HCID 135736201, compound → 8-(2-Dimethylamino-4-nitro-phenyl)purin-6-one
Reaction equation
[NH2:1][C:2]1[C:7](=[O:8])[NH:6][CH:5]=[N:4][C:3]=1[NH:9][C:10](=O)[C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:12]=1[N:20]([CH3:22])[CH3:21]>C(O)(=O)C>[CH3:21][N:20]([CH3:22])[C:12]1[CH:13]=[C:14]([N+:17]([O-:19])=[O:18])[CH:15]=[CH:16][C:11]=1[C:10]1[N:1]=[C:2]2[C:3](=[N:4][CH:5]=[N:6][C:7]2=[O:8])[N:9]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
One gram of 5-amino-4-(2-dimethylamino-4-nitro-benzoylamino)pyrimidin-6-one is refluxed for two hours in 50 ml of glacial acetic acid. The mixture is evaporated to dryness, and the residue is stirred out with ethanol in the warm.
Workup
- customThe mixture is evaporated to dryness
Sources & evidence
- ORD record
- ord-cd16ce517d74444e9c3738b0eac46728
- Source dataset
- uspto-grants-1988_02
- Patent number
- US04722929
Reaction notes
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