1,2-Dichloroethane → HCID 58179455, Verbindung

Temperatur

0 °C

To a solution of 2-fluoropyridine-3-carboxylic acid (1.41 g, 10.00 mmol) in anhydrous DMF (15 mL) was added HOBT (2.56 g, 16.74 mmol) and Et3N (2.0 g, 20.09 mmol) at RT. The mixture was cooled to 0° C., treated with a solution of N4-(2,3-difluorophenyl)pyridine-3,4-diamine in DMF (15 mL), stirred for 15 min at RT and EDC (3.2 g, 16.74 mmol) was added portion wise. The reaction mixture was warmed to RT and stirred for 16 hr. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (4×200 mL). The combined organics were washed with saturated aq. NaHCO3 solution (2×100 mL), water (2×100 mL), brine solution (100 mL), and dried (Na2SO4). Filtration and evaporation of the solvent in vacuo gave a brown solid. Chromatographic purification (silica gel, 1% methanol in chloroform) provided N-(4-(2,3-difluorophenylamino)pyridin-3-yl)-2-fluoropyridine-3-carboxamide (1.05 g, 45% yield) as yellow solid; LC-MS: 345.2 (M+H).

1. temperatureThe reaction mixture was warmed to RT
2. stirringstirred for 16 hr
3. extractionextracted with EtOAc (4×200 mL)
4. washThe combined organics were washed with saturated aq. NaHCO3 solution (2×100 mL), water (2×100 mL), brine solution (100 mL)
5. dry with materialdried (Na2SO4)
6. filtrationFiltration and evaporation of the solvent in vacuo
7. customgave a brown solid
8. customChromatographic purification (silica gel, 1% methanol in chloroform)

ORD-Eintrag

ord-a5a4444d8fa44a67bc00ec62301270f6

Quelldatensatz

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07872031B2