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HRID 448582作成日:2026年10月26日

Sodium hydride → 4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/448582

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)amino]piperidine-1-carboxylateHCID 22309472—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 5807412562.1%

反応手順

To a solution of NaH (0.62 g, 15.5 mmol, 60% NaH) in 40 mL of DMF, 5-methanesulfonyl-2,3-dihydro-1H-indole (1.9 g, 9.63 mmol) was added and the mixture was stirred at room temperature for 30 minutes. 17a (3.09 g, 9.88 mmol) was added in DMF and the mixture was heated at 85° C. for 17 h. After cooling to room temperature, brine was added (200 mL) and the mixture was extracted with DCM (200 mL then 3×500 mL). The combined extracts were washed with brine (3×100 mL), dried, filtered and evaporated. The residue was purified by flash chromatography (eluent: 25 to 100% EtOAc in hexane with 0.1% triethylamine) to afford 2.83 g (62%) of 17b.

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-193c47e56d1b44f9927c0f14fe6990bf
出典メモuspto-grants-2013_07