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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407237생성일: 2026년 10월 24일

Potassium Fluoride → Methyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinate

https://huagongshe.com/ko/reaction/407237

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물2-(4-Chlorophenyl)-1,3,2-dioxaborinaneHCID 3468957—
반응물Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
반응물Methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinateHCID 86675409—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물Methyl 4-amino-6-(4-chlorophenyl)-5-fluoro-3-methoxypicolinateHCID 7115069672.2%

반응 조건

온도150 °C

반응 단계

To a solution of methyl 4-amino-6-chloro-5-fluoro-3-methoxypicolinate (200 mg, 0.852 mmol) in CH3CN (1.246 mL) and H2O (1.246 mL) were added 2-(4-chlorophenyl)-1,3,2-dioxaborinane (251 mg, 1.279 mmol), KF (149 mg, 2.56 mmol), palladium(II) acetate (Pd(OAc)2; 19.14 mg, 0.085 mmol), and triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt (100 mg, 0.170 mmol). The reaction mixture was then heated in a bench top Biotage microwave at 150° C. for 5 min. The reaction mixture was diluted with CH2Cl2 and washed with H2O. The organic layer was separated, dried over MgSO4, filtered and concentrated. The crude residue was purified by normal phase chromatography (eluting with 10% EtOAc/40% CH2Cl2/50% hexanes) to afford the title compound as a tan solid (191 mg, 72.1%): mp 93-94° C.; 1H NMR (400 MHz, acetone-d6) δ 7.96 (dd, J=8.8, 1.4 Hz, 2H), 7.57-7.49 (m, 2H), 5.93 (s, 2H), 3.92 (s, 3H), 3.91 (s, 3H), ESIMS m/z 311 ([M+H]+), 309 ([M−H]−).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-9c18d074a7144da5a2d778269b02827d
출처 메모uspto-grants-2014_06