methyl 2-((3-(4-methoxyphenyl)-4-oxo-2-((2-(trimethylsilyl)ethoxy)methyl)-2,4-dihydroindeno[1,2-c]pyrazol-5-yl)carbamoyl)hydrazine-1-carboxylate | 807628-39-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: methyl 2-((3-(4-methoxyphenyl)-4-oxo-2-((2-(trimethylsilyl)ethoxy)methyl)-2,4-dihydroindeno[1,2-c]pyrazol-5-yl)carbamoyl)hydrazine-1-carboxylate
• CAS: 807628-39-3
• 化学式: C₂₆H₃₁N₅O₆Si
• 分子量: 537.648
• InChiKey: AJRPRGTVMREZHY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.47
• 重原子数：
  38.0
• 可旋转键数：
  8.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  132.81
• 氢给体数：
  3.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  methyl 2-((3-(4-methoxyphenyl)-4-oxo-2-((2-(trimethylsilyl)ethoxy)methyl)-2,4-dihydroindeno[1,2-c]pyrazol-5-yl)carbamoyl)hydrazine-1-carboxylate 在 盐酸 作用下， 以 1,4-二氧六环 、 乙醇 为溶剂， 反应 0.5h， 生成 3-(4-methoxyphenyl)-5-(2-methoxycarbonylhydrazinecarboxamido)indeno[1,2-c]pyrazol-4-one
  参考文献：
  名称：

  Parallel synthesis of acylsemicarbazide libraries: preparation of potent cyclin dependent kinase (cdk) inhibitors

  摘要：

  Potent cyclin dependent kinase inhibitors were prepared using parallel synthesis methodology. Treating advanced intermediate 2 with a variety of hydrazides in DMSO at 80degreesC for 30 min gave the desired acylsemicarbazides in good to excellent yield. Several compounds were active against cdk4/D1 and cdk2/E in the low nanomolar range. The SAR indicates a wide variety of substituents are tolerated at the acylsemicarbazide moiety. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.09.023
• 作为产物：
  描述：

  5-氨基-3-(4-甲氧基苯基)-茚并[1,2-c]吡唑-4(2H)-酮 在 potassium carbonate 、 三乙胺 作用下， 以 氯仿 、 二甲基亚砜 、 丙酮 为溶剂， 生成 methyl 2-((3-(4-methoxyphenyl)-4-oxo-2-((2-(trimethylsilyl)ethoxy)methyl)-2,4-dihydroindeno[1,2-c]pyrazol-5-yl)carbamoyl)hydrazine-1-carboxylate
  参考文献：
  名称：

  Parallel synthesis of acylsemicarbazide libraries: preparation of potent cyclin dependent kinase (cdk) inhibitors

  摘要：

  Potent cyclin dependent kinase inhibitors were prepared using parallel synthesis methodology. Treating advanced intermediate 2 with a variety of hydrazides in DMSO at 80degreesC for 30 min gave the desired acylsemicarbazides in good to excellent yield. Several compounds were active against cdk4/D1 and cdk2/E in the low nanomolar range. The SAR indicates a wide variety of substituents are tolerated at the acylsemicarbazide moiety. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.09.023