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Trifluoroacetyl substituted pyrazolotriazines: synthesis and pathways of formation
Mendeleev Communications Pub Date : 2020-03-01 , DOI: 10.1016/j.mencom.2020.03.016
Elena V. Sadchikova , Daria L. Alexeeva , Valentine G. Nenajdenko

The reaction of 4-dimethylamino-1,1,1-trifluorobut-3-en-2one with 3-arylpyrazole-5-diazonium salt in MeCN affords 7-aryl-3-(trifluoroacetyl)pyrazolo[5,1-c][1,2,4]triazines. The transformation of relative 5-diazopyrazoles leads to 4-hydroxy-1,4-dihydropyrazolo[5,1-c][1,2,4]triazine derivatives, while the reaction in acidic aqueous solution results in 4,4,4-trifluoro-3-oxo-2-(pyrazol-5-ylhydrazono)butanals.

中文翻译:

三氟乙酰基取代的吡唑并三嗪:合成及其形成途径

4-二甲氨基-1,1,1-三氟丁-3-烯-2酮与3-芳基吡唑-5-重氮盐在MeCN中的反应得到7-芳基-3-(三氟乙酰基)吡唑并[5,1-c] [ 1,2,4]三嗪。相对的5-重氮吡唑的转化产生4-羟基-1,4-二氢吡唑并[5,1-c] [1,2,4]三嗪衍生物,而在酸性水溶液中的反应产生4,4,4-三氟-3-氧代-2-(吡唑-5-基肼基)丁醛。
更新日期:2020-03-01
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