Reaction #1183627
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US06075029
Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of furfurylurea (7.0 g, 50.0 mmol), cyanoacetic acid (4.7 g, 55.0 mmol), and acetic anhydride (50 ml) was heated to 95° C. for 3 hours. After cooling to ambient temperature the solution was concentrated under reduced pressure to give a crude intermediate that was stirred with water (30 ml). After concentrating, the residue was dissolved in water (100 ml) and treated with a 50% aqueous sodium hydroxide solution (10 ml) to give a pH of 13. This solution was heated at 70° C. for 30 minutes, cooled and filtered. The wet solids were stirred in boiling ethanol for 15 minutes, cooled to ambient temperature and filtered. The filtrate was evaporated under reduced pressure to give 6-amino-1-furfuryluracil (5.5 g, 53% yield) as an orange solid. was concentrated under reduced pressure to give a crude intermediate After concentrating the residue was dissolved in water (100 ml) treated with a 50% aqueous sodium hydroxide solution (10 ml) to give a pH of 13 This solution was heated at 70° C. for 30 minutes cooled filtered for 15 minutes cooled to ambient temperature filtered The filtrate was evaporated under reduced pressure
Source ID: ord-8283b5e8dd554cfe92b7ef602c0459eb