2-Ethoxy-4-methylsulfanyl-6-phenylpyrimidine-5-carbonitrile | 211687-26-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-Ethoxy-4-methylsulfanyl-6-phenylpyrimidine-5-carbonitrile
• CAS: 211687-26-2
• 化学式: C₁₄H₁₃N₃OS
• 分子量: 271.343
• InChiKey: DVINXGQBHGTKER-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  19
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  84.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-Ethoxy-4-methylsulfanyl-6-phenylpyrimidine-5-carbonitrile 在 一水合肼 作用下， 反应 3.0h， 以75%的产率得到6-hydrazino-4-phenyl-1(2)H-pyrazolo[3,4-d]pyrimidin-3-ylamine
  参考文献：
  名称：

  Synthesis of Thieno[2,3-d]pyrimidines and Aminopyrimidines from 2-Alkoxy-5-cyano-4-thioxopyrimidine Intermediates

  摘要：

  beta-Chloro-alpha-cyanocinnamonitrile reacts in an one-pot reaction with potassium thiocyanate and alkanol to form 2-allcoxy-6-phenyl-5-cyano-1,4-dihydro-4-pyrimidinthions. The products were S-alkylated to yield thieno[2,3-d]pyrimidines on cyclization and aminopyrimidines an substitution of alkoxy and alkylthio groups.

  DOI：

  10.3987/com-98-8117
• 作为产物：
  描述：

  alpha-氯苄亚基丙二腈 在 sodium hydroxide 作用下， 反应 4.0h， 生成 2-Ethoxy-4-methylsulfanyl-6-phenylpyrimidine-5-carbonitrile
  参考文献：
  名称：

  Synthesis of Thieno[2,3-d]pyrimidines and Aminopyrimidines from 2-Alkoxy-5-cyano-4-thioxopyrimidine Intermediates

  摘要：

  beta-Chloro-alpha-cyanocinnamonitrile reacts in an one-pot reaction with potassium thiocyanate and alkanol to form 2-allcoxy-6-phenyl-5-cyano-1,4-dihydro-4-pyrimidinthions. The products were S-alkylated to yield thieno[2,3-d]pyrimidines on cyclization and aminopyrimidines an substitution of alkoxy and alkylthio groups.

  DOI：

  10.3987/com-98-8117

文献信息

• Synthesis of Thieno[2,3-d]pyrimidines and Aminopyrimidines from 2-Alkoxy-5-cyano-4-thioxopyrimidine Intermediates
  作者：Matthias Rehwald、Karl Gewald

  DOI：10.3987/com-98-8117

  日期：——

  beta-Chloro-alpha-cyanocinnamonitrile reacts in an one-pot reaction with potassium thiocyanate and alkanol to form 2-allcoxy-6-phenyl-5-cyano-1,4-dihydro-4-pyrimidinthions. The products were S-alkylated to yield thieno[2,3-d]pyrimidines on cyclization and aminopyrimidines an substitution of alkoxy and alkylthio groups.

表征谱图