戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 10776作成日:2026年10月25日

3-Fluoro-4-(4-methylpiperazin-1-yl)aniline → 1-(2-Fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/10776

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluoro-4-(4-methylpiperazin-1-yl)anilineHCID 2783055—
反応物Thiocarbonyl diimidazoleHCID 11412697—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Fluoro-4-isothio-cyanatophenyl)-4-methylpiperazineHCID 9942978—

反応手順

Thiocarbonyl diimidazole (3.00 g, 3.53 mmol) (Aldrich) was dissolved in N,N-dimethylformamide (10 mL) and the solution was cooled to −10° C. (ice/acetone bath). A solution of 3-fluoro-4-(4-methyl-1-piperazinyl) benzenamine (2.26 g, 10.8 mmol) (from Step B above) in N,N-dimethylformamide (30 mL) was added over a period of 30 minutes, then the cooling bath was removed and the solution was stirred overnight. Ice-water was then added (100 mL) and the mixture was extracted with ether (3×200 mL). The combined ether layers were dried (MgSO4), filtered, and evaporated to give 1-(2-fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine as a yellow oil that solidified on standing (3.88 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094896B2
出典データセットuspto-grants-2006_08
ORD IDord-8e88da186bb64330afe884ecd3c3eb32
出典メモuspto-grants-2006_08