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HRID 384696作成日:2026年10月26日

Water → Tert-butyl 4-(((2-chloro-5-iodopyridin-4-yl)amino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/384696

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物tert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
反応物2-Chloro-5-iodopyridin-4-amineHCID 45480366—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(((2-chloro-5-iodopyridin-4-yl)amino)methyl)piperidine-1-carboxylateHCID 5961338946%

反応手順

NaH (0.098 g, 3.9 mmol) was added to a solution of 2-chloro-5-iodopyridin-4-amine (0.500 g, 1.96 mmol) in DMF (12 mL) and the mixture was stirred for 30 min at r.t. The temperature was then raised to 80° C. and a solution of tert-butyl 4-(bromomethyl)-piperidine-1-carboxylate (1.093 g, 3.93 mmol) in DMF (2 mL) was added. The reaction mixture was stirred at 80° C. for 2 h, then cooled to r.t. NaH (0.050 g, 2.00 mmol) was added and the reaction mixture was heated for 1 h at 80° C. After cooling, water (40 mL) was added and the reaction mixture was partitioned between ethyl acetate and aq. NaHCO3. The organic phase was washed with brine, dried (MgSO4) and concentrated. The crude product was purified by flash silica chromatography, eluting with ethyl acetate and hexane (1/9), to give the title compound as a pink solid (0.405 g, 46%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367658B2
出典データセットuspto-grants-2013_02
ORD IDord-5d36f32fe1da480b9bdffd7e3691fc9a
出典メモuspto-grants-2013_02