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HRID 389978作成日:2026年10月26日

1-Hexanesulfonyl chloride → Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amide

https://huagongshe.com/reaction/389978

反応式

関与物質

役割名称HCID仕込み量
反応物1-Hexanesulfonyl chlorideHCID 84504—
反応物[4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanoneHCID 67419145—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amideHCID 112949618%

反応条件

温度60 °C

反応手順

To a solution of [4-(6-aminopyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.035 g, 0.10 mmol) in pyridine (3 mL) was added hexanesulfonyl chloride (0.022 mL, 0.12 mmol). After heating at 60° C. for 20 h, the mixture was diluted with ethyl acetate (100 mL), washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. Purification by preparative thin layer chromatography afforded the title compound as a white solid (3.8 mg, 8% yield). 1H NMR (300 MHz, CDCl3) δ 7.66, 7.29, 4.08, 3.91, 3.38, 3.27, 3.08, 1.84, 1.35, 1.27, 0.87. MS (ES+) m/z 499.4 (M+1).

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-e33776045e6c44e9acbd26e6e6c5ac00
出典メモuspto-grants-2013_02