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HRID 1836338作成日:2026年10月26日

Sodium Iodide → 4-(4-Bromophenylsulphonyl)-1-[2-(2,4-difluorophenyl)ethyl]piperidine

https://huagongshe.com/reaction/1836338

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物4-(4-Bromobenzenesulfonyl)piperidineHCID 2761070—
反応物2,4-Difluorophenethyl bromideHCID 11298989—
溶媒AcetonitrileHCID 6342—
生成物4-(4-Bromophenylsulphonyl)-1-[2-(2,4-difluorophenyl)ethyl]piperidineHCID 1104851258.5%

反応手順

A mixture of 4-(4-bromophenylsulphonyl)piperidine (7.6 g, 0.025 mol), 2,4-difluorophenethyl bromide (8.3 g, 0.38 mol), potassium carbonate (7.5 g, 0.054 mol) and sodium iodide (5.6 g, 0.037 mol) in CH3CN (70 ml) was heated at reflux under nitrogen for 18 h. The reaction mixture was then concentrated and partitioned between water and EtOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Trituration with hexane gave 6.5 g of product as a colourless solid. δH (360 MHz, CDCl3) 1.55-1.75 (2H, m), 1.95-2.05 (4H, m), 2.45-2.55 (2H, m), 2.70-2.75 (2H, m), 2.85-2.95 (1H, m), 3.05-3.10 (2H, m), 6.70-6.85 (2H, m), 7.10-7.15 (1H, m), 7.72 (4H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06777430B2
出典データセットuspto-grants-2004_08
ORD IDord-f24e819cbe4249689051c30370095566
出典メモuspto-grants-2004_08