Water → 5-(2-Allyloxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one
Reaction equation
[CH2:1]([O:4][C:5]1[CH:25]=[CH:24][CH:23]=[CH:22][C:6]=1[C:7]([NH:9][C:10]1[C:11]([CH2:19][CH2:20][CH3:21])=[N:12][N:13]([CH3:18])[C:14]=1[C:15]([NH2:17])=[O:16])=O)[CH:2]=[CH2:3].[OH-].[Na+].O>C(O)C>[CH2:1]([O:4][C:5]1[CH:25]=[CH:24][CH:23]=[CH:22][C:6]=1[C:7]1[NH:17][C:15](=[O:16])[C:14]2[N:13]([CH3:18])[N:12]=[C:11]([CH2:19][CH2:20][CH3:21])[C:10]=2[N:9]=1)[CH:2]=[CH2:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-(2-allyloxybenzamido)-1-methyl-3-n-propylpyrazole-5-carboxamide (1.2 g, 0.0035 mol), sodium hydroxide (0.70 g, 0.018 mol), water (34 ml) and ethanol (8 ml) was refluxed for 5 hours. After cooling, the solution was exhaustively extracted with ethyl acetate. The combined extracts were washed with brine (30 ml), dried (Na2SO4), filtered and the solvent evaporated under vacuum to give a crude product which was crystallised from ethyl acetate/hexane to afford the title compound (0.476 g, 37%), m.p. 116°-119° C. Found: C,67.00; H,6.21; N,17.23. C18H20N4O2 requires C,66.65; H,6.21; N,17.27%.
Workup
- temperaturewas refluxed for 5 hours
- temperatureAfter cooling
- extractionthe solution was exhaustively extracted with ethyl acetate
- washThe combined extracts were washed with brine (30 ml)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customthe solvent evaporated under vacuum
- customto give a crude product which
- customwas crystallised from ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-e1f113e8d9fa42478c225361a5ab4ca4
- Source dataset
- uspto-grants-1993_10
- Patent number
- US05250534
Reaction notes
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