Sodium Hydroxide → HCID 178524765, compound
Reaction equation
[CH2:1]([NH:7][C:8]1[N:13]=[C:12]([OH:14])[C:11]([C:15]([O:17]CC)=[O:16])=[CH:10][N:9]=1)[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>O>[CH2:1]([NH:7][C:8]1[N:13]=[C:12]([OH:14])[C:11]([C:15]([OH:17])=[O:16])=[CH:10][N:9]=1)[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Furfurylamino-5-ethoxycarbonyl-4-hydroxypyrimidine (526 mg, 2 mmol) was hydrolysed in water (10 ml) with NaOH (5 mmol, 200 mg) by refluxing for 3 h. Cooling and acidification to pH 2 yielded the named product as a precipitate. (435 mg, 93% yield).
Workup
- temperatureby refluxing for 3 h
- temperatureCooling
- customacidification to pH 2 yielded the named product as a precipitate
Sources & evidence
- ORD record
- ord-3ff1f23703f8428eaa9c0fadcbfee765
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04447422
Reaction notes
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