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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210487Generated: October 30, 2026

4-[3-(Bicyclo[2.2.1]hept-2-yloxy)-4-Methoxyphenyl]-4-Hydroxy-1,2,3,4-Tetrahydro-2-Pyrimidinone → HCID 178488672, compound

https://huagongshe.com/reaction/2210487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(Bicyclo[2.2.1]hept-2-yloxy)-4-Methoxyphenyl]-4-Hydroxy-1,2,3,4-Tetrahydro-2-PyrimidinoneHCID 14010186—
SolventEthanolHCID 702—
ProductHCID 178488672HCID 17848867231.5%

Reaction Steps

The hydroxy pyrimidinone of Example 60 (0.2 g, 0.61 mmol) is dissolved in 5 ml ethanol, treated with 2.5 ml 1N HC1 and refluxed for 6 hours. The reaction is cooled to room temperature, quenched with water and the product extracted 3x ethyl acetate. The organics are washed, dried, filtered and concentrated in vacuo to yield a crude substance which is crystallized from ethyl acetate to give 60 mg (31.5%) of the pyrimidinone as a crystalline solid. This material is a 7:3 mixture of endo-exo bicycloalkyl isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459145
Source datasetuspto-grants-1995_10
ORD IDord-f7145ebc684043138c3b7daa780d0f6c
Source noteuspto-grants-1995_10