通过连接中具有硫和氮的链连接的三唑和selena /噻二唑环的化合物的合成。所得的N-杂芳基-2-(杂芳硫基)乙酰胺可能具有重要的生物学意义,因为相关化合物可用于抑制HIV 1复制。
查看更多