Reaktion #1539

ord-28a790364d3a4b39a6924f5c3d8fb5d8

Reaktionsgleichung

Cl.N=C(N)c1ccccc1.O
benzamidine hydrochloride hydrate
C[O-].[Na+]
sodium methoxide
CCOC(=O)C(CC)C(=O)OCC
diethyl ethylmalonate
CCc1c(O)nc(-c2ccccc2)[nH]c1=O
5-ethyl-6-hydroxy-2-phenyl-4(3H)-pyrimidinone
Ausbeute 51.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux for 25 h
  3. 3
    Sonstigeto remove the bulk of the methanol
  4. 4
    workup.ADDITIONThe residue was diluted with 300 mL of water
  5. 5
    FiltrationThe solid precipitate was collected by filtration
  6. 6
    Sonstigedried under vacuum at 50° C.

Vorschrift

A mixture of 45.19 g (0.29 mol) of benzamidine hydrochloride hydrate, 127.42 g (0.59 mol) of 25% sodium methoxide in methanol, 55 mL (0.29 mol) of diethyl ethylmalonate and 175 mL of methanol was heated at reflux for 25 h. The mixture was rotovapped to remove the bulk of the methanol. The residue was diluted with 300 mL of water and the pH was adjusted to 7 with concentrated hydrochloric acid. The solid precipitate was collected by filtration and dried under vacuum at 50° C. to afford 31.89 g (51%) of crude 5-ethyl-6-hydroxy-2-phenyl-4(3H)-pyrimidinone as a pale yellow solid. 1H-NMR (d6-DMSO) δ 1.05(3H,t), 2.39(2H,q), 7.5(3H,m), 8.1(2H,m).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726124uspto-grants-1998_03