ethyl 5-[N'-(1-ethoxycarbonyl-2-oxo-2-phenyl-ethylidene)-hydrazino]-3-phenyl-1H-pyrazole-4-carboxylate | 1649479-39-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: ethyl 5-[N'-(1-ethoxycarbonyl-2-oxo-2-phenyl-ethylidene)-hydrazino]-3-phenyl-1H-pyrazole-4-carboxylate
• CAS: 1649479-39-9
• 化学式: C₂₃H₂₂N₄O₅
• 分子量: 434.451
• InChiKey: XIBISTULPUUDPP-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  ethyl 5-[N'-(1-ethoxycarbonyl-2-oxo-2-phenyl-ethylidene)-hydrazino]-3-phenyl-1H-pyrazole-4-carboxylate 在 硫酸 作用下， 反应 24.0h， 以65%的产率得到4,7-diphenyl-pyrazolo[5,1-c]-1,2,4-triazine-3,8-dicarboxylic acid diethyl ester
  参考文献：
  名称：

  Further Studies with Ethyl 5-Amino-3-phenyl-lH-pyrazole-4-carboxylate¹

  摘要：

  The newly synthesized ethyl 3‐amino‐5‐phenylpyrazole‐4‐carboxylate 1 was diazotized and coupled with β‐naphthol, active methylene reagents 6, 9, 12, 15, and the active methine 19 to afford the pyrazolo[5,1‐c]triazines 5, 8, 11, 14, 17, 18, and the pyrazolo[5,1‐c]‐1,2,4‐triazoles 21, 22, and 23, respectively. Structures are elucidated and mechanisms are discussed.

  DOI：

  10.1002/jhet.1802
• 作为产物：
  描述：

  苯甲酰乙酸乙酯 、 5-氨基-3-苯基-1H-吡唑-4-羧酸乙酯 在 盐酸 、 sodium nitrite 、 sodium acetate 作用下， 以 水 、 溶剂黄146 、 乙醇 为溶剂， 以70%的产率得到ethyl 5-[N'-(1-ethoxycarbonyl-2-oxo-2-phenyl-ethylidene)-hydrazino]-3-phenyl-1H-pyrazole-4-carboxylate
  参考文献：
  名称：

  Further Studies with Ethyl 5-Amino-3-phenyl-lH-pyrazole-4-carboxylate¹

  摘要：

  The newly synthesized ethyl 3‐amino‐5‐phenylpyrazole‐4‐carboxylate 1 was diazotized and coupled with β‐naphthol, active methylene reagents 6, 9, 12, 15, and the active methine 19 to afford the pyrazolo[5,1‐c]triazines 5, 8, 11, 14, 17, 18, and the pyrazolo[5,1‐c]‐1,2,4‐triazoles 21, 22, and 23, respectively. Structures are elucidated and mechanisms are discussed.

  DOI：

  10.1002/jhet.1802