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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244319생성일: 2026년 10월 26일

Cesium fluoride → Methyl 4-amino-6-(4-chloro-3-fluorophenyl)-5-fluoropicolinate

https://huagongshe.com/reaction/244319

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물4-Chloro-3-fluorophenylboronic AcidHCID 2778656—
반응물Methyl 4-amino-6-chloro-5-fluoropicolinateHCID 86668302—
촉매HCID 178418476HCID 178418476—
생성물Methyl 4-amino-6-(4-chloro-3-fluorophenyl)-5-fluoropicolinateHCID 7049854771%

반응 조건

온도85 °C

반응 단계

Methyl 4-amino-6-chloro-5-fluoropicolinate (3.0 g, 14.66 mmol), (4-chloro-3-fluorophenyl)boronic acid (3.07 g, 17.60 mmol), bis(triphenylphosphine)palladium(II) dichloride (1.029 g, 1.466 mmol), and cesium fluoride (4.45 g, 29.3 mmol) were comined in a flask that was sealed and purged with nitrogen. Dioxane (50 ml) and Water (10.00 ml) were added and the reaction mixture was heated at 85° C. for 18 hrs. The reaction mixture was diluted with ethyl acetate and water. The organic phase was washed with saturated sodium chlride, dried over magnesium sulfate, filtered, and concentrated onto silica. The product was purified by flash chromatography (SiO2, 0-40% EtOAc:Hex gradient) to provide the title compound (3.11 g, 10.41 mmol, 71.0% yield) as a white solid: 1H NMR (400 MHz, DMSO-d6) d 3.85 (s, 3H), 6.72 (s, 2H), 7.49 (d, J=6.3 Hz, 1H), 7.68-7.80 (m, 2H), 7.84 (dd, J=10.8, 1.3 Hz, 1H); 19F NMR (376 MHz, DMSO-d6) d −144.47, −116.07; ESIMS m/z 299 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658568B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-27a9f8f056f84a8891d81a0b5c45f50b
출처 메모uspto-grants-2014_02