Réaction #2075724
ord-7c12127ebb5249b681922313eb88b2d3
Équation de réaction
Solvants
Conditions de réaction
Traitement
- 1AutreThe reactor was purged
- 2AutreThe volatiles were removed under vacuum
- 3ExtractionThe aqueous phase was extracted with an additional ethyl acetate
- 4Lavageand the combined extracts were washed with brine
- 5Autredried
- 6Autreevaporated
- 7AutreThe residue was purified by flash chromatography on silica gel (0-30% ethyl acetate gradient in hexanes)
Mode opératoire
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).