Reaktion #2075724
ord-7c12127ebb5249b681922313eb88b2d3
Reaktionsgleichung
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeThe reactor was purged
- 2SonstigeThe volatiles were removed under vacuum
- 3ExtraktionThe aqueous phase was extracted with an additional ethyl acetate
- 4Waschenand the combined extracts were washed with brine
- 5Sonstigedried
- 6Sonstigeevaporated
- 7SonstigeThe residue was purified by flash chromatography on silica gel (0-30% ethyl acetate gradient in hexanes)
Vorschrift
2,6-Dichloro-5-methoxypyrimidin-4-ylamine (5.0 g, 26 mmol) was combined in 75 mL absolute ethanol with sodium acetate (2.1 g, 26 mmol), palladium acetate (280 mg, 0.91 mmol) and DPPB (1.1 g, 2.6 mmol) in a 300 mL stirred pressure reactor. The reactor was purged and pressurized to 300 psi with carbon monoxide, and heated at 110° C. for 7 h. The volatiles were removed under vacuum and the residue was taken up in ethyl acetate and water. The aqueous phase was extracted with an additional ethyl acetate; and the combined extracts were washed with brine, dried and evaporated. The residue was purified by flash chromatography on silica gel (0-30% ethyl acetate gradient in hexanes) to give the title compound (1.4 g, 23% yield): mp 118-119° C. 1H NMR (CDCl3) δ 6.18 (br s, 2H), 4.45 (q, 2H), 3.91 (s, 3H), 1.42 (t, 3H).