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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1499434Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1499434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2,6-Difluorobenzeneboronic acid, pinacol esterHCID 44717719—
EduktMethyl 3-amino-6-bromo-5-fluoropicolinateHCID 72698878—
KatalysatorHCID 178418851HCID 178418851—
ProduktMethyl 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinateHCID 5922660874,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09200004B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-fe373c2017ba4db18de1332bab3cdb25
Quellennotizuspto-grants-2015_12