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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1499434생성일: 2026년 10월 27일

Diisopropylethylamine → Methyl 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinate

https://huagongshe.com/reaction/1499434

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2,6-Difluorobenzeneboronic acid, pinacol esterHCID 44717719—
반응물Methyl 3-amino-6-bromo-5-fluoropicolinateHCID 72698878—
촉매HCID 178418851HCID 178418851—
생성물Methyl 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinateHCID 5922660874.4%

반응 조건

온도100 °C

반응 단계

To a screw-cap vial equipped with a magnetic stir bar, methyl 3-amino-6-bromo-5-fluoropyridine-2-carboxylate (99.6 mg, 0.400 mmol) was added, followed by 2-(2,6-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (Combi-Blocks, 190 mg, 0.80 mmol), and bis(tri-tert-butylphosphine)palladium (40.9 mg, 0.080 mmol). The vial was sealed with a PTFE-lined septum, evacuated and backfilled with nitrogen three times. 1,4-Dioxane (2.0 mL) was added via a syringe, followed by DIPEA (0.14 mL, 0.80 mmol) and deoxygenated water (0.05 mL). The mixture was heated at 100° C. for 2 h. After cooling to room temperature, the mixture was diluted with EtOAc (40 mL) and washed with water (40 mL) and brine (40 mL), then dried over Na2SO4, and concentrated under reduced pressure. The resulting residue was purified by chromatography on silica gel (0-50% EtOAc in hexanes) to give the sub-title compound as a white solid (84.0 mg, 74%). LCMS calc. for C13H10F3N2O2(M+H)+: m/z=283.1. found 283.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09200004B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-fe373c2017ba4db18de1332bab3cdb25
출처 메모uspto-grants-2015_12