Hydrochloric Acid → HCID 10536497, compound
Reaction equation
[NH2:1][C:2]1[N:7]([CH2:8][CH:9]([CH3:11])[CH3:10])[C:6](=[O:12])[NH:5][C:4](=[O:13])[CH:3]=1.Cl.[N:15]([O-])=[O:16].[Na+]>O>[NH2:1][C:2]1[N:7]([CH2:8][CH:9]([CH3:11])[CH3:10])[C:6](=[O:12])[NH:5][C:4](=[O:13])[C:3]=1[N:15]=[O:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To 44.7 g (0.24 mol) of 6-amino-1-(2-methylpropyl)-2,4-(1H,3H)-pyrimidinedione (XIV), dissolved in 2 l hot water, was added 50 ml of 5 N HCl and 17 g of NaNO2 (0.25 mol) which were dissolved in water. After cooling the red crystals were filtered off and washed with water. Yield 44.6 g (95%) (XV), NMR.
Workup
- temperatureAfter cooling the red crystals
- filtrationwere filtered off
- washwashed with water
Sources & evidence
- ORD record
- ord-d06afdd8fc1040b59a5c88866242821d
- Source dataset
- uspto-grants-1982_04
- Patent number
- US04325956
Reaction notes
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