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HRID 448560作成日:2026年10月26日

Sodium hydride → Tert-butyl 4-((6-(5-(methylsulfonyl)indolin-1-yl)pyrimidin-4-yl)oxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/448560

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5-(Methanesulfonyl)-2,3-dihydro-1H-indoleHCID 2736136—
反応物tert-Butyl 4-[(6-chloropyrimidin-4-yl)oxy]piperidine-1-carboxylateHCID 21906116—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物Tert-butyl 4-((6-(5-(methylsulfonyl)indolin-1-yl)pyrimidin-4-yl)oxy)piperidine-1-carboxylateHCID 2524241440.3%

反応手順

To a suspension of sodium hydride (0.25 g, 2 eq) in 10 mL of DMF, was added 5-methanesulfonyl-2,3-dihydro-1H-indole (0.63 g, 1 eq). The mixture was stirred at room temperature for 10 minutes then 3a (1 g, 3.19 mmol) was added. The resulting mixture was heated up to 80° C. for 18 h. The reaction mixture was then allowed to cool down to room temperature and brine (200 mL) was added. The solution was extracted with DCM twice (200 mL then 50 mL). The combined extracts were washed with brine (2×50 mL), dried over magnesium sulfate and filtered. The solvent was removed under vacuum to give an oil which was purified by column chromatography (elution with 10-100% ethyl acetate and 0.1% TEA in hexanes) to give 0.61 g of 4a (40% yield), LCMS 475.2 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481731B2
出典データセットuspto-grants-2013_07
ORD IDord-a6d2503a08774c0e9f7736b2e59ee886
出典メモuspto-grants-2013_07