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HRID 1518460作成日:2026年10月26日

Trimethylsilyl iodide → 1-(4-(methylthio)phenyl)-4-(piperidin-4-yloxy)pyridin-2(1H)-one

https://huagongshe.com/reaction/1518460

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethylsilyl iodideHCID 85247—
反応物Benzyl 4-(1-(4-(methylthio)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylateHCID 67368480—
溶媒DichloromethaneHCID 6344—
生成物1-(4-(methylthio)phenyl)-4-(piperidin-4-yloxy)pyridin-2(1H)-oneHCID 6736870873.3%

反応手順

To a stirring solution of benzyl 4-(1-(4-(methylthio)phenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate (367 mg, 0.815 mmol) in CH2Cl2 (5 mL) at 0° C. was added iodotrimethylsilane (0.33 mL, 2.4 mmol, Aldrich). The reaction was stirred for 40 min and then quenched at 0° C. with HCl (1N in H2O, 5 mL). To the resulting mixture was diluted with CH2Cl2 and extracted with H2O. The H2O layer was basified with NaOH (1N in H2O, 10 mL) and extracted with CH2Cl2 (2×). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo to yield 189 mg crude product as an off-white solid. MS (ESI) 317 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08232404B2
出典データセットuspto-grants-2012_07
ORD IDord-df8812161fcc461fa46a9d368fb065ce
出典メモuspto-grants-2012_07