Reacción #1540

ord-2b0378d7412b4bedb3ed0ed2242b2a38

Ecuación de reacción

Cl.N=C(N)c1ccccc1.O
benzamidine hydrochloride hydrate
CC(=O)[O-].[Na+]
sodium acetate
CCOC(=O)C=C(OCC)OCC
ethyl 3,3-diethoxyacrylate
CS(C)=O
DMSO
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
Rendimiento 57.0%

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was cooled
  2. 2
    Lavadowashed with two 100 mL portions of ether
  3. 3
    Filtraciónthe precipitate was collected by filtration
  4. 4
    Otrodried under vacuum at 50° C.

Procedimiento

A mixture of 3.14 g (20.0 mmol) of benzamidine hydrochloride hydrate, 1.65 g (20.1 mmol) of powdered anhydrous sodium acetate, 4.17 g (22.2 mmol) of ethyl 3,3-diethoxyacrylate and 10 mL of DMSO was heated at 120° C. for 8 h. The mixture was cooled, diluted with 50 mL of 5% aqueous NaOH and washed with two 100 mL portions of ether. The aqueous layer was acidified with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum at 50° C. to furnish 2.28 g (57%) of crude 6-ethoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid 1 H-NMR (d6-DMSO) δ 1.35(3H,t), 4.33(2H,q), 5.60(1H,s), 7.50(3H,m), 8.2(2H,m).

Fuente

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