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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081650Generated: October 27, 2026

Carbonic acid-guanidine (1:1) → 2-amino-6-ethyl-5-(3-undecylphenoxy)-1H-pyrimidin-4-one

https://huagongshe.com/reaction/1081650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic acid-guanidine (1:1)HCID 286947—
ReactantEthyl 2-(3-undecylphenoxy)-3-oxopentanoateHCID 19955508—
SolventEthanolHCID 702—
Product2-amino-6-ethyl-5-(3-undecylphenoxy)-1H-pyrimidin-4-oneHCID 17844280615.7%

Reaction Steps

A stirred solution of 8.9 grams (0.028 mole) of ethyl 2-(3-undecylphenoxy)-3-oxopentanoate and 2.5 grams (0.028 mole) of guanidine carbonate in 30 mL of ethanol was heated at reflux for about 6 hours. The reaction mixture was then concentrated under reduced pressure to a residue. The residue was taken up in 50 mL of water and 5 mL of acetic acid, and the mixture was extracted with 50 mL of diethyl ether. The ether layer was extracted with 20 grams of aqueous 10% sodium hydroxide and then with 100 mL of water. The water extract was made acidic with acetic acid, and then it was extracted with 50 mL of diethyl ether. The ether extract was concentrated under reduced pressure to a residue. The residue was then taken up in 25 mL of heptane, and the mixture was again concentrated under reduced pressure to a residual solid. The solid was slurried in an additional 25 mL of heptane, and then it was collected by filtration. The solid was dried under reduced pressure, yielding 1.7 grams of 2-amino-6-ethyl-4-hydroxy-5-(3-undecylphenoxy)pyrimidine. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587379
Source datasetuspto-grants-1996_12
ORD IDord-bb7e1a49282045ec910e8a7bed4849f6
Source noteuspto-grants-1996_12