戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 83646作成日:2026年10月23日

Sodium hydride → HCID 66571463、化合物

https://huagongshe.com/ja/reaction/83646

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
反応物N-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamideHCID 66571403—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 66571463HCID 66571463—

反応条件

温度70 °C

反応手順

N-benzyl-1-(1H-indole-2-carbonyl)-N-methylpiperidine-4-carboxamide (50 mg, 0.133 mmol) dissolved in 0.5 mL of DMF was added to a suspension of sodium hydride (7.99 mg, 0.200 mmol) in 1.0 mL of DMF. The reaction was heated at 70° C. for ten minutes before adding 2-methoxyethyl 4-methylbenzenesulfonate (0.144 mL, 0.266 mmol). The reaction was allowed to stir overnight. After 18 hours, the reaction was cooled to room temperature before diluting with water and ethyl acetate. The organic phase was washed with water followed by saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated. The crude material was purified via column chromatography using 50-80% ethyl acetate/hexanes. The purification provided product as a white solid 1H-NMR (400 MHz, DMSO-d6) 7.63-7.49, 7.43-7.14, 7.12-7.03, 6.67-6.58, 4.68, 4.63-4.06, 3.53, 3.20-3.13, 3.10-2.92, 2.79, 1.92-1.50

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846684B2
出典データセットuspto-grants-2014_09
ORD IDord-d3af2161ee3b470897c7471e4f176c77
出典メモuspto-grants-2014_09