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HRID 448560생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/448560

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물5-(Methanesulfonyl)-2,3-dihydro-1H-indoleHCID 2736136—
반응물tert-Butyl 4-[(6-chloropyrimidin-4-yl)oxy]piperidine-1-carboxylateHCID 21906116—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물Tert-butyl 4-((6-(5-(methylsulfonyl)indolin-1-yl)pyrimidin-4-yl)oxy)piperidine-1-carboxylateHCID 2524241440.3%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481731B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-a6d2503a08774c0e9f7736b2e59ee886
출처 메모uspto-grants-2013_07