Reaktion #159872
ord-86cd04daa4e24f2dad931c11784256e7
Reaktionsgleichung
Phenyl isothiocyanate
6-hydrazinyl-1-(4-methoxybenzyl)-3-methylpyrimidine-2,4(1H,3H)-dione
→
product
7-(4-Methoxybenzyl)-5-methyl-3-(phenylamino)-1H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeevaporated
- 2Sonstigeto remove solvent under reduced pressure
- 3WaschenThe residue is washed with hexanes
- 4workup.ADDITIONtreated with MeOH (125 mL)
- 5Sonstigeto give a crystalline solid
- 6SonstigeThe solid is recrystallized from CH3OH-EtOAc
Vorschrift
Phenyl isothiocyanate (3.9 mL, 32.7 mmol) is added to a suspension of 6-hydrazinyl-1-(4-methoxybenzyl)-3-methylpyrimidine-2,4(1H,3H)-dione (0.45 g, 1.6 mmol) in DMF (12 mL). The reaction mixture is heated at 120° C. for 40 hours, and then evaporated to remove solvent under reduced pressure. The residue is washed with hexanes, and then treated with MeOH (125 mL), and stored at −15° C. for 2 days to give a crystalline solid. The solid is recrystallized from CH3OH-EtOAc to afford 2.5 g of product (Yield: 61%). 1H NMR (400 MHz, DMSO-d6) δ3.21 (s, 3H), 3.73 (s, 3H), 5.01 (s, 2H), 6.88-7.36 (m, 9H). MS (FAB) m/z 378.3 [M+H]+.