ethyl 3-cyano-1-methylindole-2-carboxylate | 155091-39-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: ethyl 3-cyano-1-methylindole-2-carboxylate
• 英文别名: Ethyl 3-cyano-1-methyl-indole-2-carboxylate
• CAS: 155091-39-7
• 化学式: C₁₃H₁₂N₂O₂
• 分子量: 228.25
• InChiKey: PLWBDMRJTBCBDW-UHFFFAOYSA-N

物化性质

• 沸点：
  427.8±30.0 °C(predicted)
• 密度：
  1.17±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  55
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  ethyl 3-cyano-1-methylindole-2-carboxylate 在 sodium hydroxide 作用下， 反应 7.0h， 以52%的产率得到1-methyl-1H-indole-2,3-dicarboxylic acid
  参考文献：
  名称：

  Potentially tautomeric 1,2,3,4-tetrahydro-1,4-dioxo-5H-pyridazino[4,5-bindole

  摘要：

  The tautomeric 1,4-dioxygenated pyridazinoindole 1 exists in aqueous solution as a mixture of all four tautomeric forms 1a - 1d, The predominant tautomeric form is the 4-hydroxy-1-oxo compound 1b. The relative abundance of the four forms 1a reversible arrow 1b reversible arrow 1c reversible arrow 1d at equilibrium is 10(4.93):10(8.03):10(3.61):1.

  DOI：

  10.1016/s0040-4020(01)81802-0
• 作为产物：
  描述：

  乙基3-甲酰基-1-甲基-1H-吲哚-2-羧酸酯 在 盐酸羟胺 作用下， 以 甲酸 为溶剂， 反应 0.5h， 以94%的产率得到ethyl 3-cyano-1-methylindole-2-carboxylate
  参考文献：
  名称：

  Potentially tautomeric 1,2,3,4-tetrahydro-1,4-dioxo-5H-pyridazino[4,5-bindole

  摘要：

  The tautomeric 1,4-dioxygenated pyridazinoindole 1 exists in aqueous solution as a mixture of all four tautomeric forms 1a - 1d, The predominant tautomeric form is the 4-hydroxy-1-oxo compound 1b. The relative abundance of the four forms 1a reversible arrow 1b reversible arrow 1c reversible arrow 1d at equilibrium is 10(4.93):10(8.03):10(3.61):1.

  DOI：

  10.1016/s0040-4020(01)81802-0

文献信息

• Indoles and pyridazino[4,5-b]indoles as nonnucleoside analog inhibitors of HIV-1 reverse transcriptase
  作者：M Font、A Monge、A Cuartero、A Elorriaga、J.J. Martínez-Irujo、E Alberdi、E Santiago、I Prieto、J.J. Lasarte、P Sarobe、F Borrás

  DOI：10.1016/0223-5234(96)88316-4

  日期：1995.1

  The synthesis and the study of the activity of new indol-2-carboxamides and pyridazino[4,5-b]indoles as inhibitors of HIV-1 reverse transcriptase (RT) are presented. The activity of the compounds synthesized as inhibitors of different types of HIV-1 RT (wild type enzyme and mutant forms P236L, Y181C and P236L/Y181C) was evaluated. The activity of the most active compounds was investigated in the syncytia reduction in vitro assay, in HIV-1(IIIB)-infected HT4lacZ-1 cells. Their potential cytotoxicity was determined in parallel. Two lead compounds, N-[1-[2-(3-isopropylamino)pyridyl]piperazin]-5,6-methylenedioxy indol-2-carboxamide 7q and N-[1-[2-(3-ethylamino)pyridyl]piperazin] 7s have been identified.
• Potentially tautomeric 1,2,3,4-tetrahydro-1,4-dioxo-5H-pyridazino[4,5-bindole
  作者：Alâattin Güven、R.Alan Jones

  DOI：10.1016/s0040-4020(01)81802-0

  日期：1993.1

  The tautomeric 1,4-dioxygenated pyridazinoindole 1 exists in aqueous solution as a mixture of all four tautomeric forms 1a - 1d, The predominant tautomeric form is the 4-hydroxy-1-oxo compound 1b. The relative abundance of the four forms 1a reversible arrow 1b reversible arrow 1c reversible arrow 1d at equilibrium is 10(4.93):10(8.03):10(3.61):1.