5-prop-2-enyl-1H-pyrimidine-2,4-dione → HCID 14914594, compound
Reaction equation
[CH2:1]([C:4]1[C:5](=[O:11])[NH:6][C:7](=[O:10])[NH:8][CH:9]=1)[CH:2]=[CH2:3]>CCO>[CH:1](/[C:4]1[C:5](=[O:11])[NH:6][C:7](=[O:10])[NH:8][CH:9]=1)=[CH:2]\[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 5-allyluracil (80 mg; 0.5 mmol) in 95% aq. EtOH (50 ml) was added (Ph3P)3RhCl (90 mg; 0.1 mmol) and the mixture heated under reflux for 3 days. The solvent was evaporated and the product isolated by flash chromatography on SiO2 eluted with 5% MeOH-CH2Cl2. Yield 56 mg 70%; 200 MHz 1H-NMR DMSO-d6, δ:11.0 (br s, 1H, NH); 7.42 (s, 1H, 6-H); 6.35-6.55 (qq, 1H =CH--Me); 5.95-6.1 (dd, 1H, --CH=); 1.74 (dd, 3H, CH3).
Workup
- temperaturethe mixture heated
- temperatureunder reflux for 3 days
- customThe solvent was evaporated
- customthe product isolated by flash chromatography on SiO2
- washeluted with 5% MeOH-CH2Cl2
Sources & evidence
- ORD record
- ord-7352fa23049b49a9b741f8bdc5d9dc3e
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05356882
Reaction notes
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