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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468650생성일: 2026년 10월 25일

Cesium carbonate → Ethyl (2R)-4-(3,5-difluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoate

https://huagongshe.com/reaction/468650

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물3,5-difluoro-4-iodopyridin-2(1H)-oneHCID 70665196—
반응물(R)-ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoateHCID 86670635—
용매Tert-butanol tetrahydrofuranHCID 66775918—
생성물Ethyl (2R)-4-(3,5-difluoro-4-iodo-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)butanoateHCID 8667065432%

반응 단계

Cesium carbonate (1.90 g, 5.84 mmol) was added to a solution of the 3,5-difluoro-4-iodopyridin-2(1H)-one (1.0 g, 3.9 mmol) and ethyl (2R)-4-bromo-2-methyl-2-(methylsulfonyl)butanoate, T1, (1.45 g, 5.06 mmol) in tetrahydrofuran:t-butanol (1:1, 50 mL). The resulting suspension was heated to reflux and was stirred at this temperature for 72 h. The reaction was filtered through celite, and the filter pad was washed with EtOAc (3×50 mL). The combined filtrates were concentrated and the crude product was purified via flash chromatography on an Analogix SF15-24 g column using an eluent of EtOAc in hexanes (0-50%) to afford the title compound as a yellow solid (575.6 mg, 32%). MS (LCMS) m/z 463.9 (M+1). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.23 (s, 3H) 1.58 (s, 3H) 2.20 (dt, J=13.90, 7.00 Hz, 1H) 2.52-2.62 (m, 1H) 3.14 (s, 3H) 4.00 (t, J=7.61 Hz, 2H) 4.05-4.22 (m, 2H) 7.94 (dd, J=4.20, 2.05 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08624034B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-7d252824ca624984a0d3279a86c7e6d6
출처 메모uspto-grants-2014_01