Reaktion #7730

ord-083c6a63c5cf4ef4a1d50b8a2e104444

Reaktionsgleichung

CCOC(=O)CC(=O)C(OCC)OCC
4,4-diethoxy-3-oxo-butyric acid ethyl ester
N=C(N)N.O=C(O)O
guanidine carbonate
CCOC(OCC)c1cc(=O)[nH]c(N)n1
2-Amino-6-diethoxymethyl-3H-pyrimidin-4-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux until no solid
  2. 2
    Sonstige(˜4 hours)
  3. 3
    EinengenThe mixture was concentrated
  4. 4
    workup.ADDITIONdiluted with water
  5. 5
    Filtrationthe solid was collected by filtration
  6. 6
    Sonstigeto give D1.1 (13.1 g, 74%) as a beige solid

Vorschrift

A solution of 4,4-diethoxy-3-oxo-butyric acid ethyl ester [Johnson, T. B. and Mikeska, L. A. J. Am. Chem. Soc. 41, 810 (1919)] (18.0 g, 82.5 mol) in ethanol (300 mL) was treated with guanidine carbonate (14.8 g, 82.5 mol) and this was stirred under reflux until no solid remained (˜4 hours). The mixture was concentrated, diluted with water and the solid was collected by filtration to give D1.1 (13.1 g, 74%) as a beige solid. 1H-NMR (DMSO-d6) δ: 10.78 (1H, br s), 6.61 (2H, br s), 5.63 (1H, s), 4.90 (1H, s), 3.51 (4H, m), 1.13 (6H, t, J=7.1 Hz). LC/MSc: ret. time: 0.757 min. (M+H)+: 214. M.p.: 198.0–202.7° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087614B2uspto-grants-2006_08