Reacción #2304

ord-9f122af1a0394a17b79d34afbf18a558

Ecuación de reacción

COc1ccc(N2CCN(c3ccncc3)CC2)cc1
product
COc1ccc(N2CCN(c3ccncc3)CC2)cc1
4-[4-(4-pyridyl)-piperazin-1-yl]anisole
O
water
N
ammonia
Oc1ccc(N2CCN(c3ccncc3)CC2)cc1
4-[4-(4-pyridyl)piperazin-1-yl]phenol
Rendimiento 95.6%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe solution was cooled
  2. 2
    FiltraciónThe precipitate was filtered
  3. 3
    Lavadowashed with water
  4. 4
    Otrodried

Procedimiento

The product from step (i) (1.5 g) in concentrated hydrobromic acid (30 ml) was heated under argon at 130°-135° C. for 21/2 hours. The solution was cooled, poured into water (150 ml) and basified with aqueous ammonia. The precipitate was filtered, washed with water and dried to give 4-[4-(4-pyridyl)piperazin-1-yl]phenol (1.36 g) as a solid: m.p. 310°-312° C.; NMR(d6DMSO) δ 8.2(2H,d); 6.8(4H,m); 6.66(2H,d); 3.45(4H,m); 3.08(4H,m).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728701uspto-grants-1998_03