Water → 5-(2-Allyloxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one

HRID 862900Notes

Reaction equation

HRID 862900 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

Procedure

A mixture of 4-(2-allyloxybenzamido)-1-methyl-3-n-propyl-pyrazole-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

  1. temperaturewas refluxed for 5 hours
  2. temperatureAfter cooling
  3. extractionthe solution was exhaustively extracted with ethyl acetate
  4. washThe combined extracts were washed with brine (30 ml)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customthe solvent evaporated under vacuum
  8. customto give a crude product which
  9. customwas crystallised from ethyl acetate/hexane

Sources & evidence

ORD record
ord-2c84483ece9645b487e8dc13b885761e
Source dataset
uspto-grants-1998_02
Patent number
US05719283

Reaction notes

Loading…