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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407211생성일: 2026년 10월 25일

1,2-Dimethoxyethane → Methyl 4-acetamido-3-(benzyloxy)-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinate

https://huagongshe.com/reaction/407211

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Cesium fluorideHCID 25953—
반응물4-Chloro-2-fluoro-3-methoxyphenylboronic acidHCID 44129706—
반응물Methyl 4-acetamido-3-(benzyloxy)-6-bromopicolinateHCID 86600141—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
생성물Methyl 4-acetamido-3-(benzyloxy)-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinateHCID 71150541—

반응 조건

온도100 °C

반응 단계

Methyl 4-acetamido-3-(benzyloxy)-6-bromopicolinate (prepared as in Kong, L. C. C. et al. U.S. Patent Application Publication 2005/0176767; 1.5 g, 4.0 mmol), (4-chloro-2-fluoro-3-methoxyphenyl)boronic acid (1.2 g, 5.9 mmol), bis(triphenylphosphine)-palladium(II) dichloride (PdCl2(PPh3)2; 278 mg, 0.4 mmol), cesium fluoride (CsF; 1.2 g, 7.9 mmol), 1,2-dimethoxyethane (DME; 7 mL), and H2O (7 mL) were combined and heated in a Biotage microwave at 100° C. for 15 min. H2O was added to the reaction mixture, and the product was extracted with EtOAc. The combined organic extracts were washed with satd aq NaCl, dried with sodium sulfate (Na2SO4), filtered and concentrated. Flash chromatography (SiO2; 0-45% EtOAc/cyclohexane gradient) afforded methyl 4-acetamido-3-(benzyloxy)-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinate as a yellow solid: mp 115-120° C.; 1H NMR (400 MHz, CDCl3) δ 8.87 (d, J=1.6 Hz, 1H), 7.66 (s, 1H), 7.59 (dd, J=8.5, 7.7 Hz, 1H), 7.45 (s, 5H), 7.24 (dd, J=8.6, 1.7 Hz, 1H), 5.13 (s, 2H), 4.03 (s, 3H), 3.99 (d, J=1.0 Hz, 3H), 1.88 (s, 3H); ESIMS m/z 459 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-e25d925e87b84e21bb3210939bf99a9a
출처 메모uspto-grants-2014_06