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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42724생성일: 2026년 10월 25일

Water → Bms-777607

https://huagongshe.com/reaction/42724

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물Iodo benzene diacetateHCID 12217721—
반응물3-Chloro-4-(4-(4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamido)-2-fluorophenoxy)picolinamideHCID 25231978—
용매Ethyl AcetateHCID 8857—
생성물Bms-777607HCID 2479441874%

반응 단계

To 3-chloro-4-(4-(4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamido)-2-fluorophenoxy)picolinamide (1.2 g, 2.1 mmol) in ethyl acetate (16 mL), acetonitrile (16 mL), and water (8 mL) at 0° C. was added iodobenzene diacetate (820 mg, 2.6 mmol, Aldrich). After stirring at rt for 2 h, the reaction was filtered to collect the crude product. The solid was washed with additional ethyl acetate. The filtrate was washed with saturated aqueous sodium bicarbonate solution and the organic phase was dried over anhydrous sodium sulfate and concentrated in vacuo. The precipitate and filtrate were combined and purified by flash chromatography on silica gel (2% methanol/chloroform) to give the title compound (810 mg, 74%) as a white solid. 1H NMR (DMSO-d6) δ 10.57 (s, 1H), 7.83-7.79 (m, 2H), 7.67 (d, 1H, J=5.6 Hz), 7.41-7.38 (m, 3H), 7.36-7.22 (m, 3H), 6.44 (d, 1H, J=7.6 Hz), 6.36 (br s, 2H), 5.86 (d, 1H, J=6.0 Hz), 4.18 (q, 2H, J=7.2 Hz), 1.23 (t, 3H, J=7.2 Hz); MS(ESI+) m/z 513.09 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536200B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-271eb0c4e7fe42b0bde8c2e4c11af705
출처 메모uspto-grants-2013_09