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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2,6-Difluorobenzeneboronic acid, pinacol ester | HCID 44717719 | — |
| Edukt | Methyl 3-amino-6-bromo-5-fluoropicolinate | HCID 72698878 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Produkt | Methyl 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinate | HCID 59226608 | 74,4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09200004B2 |
|---|
| Quelldatensatz | uspto-grants-2015_12 |
|---|
| ORD ID | ord-fe373c2017ba4db18de1332bab3cdb25 |
|---|
| Quellennotiz | uspto-grants-2015_12 |
|---|