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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84270생성일: 2026년 10월 23일

Cesium carbonate → Ethyl 4-(4-(benzyloxy)-2-oxopyridin-1(2h)-yl)-2-methyl-2-(methylsulfonyl)butanoate

https://huagongshe.com/ko/reaction/84270

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-Benzyloxy-2(1H)-pyridoneHCID 3607724—
반응물Ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoateHCID 86670634—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-(4-(benzyloxy)-2-oxopyridin-1(2h)-yl)-2-methyl-2-(methylsulfonyl)butanoateHCID 67249611—

반응 조건

온도50 °C

반응 단계

To a solution of ethyl 4-bromo-2-methyl-2-(methylsulfonyl)butanoate (345 mg, 1.20 mmol) and 4-(benzyloxy)pyridin-2-ol (201 mg, 1.00 mmol) in tetrahydrofuran (10 mL) was added cesium carbonate (652 mg, 2.00) at ambient temperature. The resulting mixture was stirred at 50° C. overnight. The mixture was allowed to cool to ambient temperature and filtered through a celite pad. The pad was washed with ethyl acetate; the filtrates were combined and concentrated to a crude residue. The material was purified via filtration through a silica gel pad and eluted with heptanes/ethyl acetate. The desired fractions were isolated and the solvent removed via rotary evaporation affording ethyl 4-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanoate as a white solid. 302.2 mg. 1H NMR (CD3OD) 7.47, (1H, d), 7.41-7.29 (5H, m), 6.15-6.13, (1H, dd), 5.96 (1H, d), 5.07 (2H, s), 4.20-4.12 (2H, m), 4.00-3.93 (1H, m), 3.47 (1H, q), 3.21 (3H, s), 2.60-2.53 (1H, m), 2.32-2.25 (1H, M), 3.20 (3H, s), 1.26 (3H, t) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846933B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d8d41e5267d141edaefdfd8785b98bb8
출처 메모uspto-grants-2014_09