Reacción #1545

ord-475d4575be964743a02cc9754560986f

Ecuación de reacción

CCc1cc(=O)[nH]c(-c2ccccc2)n1
6-ethyl-2-phenyl-4(3H)-pyrimidinone
O=C1CCC(=O)N1Cl
N-chlorosuccinimide
CCc1nc(-c2ccccc2)[nH]c(=O)c1Cl
5-chloro-6-ethyl-2-phenyl-4(3H)-pyrimidinone
Rendimiento 87.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was cooled
  2. 2
    workup.ADDITIONpoured
  3. 3
    Otroonto crushed ice
  4. 4
    FiltraciónThe mixture was filtered
  5. 5
    Otrothe solid collected
  6. 6
    Lavadowas washed with water
  7. 7
    SecadoThe solid was dried in a vacuum oven at 50C

Procedimiento

A stirred solution of 7.81 g (39.1 mmol) of 6-ethyl-2-phenyl-4(3H)-pyrimidinone and 5.80 g (43.4 mmol) of N-chlorosuccinimide in 100 mL of glacial acetic acid was heated at 90° C. for 4 h. The mixture was cooled, poured onto crushed ice and allowed to stand until the ice had melted. The mixture was filtered and the solid collected was washed with water and a little ether. The solid was dried in a vacuum oven at 50C to afford 7.99 g of 5-chloro-6-ethyl-2-phenyl-4(3H)-pyrimidinone (an intermediate for compound 172) as a white solid. 1H-NMR (d6-DMSO) 1.30(3H,t), 2.8(2H,q), 7.6(3H,m), 8.2(2H.m).

Fuente

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