戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2263204作成日:2026年10月27日

Water → 4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]-N-pyrazin-2-ylpiperazine-1-carboxamide

https://huagongshe.com/reaction/2263204

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物1-[4-(4-Fluorophenyl)-2-thiazolyl]piperazineHCID 8027201—
反応物2,2,2-Trichloroethyl pyrazin-2-ylcarbamateHCID 68777403—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]-N-pyrazin-2-ylpiperazine-1-carboxamideHCID 6877909834.1%

反応手順

A mixture if 2,2,2-trichloroethyl pyrazin-2-ylcarbamate (226 mg, 0.835 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperazine (200 mg, 0.760 mmol) and diisopropylethylamine (0.265 ml, 1.52 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 3 days. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was wash washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified silica gel column chromatography (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (99.7 mg, 34.0%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07851473B2
出典データセットuspto-grants-2010_12
ORD IDord-996151c7ada64869bae11e6fd38fd5fa
出典メモuspto-grants-2010_12