Réaction #2075724

ord-7c12127ebb5249b681922313eb88b2d3

Équation de réaction

COc1c(N)nc(Cl)nc1Cl
2,6-Dichloro-5-methoxypyrimidin-4-ylamine
CC(=O)[O-].[Na+]
sodium acetate
c1ccc(P(CCCCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1
DPPB
CCOC(=O)c1nc(Cl)nc(N)c1OC
title compound
CCOC(=O)c1nc(Cl)nc(N)c1OC
6-Amino-2-chloro-5-methoxypyrimidine-4-carboxylic acid ethyl ester

Solvants

Conditions de réaction

Température
110°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reactor was purged
  2. 2
    AutreThe volatiles were removed under vacuum
  3. 3
    ExtractionThe aqueous phase was extracted with an additional ethyl acetate
  4. 4
    Lavageand the combined extracts were washed with brine
  5. 5
    Autredried
  6. 6
    Autreevaporated
  7. 7
    AutreThe 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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07642220B2uspto-grants-2010_01