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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384696생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/384696

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물tert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
반응물2-Chloro-5-iodopyridin-4-amineHCID 45480366—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(((2-chloro-5-iodopyridin-4-yl)amino)methyl)piperidine-1-carboxylateHCID 5961338946%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367658B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-5d36f32fe1da480b9bdffd7e3691fc9a
출처 메모uspto-grants-2013_02