HCID 10998089, compound → 6-Amino-1-phenyl-1H-pyrimidine-2,4-dione
Reaction equation
[C:1]([CH2:3][C:4]([NH:6][C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:8])=[O:5])#[N:2]>[OH-].[Na+]>[NH2:2][C:1]1[N:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[C:7](=[O:8])[NH:6][C:4](=[O:5])[CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
1-(2-Cyano-acetyl)-3-phenyl-urea (12.6 g, 62.1 mmol) was taken in 50 ml 2M sodium hydroxide (aq.) and stirred at room temperature for 2 h under LC-MS control. After cooling down by immersing in ice bath and neutralization with acetic acid and thus formed solids were separated by filtration, washed well with ice cold water and dried under high vacuum yielding white solids (11.9 g, 58.6 mmol, 94.4%).
Workup
- temperatureAfter cooling down
- customneutralization with acetic acid and thus formed solids were separated by filtration
- washwashed well with ice cold water
- customdried under high vacuum
Sources & evidence
- ORD record
- ord-1ecfc30e30ac4cfeb10b1bd63882eb4d
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08629272B2
Reaction notes
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