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HRID 2252作成日:2026年10月23日

Potassium hydride → 4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene

https://huagongshe.com/ja/reaction/2252

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium hydrideHCID 82127—
反応物1-Bromo-4-phenylmethoxybenzeneHCID 138835—
反応物4-(Pyridin-4-YL)piperazin-2-oneHCID 18918356—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物AmmoniaHCID 222—
生成物4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzeneHCID 54227295123.3%

反応手順

To a stirred suspension of 4-(4-pyridyl) piperazin-2-one (880 mg) in dimethyl formamide (20 ml) was added potassium hydride (1.0 ml of a 20% dispersion) and the mixture stirred for 0.5 hr, after which time was added copper (I) iodide (1.0 g). After 0.25 hr there was added 4-benzyloxybromobenzene (1.2 g) and the mixture stirred at 140° C. in an argon atmosphere for 2 hr. The reaction mixture was diluted with water and brine and extracted with dichloromethane (3×40 ml); the combined extracts were washed with water and brine, dried (PS paper) and evaporated to give crude product as a pasty solid (2.0 g). This was purified by flash chromatography on silica, eluting with dichloromethane/methanol/conc. ammonia (97:2.5:0.5 v/v) to give 4-benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene as a colourless solid (1.1 g) NMR δ (d6DMSO): 3.7-3.9 (4H,m); 4.1 (2H,s); 5.1 (2H,s); 6.85 (2H,d); 7.05 (2H,d); 7.25 (2H,d); 7.3-7.6 (5H,m); 8.2 (2H,d); m/e 360 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728701
出典データセットuspto-grants-1998_03
ORD IDord-35c0a06e7c3d4c9f82f5835490d4df81
出典メモuspto-grants-1998_03