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HRID 270895作成日:2026年10月26日

Dimethylformamide → 1-{2-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/270895

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物ethyl 1H-pyrazole-4-carboxylateHCID 142179—
反応物1-(Chloroacetyl)-4-(4-fluorophenyl)piperazineHCID 1848511—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物1-{2-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-1H-pyrazole-4-carboxylic acid ethyl esterHCID 58778026—

反応手順

Protocol T was followed using 1H-Pyrazole-4-carboxylic acid ethyl ester, K2CO3, 2-Chloro-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1/1) afforded the title compound as a white solid. 1H NMR (400 MHz, CDCl3): 8.2 (s, 1H), 7.92 (s, 1H), 6.94-7.0 (m, 2H), 6.82-6.88 (m, 2H), 5.0 (s, 2H), 4.1-4.2 (q, 2H), 3.74-3.82 (t, 2H), 3.62-3.72 (t, 2H), 3.0-3.12 (m, 4H), 1.28-1.42 (t, 3H). MS (ES) M+H expected 360.39, found 361.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449576B1
出典データセットuspto-grants-2008_11
ORD IDord-dea9268ffbdd4612bd15068595c97724
出典メモuspto-grants-2008_11