HCID 178439465, compound → HCID 178439466, compound
Reaction equation
[O:1]=[C:2]1[N:7]([CH2:8][C:9]([O:11]C)=[O:10])[C:6](=[O:13])[CH:5]=[C:4]([CH2:14][CH2:15][CH3:16])[N:3]1[CH2:17][C:18]1[CH:23]=[CH:22][C:21]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:30]2[NH:34][N:33]=[N:32][N:31]=2)=[CH:20][CH:19]=1>CO.[OH-].[Na+]>[O:1]=[C:2]1[N:7]([CH2:8][C:9]([OH:11])=[O:10])[C:6](=[O:13])[CH:5]=[C:4]([CH2:14][CH2:15][CH3:16])[N:3]1[CH2:17][C:18]1[CH:23]=[CH:22][C:21]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[C:30]2[NH:34][N:33]=[N:32][N:31]=2)=[CH:20][CH:19]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of methyl 2,4-dioxo-6-propyl-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1,2,3,4-tetrahydropyrimidine-3-acetate (0.25 g) in methanol (10 ml) and 1N sodium hydroxide (1.5 ml) was heated under reflux for 16 hours. The reaction solution was evaporated to dryness and the residue was dissolved in water. The solution was acidified with 1N hydrochloric acid to give a crystalline product (0.19 g, 79%).
Workup
- temperaturewas heated
- temperatureunder reflux for 16 hours
- customThe reaction solution was evaporated to dryness
- dissolutionthe residue was dissolved in water
Sources & evidence
- ORD record
- ord-eba49f7946f64a158a260a09a50b808d
- Source dataset
- uspto-grants-1992_11
- Patent number
- US05162326
Reaction notes
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