HRID1655260

反应详情

EQUATION

反应方程式

HRID 1655260 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 5-(2-allyloxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (0.25 g, 0.0008 mol), phenol (0.145 g, 0.0015 mol), piperidine (0.131 g, 0.0015 mol) and tetrakis(triphenylphosphine)palladium(0) (0.046 g, 0.00004 mol) in absolute ethanol (5ml) was refluxed overnight under nitrogen. The mixture was allowed to cool, the solvent evaporated under vacuum and the residue dissolved in ethyl acetate (40 ml). This solution was washed with water (3×10 ml), 1M HCl (3×10 ml) and brine (1×10 ml). After drying (Na2SO4) and filtration, the filtrate was evaporated under vacuum to give the crude product. The title phenol (0.021 g, 10%) was obtained after trituration with diethyl ether and crystallisation from ethyl acetate/pentane, m.p. 233°-238° C. Found: C,63.17; H,5.65; N,19.52. C15H16N4O2 requires C,63.36; H,5.67; N,19.71%.

WORKUP

后处理

  1. temperaturewas refluxed overnight under nitrogen
  2. temperatureto cool
  3. customthe solvent evaporated under vacuum
  4. dissolutionthe residue dissolved in ethyl acetate (40 ml)
  5. washThis solution was washed with water (3×10 ml), 1M HCl (3×10 ml) and brine (1×10 ml)
  6. customAfter drying
  7. filtration(Na2SO4) and filtration
  8. customthe filtrate was evaporated under vacuum
  9. customto give the crude product