ethyl 2-[(5-acetyl-4-methyl-2-(2-oxopropylsulfanyl)thiophene-3-carbonyl)amino]-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate | 872133-07-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩类
• 英文名称: ethyl 2-[(5-acetyl-4-methyl-2-(2-oxopropylsulfanyl)thiophene-3-carbonyl)amino]-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
• 英文别名: Ethyl 2-[[5-acetyl-4-methyl-2-(2-oxopropylsulfanyl)thiophene-3-carbonyl]amino]-5,5-dimethyl-7-oxo-4,6-dihydro-1-benzothiophene-3-carboxylate
• CAS: 872133-07-8
• 化学式: C₂₄H₂₇NO₆S₃
• 分子量: 521.679
• InChiKey: VWBQBEBHSVNQEM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  34
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  188
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  ethyl 2-[(5-acetyl-4-methyl-2-(2-oxopropylsulfanyl)thiophene-3-carbonyl)amino]-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 在 一水合肼 、 三乙胺 作用下， 以 1,4-二氧六环 、 N,N-二甲基甲酰胺 为溶剂， 反应 9.0h， 生成 ethyl 2-[5-(1-hydrazonoethyl)-4-methyl-3-oxo-1,3-dihydrothieno[2,3-c]pyrazol-2-yl]-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
  参考文献：
  名称：

  Studies on 2-Aminothiophenes: Synthesis, Transformations, and Biological Evaluation of Functionally-Substituted Thiophenes and Their Fused Derivatives

  摘要：

  Heterocyclic enamines 1 reacted with ethyl acetoacetate to afford the corresponding amide derivatives 2. Treatment of 2 with carbon disulphide yielded the dipotassium salts 3 which reacted in-situ with a variety of alpha-haloketones to give the respective substititted thiophenes 5, 8, and 13. Die reactivity of the latter products towards various chemical reagents was studied to yield their fused thiophene derivatives 7, 10, 12, and 14, respectively. Some representative compounds were tested for antimicrobial activity.

  DOI：

  10.1080/104265090517406
• 作为产物：
  描述：

  ethyl 2-(acetoacetamido)-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 在 氢氧化钾 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 生成 ethyl 2-[(5-acetyl-4-methyl-2-(2-oxopropylsulfanyl)thiophene-3-carbonyl)amino]-5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
  参考文献：
  名称：

  Studies on 2-Aminothiophenes: Synthesis, Transformations, and Biological Evaluation of Functionally-Substituted Thiophenes and Their Fused Derivatives

  摘要：

  Heterocyclic enamines 1 reacted with ethyl acetoacetate to afford the corresponding amide derivatives 2. Treatment of 2 with carbon disulphide yielded the dipotassium salts 3 which reacted in-situ with a variety of alpha-haloketones to give the respective substititted thiophenes 5, 8, and 13. Die reactivity of the latter products towards various chemical reagents was studied to yield their fused thiophene derivatives 7, 10, 12, and 14, respectively. Some representative compounds were tested for antimicrobial activity.

  DOI：

  10.1080/104265090517406

文献信息

• Studies on 2-Aminothiophenes: Synthesis, Transformations, and Biological Evaluation of Functionally-Substituted Thiophenes and Their Fused Derivatives
  作者：Wagnat W. Wardakhan、Hatem M. Gaber、Salama A. Ouf、Sherif M. Sherif

  DOI：10.1080/104265090517406

  日期：2005.2

  Heterocyclic enamines 1 reacted with ethyl acetoacetate to afford the corresponding amide derivatives 2. Treatment of 2 with carbon disulphide yielded the dipotassium salts 3 which reacted in-situ with a variety of alpha-haloketones to give the respective substititted thiophenes 5, 8, and 13. Die reactivity of the latter products towards various chemical reagents was studied to yield their fused thiophene derivatives 7, 10, 12, and 14, respectively. Some representative compounds were tested for antimicrobial activity.