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HRID 389974作成日:2026年10月26日

Tetrahydrofuran → [4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanone

https://huagongshe.com/reaction/389974

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物[4-(6-Nitropyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanoneHCID 39235237—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物[4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanoneHCID 6741914549%

反応条件

温度25 °C

反応手順

To a solution of [4-(6-nitropyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.089 g, 0.23 mmol) in 1:1 THF:MeOH (5 mL) was added 10% Pd/C (0.051 g). The resulting mixture was stirred under hydrogen atmosphere at 25° C. for 4 h. After filtering through a celite cake, the solution was concentrated in vacuo and yielded the title compound as a light yellow solid (0.039 g, 49% yield). MS (ES+) m/z 351.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383628B2
出典データセットuspto-grants-2013_02
ORD IDord-0486ccf4f3a8436299ae344700d3b835
出典メモuspto-grants-2013_02