Reacción #1539

ord-28a790364d3a4b39a6924f5c3d8fb5d8

Ecuación de reacción

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
Rendimiento 51.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaat reflux for 25 h
  3. 3
    Otroto remove the bulk of the methanol
  4. 4
    workup.ADDITIONThe residue was diluted with 300 mL of water
  5. 5
    FiltraciónThe solid precipitate was collected by filtration
  6. 6
    Otrodried under vacuum at 50° C.

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726124uspto-grants-1998_03