戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 402478作成日:2026年10月26日

Ethyl 4,4,4-trifluoroacetoacetate → 1-methyl-3-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-6(7H)-one

https://huagongshe.com/reaction/402478

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4,4,4-trifluoroacetoacetateHCID 67793—
反応物1-Methyl-3-phenyl-1H-pyrazol-5-amineHCID 517779—
溶媒Acetic AcidHCID 176—
生成物1-methyl-3-phenyl-4-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridin-6(7H)-oneHCID 13637652224.3%

反応条件

温度150 °C

反応手順

A mixture of 1-methyl-3-phenyl-1H-pyrazol-5-amine (1.7 g, 9.815 mmol) and 4,4,4-Trifluoro-3-oxo-butyric acid ethyl ester (2.168 g, 11.776 mmol) in acetic acid (3.0 mL) was heated at 150° C. for 10 h in a sealed tube under constant stirring. The reaction mixture was cooled to rt and poured into rapidly stirred ice-cold water to obtain the crude product as a solid. The product was collected by filtration and dried under vacuum. The product was purified by flash-chromatography (eluent: 35% EtOAc in hexane) to yield the title compound as a white solid (0.7 g, 24%). [1H-NMR (CDCl3, 300 MHz) δ 13.65 (s, 1H), 7.52-7.37 (m, 5H), 6.78 (s, 1H), 4.20 (s, 3H); LCMS RtC=1.430 min; [M+H]+=294.0]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742106B2
出典データセットuspto-grants-2014_06
ORD IDord-9ac53d9a1cf64b9fbaff364aece16c93
出典メモuspto-grants-2014_06