Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324784Generated: October 26, 2026

Acetic Acid → 3-Phenylpropyl 2-(2-furyl)-4-(4-methyl-3-nitrophenyl)-6[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/324784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMorpholineHCID 8083—
ReactantSodium SulfateHCID 24436—
Reactant3-Nitro-p-tolualdehydeHCID 1798998—
ReactantFuran-2-carboximidamide hydrochlorideHCID 12231049—
Reactant3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
SolventEthanolHCID 702—
Product3-Phenylpropyl 2-(2-furyl)-4-(4-methyl-3-nitrophenyl)-6[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylateHCID 220055320.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (10.0 g, 28.78 mmol), 4-methyl-3-nitrobenzaldehyde (4.75 g, 28.78 mmol), 2-amidinofuran hydrochloride (4.20 g, 28.78 mmol), morpholine (3.75 ml, 43.17 mmol), acetic acid (3.29 ml, 57.56 mmol), and sodium sulfate (8.17 g, 57.56 mmol) was stirred in ethanol (50 ml) for 1 hour at room temperature and then heated to 50° C. for 7 days. The ethanol was removed in vacuo and ethyl acetate was added to the residue. The mixture was filtered and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. The oil was further purified by flash chromatography and RP-HPLC (twice) to give the title compound (150 mg) as an oil. Electrospray MS m/z 587 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218538B1
Source datasetuspto-grants-2001_04
ORD IDord-25ce43649d774d819074daa971a8dfd7
Source noteuspto-grants-2001_04