Reacción #2358549

ord-f76c8111170147f79d0beeec24f7cc12

Ecuación de reacción

COCOc1cc(OCc2ccccc2)c(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)cc1C(C)C
compound ( 4 )
COCOc1cc(OCc2ccccc2)c(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)cc1C(C)C
5-(2-(benzyloxy)-5-isopropyl-4-(methoxymethoxy)phenyl)-4-(6-morpholinopyridin-3-yl)-4H-1,2,4-triazol-3-ol
Cl
HCl
CC(C)c1cc(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)c(OCc2ccccc2)cc1O.Cl
5-(2-(benzyloxy)-4-hydroxy-5-isopropylphenyl)-4-(6-morpholinopyridin-3-yl)-4H-1,2,4-triazol-3-ol hydrochloride
Rendimiento 74.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled
  2. 2
    OtroThe white precipitate thus obtained
  3. 3
    Filtraciónwas filtered
  4. 4
    Lavadowashed with ether (2×20 ml)

Procedimiento

To the solution of compound (4) (2.10 g, 3.95 mmol) in MeOH (100 ml), HCl (2 ml, 2N) was added, and then the resultant mixture was heated at 65° C. for 5 h, then cooled. The white precipitate thus obtained was filtered, washed with ether (2×20 ml) gave 1.53 g (74%) of 5-(2-(benzyloxy)-4-hydroxy-5-isopropylphenyl)-4-(6-morpholinopyridin-3-yl)-4H-1,2,4-triazol-3-ol hydrochloride (5).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09120745B2uspto-grants-2015_09