Ethanol → 1H-Purine-2,6-dione, 3,7-dihydro-3-(2,2-dimethylpropyl)-
Reaction equation
[NH2:1][C:2]1[C:3](=[O:15])[NH:4][C:5](=[O:14])[N:6]([CH2:9][C:10]([CH3:13])([CH3:12])[CH3:11])[C:7]=1[NH2:8].[CH2:16](O)C>C(N)=O>[CH3:13][C:10]([CH3:11])([CH3:12])[CH2:9][N:6]1[C:7]2[N:8]=[CH:16][NH:1][C:2]=2[C:3](=[O:15])[NH:4][C:5]1=[O:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.0 g of XXVIII was refluxed in 20 ml of formamide for 30 minutes. After cooling 30 ml of ethanol was added and the yellow crystals were filtered off and recrystallized from 15 ml of DMF. Yield 2.0 g (XXIX) NMR (see Table I).
Workup
- additionwas added
- filtrationthe yellow crystals were filtered off
- customrecrystallized from 15 ml of DMF
Sources & evidence
- ORD record
- ord-c92df7b19c854ad7a9369a3af5c847ca
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04644001
Reaction notes
Loading…