Réaction #2358550

ord-21b0ee9d02e64686b2e781fe48708e36

Équation de réaction

CC(C)c1cc(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)c(OCc2ccccc2)cc1OP(=O)(OCc1ccccc1)OCc1ccccc1
Mixture ( 6 )
CC(C)c1cc(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)c(OCc2ccccc2)cc1OP(=O)(OCc1ccccc1)OCc1ccccc1
dibenzyl 5-(benzyloxy)-4-(5-hydroxy-4-(6-morpholinopyridin-3-yl)-4H-1,2,4-triazol-3-yl)-2-isopropylphenyl phosphate
CC(C)c1cc(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)c(O)cc1OP(=O)(O)O
Compound 2
Rendement 81.0%
CC(C)c1cc(-c2nnc(O)n2-c2ccc(N3CCOCC3)nc2)c(O)cc1OP(=O)(O)O
5-hydroxy-4-(5-hydroxy-4-(6-morpholinopyridin-3-yl)-4H-1,2,4-triazol-3-yl)-2-isopropylphenyl dihydrogen phosphate
Rendement 81.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat room temperature
  2. 2
    Autrefor 2 hr
  3. 3
    FiltrationPd/C was filtered off through a pad of celite
  4. 4
    Concentrationthe mother liquid was concentrated

Mode opératoire

Mixture (6) (2.3 g) was hydrogenated in MeOH (50 mL) using Pd/C (10%, dry, 200 mg) and H2 balloon at 1 atm at room temperature for 2 hr. Pd/C was filtered off through a pad of celite and the mother liquid was concentrated to give Compound 2 as white solid (1.13 g, 81%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09120745B2uspto-grants-2015_09