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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655260Generated: November 1, 2026

Phenol → 1,6-Dihydro-5-(2-hydroxyphenyl)-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/1655260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPiperidineHCID 8082—
Reactant5-(2-Allyloxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-oneHCID 135738548—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product1,6-Dihydro-5-(2-hydroxyphenyl)-1-methyl-3-propyl-7H-pyrazolo[4,3-d]pyrimidin-7-oneHCID 13554651710%

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250534
Source datasetuspto-grants-1993_10
ORD IDord-4ab1addfa8984f38940bddadf09065ee
Source noteuspto-grants-1993_10