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HRID 1499434作成日:2026年10月25日

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

https://huagongshe.com/reaction/1499434

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2,6-Difluorobenzeneboronic acid, pinacol esterHCID 44717719—
反応物Methyl 3-amino-6-bromo-5-fluoropicolinateHCID 72698878—
触媒HCID 178418851HCID 178418851—
生成物Methyl 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinateHCID 5922660874.4%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09200004B2
出典データセットuspto-grants-2015_12
ORD IDord-fe373c2017ba4db18de1332bab3cdb25
出典メモuspto-grants-2015_12